Rekambys Epar Product Information - en PDF

ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
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1. NAME OF THE MEDICINAL PRODUCT
REKAMBYS 600 mg prolonged-release suspension for injection

2. QUALITATIVE AND QUANTITATIVE COMPOSITION
2 mL vial
Each vial contains 600 mg rilpivirine
3 mL vial
Each vial contains 900 mg rilpivirine
For the full list of excipients, see section 6.1.
3. PHARMACEUTICAL FORM
Prolonged-release suspension for injection

White to off-white suspension.
4. CLINICAL PARTICULARS
4.1 Therapeutic indications
REKAMBYS is indicated, in combination with cabotegravir injection, for the treatment of human
immunodeficiency virus type 1 (HIV-1) infection in adults who are virologically suppressed (HIV-1
RNA < 50 copies/mL) on a stable antiretroviral regimen without present or past evidence of viral
resistance to, and no prior virological failure with, agents of the NNRTI and INI class (see
sections 4.2, 4.4 and 5.1).
4.2 Posology and method of administration
Therapy should be prescribed by a physician experienced in the management of HIV infection. Each
injection should be administered by a healthcare professional.
Prior to starting REKAMBYS, the healthcare professional should carefully select patients who
agree to the required injection schedule and counsel patients about the importance of adherence
to scheduled dosing visits to help maintain viral suppression and reduce the risk of viral
rebound and potential development of resistance associated with missed doses.
Following discontinuation of REKAMBYS in combination with cabotegravir injection, it is

essential to adopt an alternative, fully suppressive antiretroviral regimen no later than one
month after the last every 1 month injection of REKAMBYS or two months after the last every
2 months injection of REKAMBYS (see section 4.4).
The prescribing information for cabotegravir injection should be consulted for recommended dosing.
Posology
Oral lead-in
Prior to the initiation of REKAMBYS, rilpivirine oral tablets, together with cabotegravir oral tablets,
should be taken for approximately 1 month (at least 28 days) to assess tolerability to rilpivirine and
cabotegravir (see section 4.4). One rilpivirine 25-mg tablet should be taken with a meal with one
cabotegravir 30-mg tablet once daily.
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Every 1 month dosing
Initiation injection (900 mg corresponding to 3 mL)
On the final day of oral lead-in, the recommended initiation injection dose of rilpivirine in adults is a
single 900 mg intramuscular injection.
Continuation injection (600 mg corresponding to 2 mL)

After the initiation injection, the recommended continuation injection dose of rilpivirine in adults is a
single 600 mg monthly intramuscular injection. Patients may be given injections up to 7 days before or
after the date of the monthly injection schedule.
Table 1: Recommended oral lead-in and monthly dosing schedule in adult patients
Oral IM IM
Lead-In Initiation injections Continuation injections
Medicinal During month 1
At month 2 month 3 onwards
Product (at least 28 days)
Rilpivirine 25 mg once daily 900 mg 600 mg monthly
Cabotegravir 30 mg once daily 600 mg 400 mg monthly
IM=Intramuscular injection.
Every 2 months dosing

Initiation Injections –1 month apart (900 mg corresponding to 3 mL)
On the final day of oral lead-in, the recommended initial rilpivirine injection dose in adults is a single
900 mg intramuscular injection (month 2).
One month later (month 3), a second 900 mg intramuscular injection should be administered. Patients
may be given the second 900 mg injection up to 7 days before or after the scheduled dosing date.
Continuation Injections – 2 months apart (900 mg corresponding to 3 mL)

After the initiation injections, the recommended rilpivirine continuation injection dose in adults is a
single 900 mg intramuscular injection administered every 2 months beginning at month 5. Patients
may be given injections up to 7 days before or after the date of the every 2 months injection schedule.
Table 2: Recommended oral lead-in and every 2 months dosing schedule in adult patients
Oral IM IM
Lead-In Initiation injections Continuation injections
Medicinal During month 1 At month 2 and month 3 month 5 onwards
Product (at least 28 days)
Rilpivirine 25 mg once daily 900 mg monthly 900 mg every 2 months
Cabotegravir 30 mg once daily 600 mg monthly 600 mg every 2 months
Dosing Recommendations When Switching From Monthly to Every 2 Months Injections

Patients switching from a monthly continuation injection schedule to an every 2 months continuation
injection schedule should receive a single 900 mg intramuscular injection of REKAMBYS one month
after the last 600 mg REKAMBYS continuation injection dose and then 900 mg every 2 months
thereafter.
Dosing Recommendations When Switching From Every 2 Months to Monthly Injections

Patients switching from an every 2 months continuation injection schedule to a monthly continuation
injection schedule should receive a single 600 mg intramuscular injection of REKAMBYS
two months after the last 900 mg REKAMBYS continuation injection dose and then 600 mg monthly
thereafter.
Missed doses
Patients who miss an injection visit should be clinically reassessed to ensure resumption of therapy is
appropriate. See Table 3 and 4 for dosing recommendations after a missed injection.
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Missed every 1 month injection (Oral Dosing to Replace Up to 2 Consecutive Monthly Injections)
If a patient plans to miss a scheduled injection by more than 7 days, daily oral therapy (one rilpivirine
tablet [25 mg] and one cabotegravir tablet [30 mg]) may be used to replace up to 2 consecutive
monthly injection visits. The first dose of oral therapy should be taken 1 month (± 7 days) after the last
injection doses of REKAMBYS and cabotegravir. Injection dosing should be resumed on the day oral
dosing completes, as recommended in Table 3.
In case more than two months need to be covered for, ie, missing more than two monthly injections, an
alternative oral regimen should be initiated one month (± 7 days) after the final injection of
REKAMBYS.
Table 3: REKAMBYS dosing recommendations after missed injections or oral therapy for
patients on monthly injection dosing
Time since last injection Recommendation
≤ 2 months: Continue with the monthly 600 mg injection schedule as soon as
possible.
> 2 months: Re-initiate the patient on the 900 mg dose, and then continue to follow
the monthly 600 mg injection schedule.
Missed every 2 months injection (Oral Dosing to Replace 1 Every 2 Months Injection)
If a patient plans to miss a scheduled injection visit by more than 7 days, daily oral therapy (one
rilpivirine tablet [25 mg] and one cabotegravir tablet [30 mg]) may be used to replace one ‘every
2 months’ injection visit. The first dose of oral therapy should be taken approximately two months
(±7 days) after the last injection doses of REKAMBYS and cabotegravir. Injection dosing should be
resumed on the day oral dosing completes, as recommended in Table 4.
In case more than two months need to be covered for, ie, missing more than one ‘every 2 months’
injection, an alternative oral regimen should be initiated two months (± 7 days) after the final injection
of REKAMBYS.
Table 4: REKAMBYS dosing recommendations after missed injections or oral therapy for
patients on every 2 months injection dosing
Missed Injection Time since Recommendation (all injections are 3 mL)
Visit last injection
Injection 2 ≤ 2 months Continue with the 900 mg injection as soon as possible and
(month 3) continue with every 2 months injection schedule.
> 2 months Re-initiate the patient on the 900 mg dose, followed by a
second 900 mg initiation injection one month later. Then
follow the every 2 months injection schedule.
Injection 3 or ≤ 3 months Continue with the 900 mg injection as soon as possible and
later (month 5 continue with every 2 months injection schedule.
onwards) > 3 months Re-initiate the patient on the 900 mg dose, followed by a
second 900 mg initiation injection one month later. Then
follow the every 2 months injection schedule.
Special populations
Elderly
There is limited information regarding the use of REKAMBYS in patients > 65 years of age. No dose
adjustment of REKAMBYS is required in older patients (see sections 5.1 and 5.2).
Renal impairment
No dose adjustment is required in patients with mild or moderate renal impairment. In patients with
severe renal impairment or end stage renal disease, the combination of REKAMBYS with a strong
CYP3A inhibitor should only be used if the benefit outweighs the risk. Subjects with estimated
creatinine clearance < 50 mL/min/1.73 m2 were not included in the Phase 3 studies. No data are
available in subjects receiving dialysis although differences in pharmacokinetics are not expected in
this population (see section 5.2).
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Hepatic impairment
No dose adjustment is required in patients with mild or moderate hepatic impairment (Child-Pugh
score A or B), but caution is advised in patients with moderate hepatic impairment. No data are
available in patients with severe hepatic impairment (Child-Pugh score C); therefore REKAMBYS is
not recommended in these patients (see section 5.2).
Paediatric population
The safety and efficacy of REKAMBYS in children and adolescents aged < 18 years have not been
established. No data are available.
Method of administration
For intramuscular use.

Care should be taken to avoid inadvertent injection of REKAMBYS into a blood vessel.
REKAMBYS should be administered by a healthcare professional. For instructions on administration,

see “Instructions for Use” in the package leaflet.
REKAMBYS should always be co-administered with a cabotegravir injection. REKAMBYS and

cabotegravir injections should be administered at separate gluteal injection sites during the same visit.
The order of injections is not important.
When administering REKAMBYS, the healthcare professional should take into consideration the body
mass index (BMI) of the patient to ensure that the needle length is sufficient to reach the gluteus
muscle. The pack contains 1 injection needle (see section 6.5).
The vial should be held firmly and shaken vigorously for a full 10 seconds. The vial should be inverted
and the resuspension should be checked. It should look uniform. If the suspension is not uniform, the
vial should be shaken again. It is normal to see small air bubbles.
Injections must be administered to the ventrogluteal (recommended) or the dorsogluteal sites.
4.3 Contraindications
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
REKAMBYS must not be co-administered with the following medicinal products, as significant
decreases in rilpivirine plasma concentrations may occur (due to CYP3A enzyme induction), which
may result in loss of therapeutic effect of REKAMBYS (see section 4.5):
- the anticonvulsants carbamazepine, oxcarbazepine, phenobarbital, phenytoin
- the antimycobacterials rifabutin, rifampicin, rifapentine
- the systemic glucocorticoid dexamethasone, except as a single dose treatment
- St John’s wort (Hypericum perforatum).
4.4 Special warnings and precautions for use
Risk of resistance following treatment discontinuation
To minimise the risk of developing viral resistance it is essential to adopt an alternative, fully
suppressive antiretroviral regimen no later than one month after the last every 1 month
injection of REKAMBYS or two months after the last every 2 months injection of REKAMBYS.
If virologic failure is suspected, an alternative regimen should be adopted as soon as possible.
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Long-acting properties of rilpivirine injection
Residual concentrations of rilpivirine may remain in the systemic circulation of patients for prolonged
periods (up to 4 years in some patients) and should be considered upon discontinuation of
REKAMBYS (see sections 4.5, 4.6, 4.7, 4.9).
Baseline factors associated with virological failure
Before starting the regimen, it should be taken into account that multivariable analyses indicate that a
combination of at least 2 of the following baseline factors may be associated with an increased risk of
virological failure: archived rilpivirine resistance mutations, HIV-1 subtype A6/A1, or BMI
≥ 30 kg/m2. In patients with an incomplete or uncertain treatment history without pre-treatment
resistance analyses, caution is warranted in the presence of either BMI ≥ 30 kg/m2 or HIV-1 subtype
A6/A1 (see section 5.1).
Post-injection reactions
Partial intravenous administration may result in AEs due to temporarily high plasma concentrations. In
clinical studies, serious post-injection reactions were reported within minutes after the injection of
rilpivirine, including dyspnoea, agitation, abdominal cramping, flushing, sweating, oral numbness, and
changes in blood pressure. These events were very rare and began to resolve within a few minutes
after the injection.
Carefully follow the Instructions for Use when preparing and administering REKAMBYS to avoid
accidental intravenous administration. Observe patients briefly (approximately 10 minutes) after the
injection. If a patient experiences a post-injection reaction, monitor and treat as clinically indicated.
Cardiovascular
REKAMBYS should be used with caution when co-administered with a medicinal product with a
known risk of Torsade de Pointes. At supra-therapeutic doses (75 and 300 mg once daily), oral
rilpivirine has been associated with prolongation of the QTc interval of the electrocardiogram (ECG)
(see sections 4.5, 4.8 and 5.2). Oral rilpivirine at the recommended dose of 25 mg once daily is not
associated with a clinically relevant effect on QTc. Plasma rilpivirine concentrations after
REKAMBYS injections are comparable to those during such oral rilpivirine therapy.
HBV/HCV co-infection
Patients with hepatitis B co-infection were excluded from studies with REKAMBYS. It is not
recommended to initiate REKAMBYS in patients with hepatitis B co-infection. In patients co-infected
with hepatitis B receiving oral rilpivirine, the incidence of hepatic enzyme elevation was higher than
in patients receiving oral rilpivirine who were not hepatitis B co-infected. Physicians should refer to
current treatment guidelines for the management of HIV infection in patients co-infected with hepatitis
B virus.
Limited data is available in patients with hepatitis C co-infection. In patients co-infected with hepatitis
C receiving oral rilpivirine, the incidence of hepatic enzyme elevation was higher than in patients
receiving oral rilpivirine who were not hepatitis C co-infected. The pharmacokinetic exposure of oral
and injectable rilpivirine in co-infected patients was comparable to that in patients without hepatitis C
co-infection. Monitoring of liver function is recommended in patients with hepatitis C co-infection.
Interactions with other medicinal products
REKAMBYS should not be administered with other antiretroviral medicinal products, except for
cabotegravir injection for the treatment of HIV-1 infection (see section 4.5).
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Pregnancy
There are limited data of REKAMBYS in pregnant women. REKAMBYS is not recommended during
pregnancy unless the expected benefit justifies the potential risk. Lower exposures of oral rilpivirine
were observed when rilpivirine 25 mg once daily was taken during pregnancy. In the Phase 3 studies
with oral rilpivirine, lower rilpivirine exposure, similar to that seen during pregnancy, has been
associated with an increased risk of virological failure, therefore viral load should be monitored
closely. Alternatively, switching to another ART regimen could be considered (see sections 4.6, 5.1
and 5.2).
Immune reactivation syndrome
In HIV-infected patients with severe immune deficiency at the time of institution of combination
antiretroviral therapy (CART), an inflammatory reaction to asymptomatic or residual opportunistic
pathogens may arise and cause serious clinical conditions, or aggravation of symptoms. Typically,
such reactions have been observed within the first few weeks or months of initiation of CART.
Relevant examples are cytomegalovirus retinitis, generalised and/or focal mycobacterial infections,
and Pneumocystis jirovecii pneumonia. Any inflammatory symptoms should be evaluated and
treatment instituted when necessary. Autoimmune disorders (such as Graves’ disease and autoimmune
hepatitis) have also been reported to occur in the setting of immune reconstitution, however, the
reported time to onset is more variable and these events can occur many months after initiation of
treatment.
Transmission of HIV
While effective viral suppression with antiretroviral therapy has been proven to substantially reduce
the risk of sexual transmission, a residual risk cannot be excluded. Precautions to prevent transmission
should be taken in accordance with national guidelines.
Opportunistic infections
Patients should be advised that REKAMBYS or any other antiretroviral therapy does not cure HIV
infection and that they may still develop opportunistic infections and other complications of HIV
infection. Therefore, patients should remain under close clinical observation by physicians
experienced in the treatment of these associated HIV diseases.
Excipients
This medicine contains less than 1 mmol sodium (23 mg) per injection, that is to say essentially
‘sodium-free’.
4.5 Interaction with other medicinal products and other forms of interaction
REKAMBYS, in combination with cabotegravir injection, is intended for use as a complete regimen
for the treatment of HIV-1 infection and should not be administered with other antiretroviral medicinal
products for the treatment of HIV-1. Therefore, information regarding drug-drug interactions with
other antiretroviral medicinal products is not provided. From a drug interaction perspective, there are
no limitations on the use of other antiretroviral medicinal products after discontinuing REKAMBYS.
For the oral lead-in rilpivirine treatment and in case missed doses are replaced by oral rilpivirine
treatment, refer to the oral rilpivirine tablet SmPC for information about drug interactions.
Medicinal products that affect rilpivirine exposure
Rilpivirine is primarily metabolised by cytochrome P450 (CYP)3A. Medicinal products that induce or
inhibit CYP3A may thus affect the clearance of rilpivirine (see section 5.2). Co-administration of
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rilpivirine and medicinal products that induce CYP3A has been observed to decrease the plasma
concentrations of rilpivirine, which could reduce the therapeutic effect of rilpivirine.
Co-administration of rilpivirine and medicinal products that inhibit CYP3A has been observed to
increase the plasma concentrations of rilpivirine.
When using oral rilpivirine, proton pump inhibitors are contraindicated (see rilpivirine tablet SmPC,
section 4.3).
Medicinal products that are affected by the use of rilpivirine
Rilpivirine is not likely to have a clinically relevant effect on the exposure of medicinal products
metabolised by CYP enzymes.
Rilpivirine inhibits P-glycoprotein in vitro (IC50 is 9.2 μM). In a clinical study, oral rilpivirine (25 mg
once daily) did not significantly affect the pharmacokinetics of digoxin.
Rilpivirine is an in vitro inhibitor of the transporter MATE-2K with an IC50 of < 2.7 nM. The clinical
implications of this finding are currently unknown.
Interaction table
Selected established and theoretical interactions between rilpivirine and co-administered medicinal
products are listed in Table 5 and are based on the studies conducted with oral rilpivirine or are
potential drug interactions that may occur (increase is indicated as “↑”, decrease as “↓”, no change as
“↔”, not applicable as “NA”, confidence interval as “CI”).
Table 5: Interactions and dose recommendations with other medicinal products

Medicinal products by Interaction Recommendations concerning
therapeutic areas Geometric mean change (%)Ω co-administration
ANTIVIRAL AGENTS
Cabotegravir cabotegravir AUC ↔ No dose adjustment is required.
cabotegravir Cmin↔
cabotegravir Cmax ↔
rilpivirine AUC ↔
rilpivirine Cmin ↓ 8%
rilpivirine Cmax ↔
Ribavirin Not studied. No clinically relevant No dose adjustment is required.
drug-drug interaction is expected.
ANTICONVULSANTS
Carbamazepine Not studied. Significant decreases in Rilpivirine must not be used in
Oxcarbazepine rilpivirine plasma concentrations are combination with these
Phenobarbital expected. anticonvulsants as
Phenytoin co-administration may result in loss
(induction of CYP3A enzymes) of therapeutic effect of rilpivirine
(see section 4.3).
AZOLE ANTIFUNGAL AGENTS
Ketoconazole*# ketoconazole AUC ↓ 24% No dose adjustment is required.
400 mg once daily ketoconazole Cmin ↓ 66%
ketoconazole Cmax ↔
(induction of CYP3A due to high

rilpivirine dose in the study)
rilpivirine AUC ↑ 49%

rilpivirine Cmin ↑ 76%
rilpivirine Cmax ↑ 30%
(inhibition of CYP3A enzymes)
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Fluconazole Not studied. Concomitant use of No dose adjustment is required.
Itraconazole REKAMBYS with azole antifungal
Posaconazole agents may cause an increase in the
Voriconazole plasma concentrations of rilpivirine.

ANTIMYCOBACTERIALS
Rifabutin* rifabutin AUC ↔ REKAMBYS must not be used in
300 mg once daily† rifabutin Cmin ↔ combination with rifabutin as
rifabutin Cmax ↔ specific dosing recommendations
25-O-desacetyl-rifabutin AUC ↔ have not been established.
25-O-desacetyl-rifabutin Cmin ↔ Co-administration is likely to result
25-O-desacetyl-rifabutin Cmax ↔ in loss of therapeutic effect of
rilpivirine (see section 4.3).
300 mg once daily rilpivirine AUC ↓ 42%
(+ 25 mg once daily rilpivirine Cmin ↓ 48%
rilpivirine) rilpivirine Cmax ↓ 31%
300 mg once daily rilpivirine AUC ↑ 16%*

(+ 50 mg once daily rilpivirine Cmin ↔*
rilpivirine) rilpivirine Cmax ↑ 43%*
* compared to 25 mg once daily rilpivirine

alone
(induction of CYP3A enzymes)

Rifampicin*# rifampicin AUC ↔ Rilpivirine must not be used in
600 mg once daily rifampicin Cmin NA combination with rifampicin as
rifampicin Cmax ↔ co-administration is likely to result
25-desacetyl-rifampicin AUC ↓ 9% in loss of therapeutic effect of
25-desacetyl-rifampicin Cmin NA rilpivirine (see section 4.3).
25-desacetyl-rifampicin Cmax ↔
rilpivirine AUC ↓ 80%
rilpivirine Cmin ↓ 89%
rilpivirine Cmax ↓ 69%
(induction of CYP3A enzymes)

Rifapentine Not studied. Significant decreases in Rilpivirine must not be used in
rilpivirine plasma concentrations are combination with rifapentine as
expected. co-administration is likely to result
in loss of therapeutic effect of
(induction of CYP3A enzymes) rilpivirine (see section 4.3).
MACROLIDE ANTIBIOTICS
Clarithromycin Not studied. Increased exposure of Where possible, alternatives such as
Erythromycin rilpivirine is expected. azithromycin should be considered.

GLUCOCORTICOIDS OR CORTICOSTEROIDS
Dexamethasone Not studied. Dose dependent Rilpivirine should not be used in
(systemic, except for decreases in rilpivirine plasma combination with systemic
single dose use) concentrations are expected. dexamethasone (except as a single
dose) as co-administration may
(induction of CYP3A enzymes) result in loss of therapeutic effect of
rilpivirine (see section 4.3).
Alternatives should be considered,
particularly for long-term use.
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NARCOTIC ANALGESICS
Methadone* R(-) methadone AUC ↓ 16% No dose adjustments are required
60-100 mg once daily, R(-) methadone Cmin ↓ 22% when initiating co-administration of
individualised dose R(-) methadone Cmax ↓ 14% methadone with rilpivirine.
rilpivirine AUC ↔* However, clinical monitoring is
rilpivirine Cmin ↔* recommended as methadone
rilpivirine Cmax ↔* maintenance therapy may need to
* based on historic controls be adjusted in some patients.
ANTIARRHYTHMICS
Digoxin* digoxin AUC ↔ No dose adjustment is required.
digoxin Cmin NA
digoxin Cmax ↔
ANTIDIABETICS
Metformin* metformin AUC ↔ No dose adjustment is required.
metformin Cmin NA
metformin Cmax ↔
HERBAL PRODUCTS
St John's wort Not studied. Significant decreases in Rilpivirine must not be used in
(Hypericum perforatum) rilpivirine plasma concentrations are combination with products
expected. containing St John’s wort as
co-administration may result in loss
(induction of CYP3A enzymes) of therapeutic effect of rilpivirine
(see section 4.3).
ANALGESICS
Paracetamol*# paracetamol AUC ↔ No dose adjustment is required.
500 mg single dose paracetamol Cmin NA
paracetamol Cmax ↔
rilpivirine AUC ↔
rilpivirine Cmin ↑ 26%
ORAL CONTRACEPTIVES
Ethinylestradiol* ethinylestradiol AUC ↔ No dose adjustment is required.
0.035 mg once daily ethinylestradiol Cmin ↔
Norethindrone* ethinylestradiol Cmax ↑ 17%
1 mg once daily norethindrone AUC ↔
norethindrone Cmin ↔
norethindrone Cmax ↔
rilpivirine AUC ↔*
rilpivirine Cmin ↔*
rilpivirine Cmax ↔*
* based on historic controls
HMG CO-A REDUCTASE INHIBITORS
Atorvastatin*# atorvastatin AUC ↔ No dose adjustment is required.
40 mg once daily atorvastatin Cmin ↓ 15%
atorvastatin Cmax ↑ 35%
rilpivirine AUC ↔
rilpivirine Cmin ↔
rilpivirine Cmax ↓ 9%
PHOSPHODIESTERASE TYPE 5 (PDE-5) INHIBITORS
Sildenafil*# sildenafil AUC ↔ No dose adjustment is required.
50 mg single dose sildenafil Cmin NA
sildenafil Cmax ↔
rilpivirine AUC ↔
rilpivirine Cmin ↔
Vardenafil Not studied. No dose adjustment is required.
Tadalafil
10
Ω
% increase/decrease based on Drug-Drug Interaction studies with oral rilpivirine
* The interaction between rilpivirine and the medicinal product was evaluated in a clinical study. All other drug-drug
interactions shown are predicted.
#
This interaction study has been performed with a dose higher than the recommended dose for rilpivirine assessing the
maximal effect on the co-administered medicinal product. The dosing recommendation is applicable to the
recommended dose of rilpivirine of 25 mg once daily.
QT prolonging medicinal products

Oral rilpivirine at the recommended dose of 25 mg once daily is not associated with a clinically
relevant effect on QTc. Rilpivirine plasma concentrations after REKAMBYS injections at the
recommended dose of 600 mg monthly or 900 mg every 2 months, are comparable to those achieved
with oral rilpivirine at a dose of 25 mg qd. In a study of healthy subjects, supratherapeutic doses of
oral rilpivirine (75 mg once daily and 300 mg once daily) have been shown to prolong the QTc
interval of the ECG (see section 5.1). REKAMBYS should be used with caution when co-administered
with a medicinal product with a known risk of Torsade de Pointes (see section 4.4).
4.6 Fertility, pregnancy and lactation
Pregnancy
The effect of REKAMBYS on human pregnancy is unknown.
A moderate amount of data with oral rilpivirine in pregnant women (between 300-1000 pregnancy
outcomes) indicate no malformative or foetal/neonatal toxicity of rilpivirine.
A study of 19 pregnant women treated with oral rilpivirine in combination with a background regimen
during the second and third trimesters, and postpartum, showed lower exposures of oral rilpivirine
during pregnancy, therefore viral load should be monitored closely if REKAMBYS is used during
pregnancy.
Animal studies do not indicate reproductive toxicity (see section 5.3).
REKAMBYS is not recommended during pregnancy unless the expected benefit justifies the potential
risk.
An alternative oral regimen should be considered in line with current treatment guidelines. After
discontinuation of REKAMBYS, rilpivirine may remain in systemic circulation for up to 4 years in
some patients (see section 4.4).
Breast-feeding
It is expected that rilpivirine will be secreted into human milk based on animal data, although this has
not been confirmed in humans. Rilpivirine may be present in human milk for up to 4 years in some
patients after discontinuation of REKAMBYS.
It is recommended that HIV infected women do not breast-feed their infants under any circumstances
in order to avoid transmission of HIV.
Fertility
No human data on the effect of rilpivirine on fertility are available. No clinically relevant effects on
fertility were seen in animal studies (see section 5.3).
4.7 Effects on ability to drive and use machines
Patients should be informed that fatigue, dizziness and somnolence could occur when treated with
REKAMBYS (see section 4.8).
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4.8 Undesirable effects
Summary of the safety profile
The most frequently reported ARs from every 1 month dosing studies were injection site reactions (up
to 84%), headache (up to 12%) and pyrexia (10%).
The most frequently reported ARs from every 2 months dosing were injection site reactions (76%),
headache (7%) and pyrexia (7%).
Tabulated summary of adverse reactions

The ARs identified for rilpivirine and/or cabotegravir are listed by system organ class (SOC) and
frequency (see Table 6). Frequencies are defined as very common (≥ 1/10), common (≥ 1/100 to
< 1/10) and uncommon (≥ 1/1,000 to < 1/100).
Table 6: Tabulated summary of adverse reactions1

MedDRA System Organ Frequency ARs for rilpivirine + cabotegravir regimen
Class (SOC) Category
Blood and lymphatic Common decreased white blood cell count2, decreased
system disorders haemoglobin2, decreased platelet count2
Immune System Disorders Uncommon immune reactivation syndrome2
Metabolism and nutrition Very common increased total cholesterol (fasted)2, increased LDL
disorders cholesterol (fasted)2
Common decreased appetite2, increased triglycerides (fasted)2
Psychiatric disorders Common depression, anxiety, abnormal dreams, insomnia,
sleep disorder2, depressed mood2
Nervous system disorders Very common headache
Common dizziness
Uncommon somnolence, vasovagal reactions (in response to
injections)
Gastrointestinal disorders Very common increased pancreatic amylase2
Common nausea, vomiting, abdominal pain3, flatulence,
diarrhoea, abdominal discomfort2, dry mouth2,
increased lipase2
Hepatobiliary disorders Uncommon hepatotoxicity

Skin and subcutaneous Common rash4
tissue disorders
Musculoskeletal and Common myalgia
connective tissue disorders
General disorders and Very common injection site reactions (pain and discomfort, nodule,
administrative site induration), pyrexia5
conditions Common injection site reactions (swelling, erythema, pruritis,
bruising, warmth, haematoma), fatigue, asthenia,
malaise
Uncommon injection site reactions (cellulitis, abscess,
anaesthesia, haemorrhage, discolouration)
Investigations Common weight increased
Uncommon transaminase increased, blood bilirubin increased
1
The frequency of the identified ARs are based on all reported occurrences of the events and are not limited to those
considered at least possibly related by the investigator.
2
Additional adverse reactions seen with oral rilpivirine in other studies.
3
Abdominal pain includes the following grouped MedDRA preferred term: abdominal pain, upper abdominal pain.
4
Rash includes the following grouped MedDRA preferred terms: rash, rash erythematous, rash generalised, rash
macular, rash maculo-papular, rash morbilliform, rash papular, rash pruritic.
5
Pyrexia includes the following grouped MedDRA preferred terms: pyrexia, feeling hot, body temperature increased.
12
Description of selected adverse reactions
Local Injection Site Reactions (ISRs)

Up to 1% of subjects discontinued treatment with rilpivirine and cabotegravir injections because of
ISRs.
Injection site reactions were generally mild (Grade 1, 70%-75% of subjects) or moderate (Grade 2,
27%-36% of subjects). 3-4% of subjects experienced severe (Grade 3) ISRs. The median duration of
ISR events was 3 days. The percentage of subjects reporting ISRs decreased over time.
Weight increased
At the Week 48 time point, subjects in Phase 3 Studies FLAIR and ATLAS, who received rilpivirine
plus cabotegravir gained a median of 1.5 kg in weight; subjects continuing on their current
antiretroviral regimen (CAR) group gained a median of 1.0 kg (pooled analysis).
In the individual studies FLAIR and ATLAS, the median weight gains in the rilpivirine plus
cabotegravir arms were 1.3 kg and 1.8 kg respectively, compared to 1.5 kg and 0.3 kg in the CAR
arms.
At the 48 week timepoint, in ATLAS-2M the median weight gain in both the monthly and every
2 months rilpivirine+cabotegravir dosing arms was 1.0 kg.
Changes in laboratory chemistry

Elevated transaminases (ALT/AST) were observed in subjects receiving rilpivirine plus cabotegravir
during the clinical studies. These elevations were primarily attributed to acute viral hepatitis. A few
subjects on oral rilpivirine plus oral cabotegravir treatment had transaminase elevations attributed to
suspected drug-related hepatotoxicity; these changes were reversible upon discontinuation of
treatment.
Small, non-progressive increases in total bilirubin (without clinical jaundice) were observed with
treatment with rilpivirine plus cabotegravir. These changes are not considered clinically relevant as
they likely reflect competition between cabotegravir and unconjugated bilirubin for a common
clearance pathway (UGT1A1).
Elevated lipases were observed during clinical trials with rilpivirine plus cabotegravir. Grade 3 and 4
lipase increases occurred at a higher incidence with rilpivirine plus cabotegravir compared with CAR.
These elevations were generally asymptomatic and did not lead to rilpivirine plus cabotegravir
discontinuation. One case of fatal pancreatitis with Grade 4 lipase and confounding factors (including
history of pancreatitis) has been reported in study ATLAS-2M for which the causality to the injection
regimen could not be ruled out.
Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It
allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare
professionals are asked to report any suspected adverse reactions via the national reporting system
listed in Appendix V.
4.9 Overdose
There is currently limited experience with REKAMBYS overdose. If overdose occurs, the patient
should be treated supportively and as clinically indicated, with monitoring of vital signs and ECG (QT
interval), as necessary. Since rilpivirine is highly bound to plasma protein, dialysis is unlikely to result
in significant removal of the active substance.
13
5. PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
Pharmacotherapeutic group: Antiviral for systemic use, non-nucleoside reverse transcriptase

inhibitors, ATC code: J05AG05
Mechanism of action
Rilpivirine is a diarylpyrimidine non-nucleoside reverse-transcriptase inhibitor (NNRTI) of HIV-1.

Rilpivirine activity is mediated by non-competitive inhibition of HIV-1 reverse transcriptase (RT).
Rilpivirine does not inhibit the human cellular DNA polymerases α, β and γ.
Antiviral activity in vitro
Rilpivirine exhibited activity against laboratory strains of wild-type HIV-1 in an acutely infected
T-cell line with a median EC50 value for HIV-1/IIIB of 0.73 nM (0.27 ng/mL). Although rilpivirine
demonstrated limited in vitro activity against HIV-2 with EC50 values ranging from 2,510 to
10,830 nM (920 to 3,970 ng/mL), treatment of HIV-2 infection with rilpivirine is not recommended in
the absence of clinical data.
Rilpivirine also demonstrated antiviral activity against a broad panel of HIV-1 group M (subtype A, B,
C, D, F, G, H) primary isolates with EC50 values ranging from 0.07 to 1.01 nM (0.03 to 0.37 ng/mL)
and group O primary isolates with EC50 values ranging from 2.88 to 8.45 nM (1.06 to 3.10 ng/mL).
Resistance
Considering all of the available in vitro data and in vivo data generated with oral rilpivirine in
previously untreated patients, the following resistance-associated mutations, when present at baseline,
may affect the activity of rilpivirine: K101E, K101P, E138A, E138G, E138K, E138R, E138Q, V179L,
Y181C, Y181I, Y181V, Y188L, H221Y, F227C, M230I, M230L, and the combination of L100I and
K103N.
In cell culture
Rilpivirine-resistant strains were selected in cell culture starting from wild-type HIV-1 of different
origins and subtypes as well as NNRTI resistant HIV-1. The most commonly observed
resistance-associated mutations that emerged included L100I, K101E, V108I, E138K, V179F, Y181C,
H221Y, F227C and M230I.
Virologically suppressed patients:

The number of subjects who met confirmed virologic failure (CVF) criteria was low across the pooled
Phase 3 studies ATLAS and FLAIR. There were 7 CVFs on rilpivirine plus cabotegravir (7/591, 1.2%)
and 7 CVFs on current antiretroviral regimen (7/591, 1.2%) through week 48. In the rilpivirine plus
cabotegravir group in the pooled analysis, 5/591 (0.8%) subjects had resistance development: 5/591
(0.8%) and 4/591 (0.7%) with resistance-associated mutations to rilpivirine (K101E [n=1],
E138A/E/K/T [n=1], E138A [n=1], or E138K [n=2]) and/or cabotegravir (G140R [n=1], Q148R
[n=2], or N155H [n=1]), respectively. The 4 CVFs on cabotegravir plus rilpivirine in FLAIR had
HIV-1 subtype A1 (n=3) or AG (n=1). One CVF in FLAIR never received an injection. The 3 CVFs
on cabotegravir plus rilpivirine in ATLAS had HIV-1 subtype A, A1, or AG. In 2 of these 3 CVFs the
rilpivirine resistance-associated mutations observed at failure were also observed at baseline in PBMC
HIV-1 DNA.
In the ATLAS-2M study 10 subjects met CVF criteria through week 48: 8/522 (1.5%) in the Q8W arm
and 2/523 (0.4%) in the Q4W arm. In the Q8W group 5/522 (1.0%) had resistance development: 4/522
(0.8%) and 5/522 (1.0%) with resistance-associated mutations to rilpivirine (E138A [n=1], E138K
[n=1], K101E [n=2], or Y188L [n=1]) and/or cabotegravir (Q148R [n=3] or N155H [n=4]),
respectively. In the Q4W group 2/523 (0.4%) had resistance development: 1/523 (0.2%) and 2/523
(0.4%) had rilpivirine (K101E [n=1], M230L [n=1]) and/or cabotegravir (E138K [n=1], Q148R [n=1],
14
or N155H [n=1]) resistance-associated mutations, respectively. At baseline in the Q8W arm, 5 subjects
had rilpivirine resistance-associated mutations and 1 of those subjects carried a cabotegravir
resistance-associated mutation. Neither subject in the Q4W arm had any rilpivirine or cabotegravir
resistance-assocaiated mutation at baseline. The 10 CVFs on cabotegravir plus rilpivirine in ATLAS-
2M had HIV-1 subtype A (n=1), A1 (n=2), B (n=4), C (n=2), or Complex (n=1).
Cross-resistance
Site-directed NNRTI mutant virus

In a panel of 67 HIV-1 recombinant laboratory strains with one mutation at RT positions associated
with NNRTI resistance, including the most commonly found K103N and Y181C, rilpivirine showed
antiviral activity against 64 (96%) of these strains. The single resistance-associated mutations
associated with a loss of susceptibility to rilpivirine were: K101P, Y181I and Y181V. The K103N
mutation did not result in reduced susceptibility to rilpivirine by itself, but the combination of K103N
and L100I resulted in a 7-fold reduced susceptibility to rilpivirine.
Recombinant clinical isolates

Rilpivirine retained sensitivity (fold change ≤ biological cut-off) against 62% of 4,786 HIV-1
recombinant clinical isolates resistant to efavirenz and/or nevirapine.
Virologically suppressed patients

In the week 48 analysis of the Phase 3 studies ATLAS and FLAIR, 5/7 CVFs had phenotypic
resistance against rilpivirine at failure. Among these 5 patients, phenotypic cross-resistance was
observed against efavirenz (n=4), etravirine (n=3), and nevirapine (n=4).
Effects on electrocardiogram
No effect on QTcF interval was shown for oral rilpivirine at the recommended dose of 25 mg once
daily in a randomised, placebo and active (moxifloxacin 400 mg once daily) controlled crossover
study in 60 healthy adults, with 13 measurements over 24 hours at steady-state. Plasma rilpivirine
concentrations after REKAMBYS injections are comparable to those achieved with oral rilpivirine at
dose of 25 mg qd. REKAMBYS at the recommended dose of 600 mg monthly or 900 mg every
2 months is not associated with a clinically relevant effect on QTc.
When supratherapeutic doses of 75 mg once daily and 300 mg once daily of oral rilpivirine were
studied in healthy adults, the maximum mean time-matched (95% upper confidence bound)
differences in QTcF interval from placebo after baseline correction were 10.7 (15.3) and 23.3 (28.4)
ms, respectively. Steady-state administration of oral rilpivirine 75 mg once daily and 300 mg once
daily resulted in a mean Cmax approximately 4.4-fold and 11.6-fold, respectively, higher than the mean
steady-state Cmax observed with the recommended 600 mg once monthly dose of REKAMBYS. Steady
state administration of oral rilpivirine 75 mg once daily and 300 mg once daily resulted in a mean Cmax
approximately 4.1-fold and 10.7-fold, respectively, higher than the mean steady state Cmax observed
with the recommended 900 mg every 2 months dose of REKAMBYS.
Clinical efficacy and safety
Every 1 month dosing
The efficacy of REKAMBYS plus cabotegravir injection has been evaluated in two Phase 3
randomised, multicentre, active-controlled, parallel-arm, open-label, non-inferiority studies, FLAIR
(201584) and ATLAS (201585). The primary analysis was conducted after all subjects completed their
week 48 visit or discontinued the study prematurely.
Patients virologically suppressed (on prior dolutegravir-based regimen for 20 weeks)

In FLAIR, 629 HIV-1-infected, antiretroviral treatment (ART)-naive subjects received a dolutegravir
integrase strand transfer inhibitor (INI) containing regimen for 20 weeks (either
dolutegravir/abacavir/lamivudine or dolutegravir + 2 other nucleoside reverse transcriptase inhibitors
15
if subjects were HLA-B*5701 positive). Subjects who were virologically suppressed (HIV-1 RNA
< 50 copies per mL, n=566) were then randomised (1:1) to receive either a rilpivirine plus
cabotegravir regimen or remain on the CAR. Subjects randomised to receive the rilpivirine plus
cabotegravir regimen, initiated treatment with oral lead-in dosing with a cabotegravir (30 mg) tablet
plus a rilpivirine (25 mg) tablet once daily for at least 4 weeks, followed by treatment with
cabotegravir injection (month 1: 600 mg, month 2 onwards: 400 mg injection) plus rilpivirine injection
(month 1: 900 mg injection, month 2 onwards: 600 mg injection), monthly, for up to 96 weeks.
Patients virologically suppressed (stable on prior ART for at least 6 months)

In ATLAS, 616 HIV-1-infected, ART-experienced, virologically-suppressed (for at least 6 months)
subjects (HIV-1 RNA < 50 copies per mL) were randomised (1:1) and received either a rilpivirine plus
cabotegravir regimen or remained on the CAR. Subjects randomised to receive the rilpivirine plus
cabotegravir regimen initiated treatment with oral lead-in dosing with a cabotegravir (30 mg) tablet
plus a rilpivirine (25 mg) tablet once daily for at least 4 weeks, followed by treatment with
cabotegravir injection (month 1: 600 mg, month 2 onwards: 400 mg injection) plus rilpivirine injection
(month 1: 900 mg injection, month 2 onwards: 600 mg injection), monthly, for an additional 44 weeks.
In ATLAS, 50%, 17%, and 33% of subjects received an NNRTI, PI, or INI (respectively) as their
baseline third treatment agent class prior to randomisation and this was similar between treatment
arms.
Pooled Phase 3 studies

At baseline, in the pooled analysis, in the rilpivirine plus cabotegravir arm the median age of subjects
was 38 years, 27% were female, 27% were non-white, 1% were ≥ 65 years and 7% had CD4+ cell
count less than 350 cells per mm3; these characteristics were similar between treatment arms.
The primary endpoint of both studies was the proportion of subjects with plasma HIV-1 RNA
≥ 50 copies/mL at week 48 (snapshot algorithm for the ITT-E population).
In a pooled analysis of the two Phase 3 studies, rilpivirine plus cabotegravir was non-inferior to CAR
on the proportion of subjects having plasma HIV-1 RNA ≥ 50 c/mL (1.9% and 1.7% respectively) at
week 48. The adjusted treatment difference between rilpivirine plus cabotegravir and CAR (0.2; 95%
CI: -1.4, 1.7) met the non-inferiority criterion (upper bound of the 95% CI below 4%) [See Table 7].
The primary endpoint and other week 48 outcomes, including outcomes by key baseline factors, for
FLAIR, ATLAS, and pooled data are shown in Table 7 and Table 8.
Table 7: Virologic outcomes of randomised treatment in FLAIR and ATLAS at week 48

(Snapshot analysis)
FLAIR ATLAS Pooled Data
RPV+ RPV+
CAB CAR CAB CAR RPV+ CAB CAR
N=283 N=283 N=308 N=308 N=591 N=591
HIV-1
6 (2.1) 7 (2.5) 5 (1.6) 3 (1.0) 11 (1.9) 10 (1.7)
RNA ≥ 50 copies/mL†
Treatment
Difference % (95% -0.4 (-2.8, 2.1) 0.7 (-1.2, 2.5) 0.2 (-1.4, 1.7)
CI)*
HIV-1 RNA 265 (93.6) 264 (93.3) 285 (92.5) 294 (95.5) 550 (93.1) 558 (94.4)
< 50 copies/mL
Treatment Difference 0.4 (-3.7, 4.5) -3.0 (-6.7, 0.7) -1.4 (-4.1, 1.4)
% (95% CI)*
No virologic data at
12 (4.2) 12 (4.2) 18 (5.8) 11 (3.6) 30 (5.1) 23 (3.9)
week 48 window
Reasons
Discontinued
study/study drug
8 (2.8) 2 (0.7) 11 (3.6) 5 (1.6) 19 (3.2) 7 (1.2)
due to adverse
event or death
16
Discontinued
study/study drug 4 (1.4) 10 (3.5) 7 (2.3) 6 (1.9) 11 (1.9) 16 (2.7)
for other reasons
Missing data
during window but 0 0 0 0 0 0
on study
* Adjusted for baseline stratification factors.
†
Includes subjects who discontinued for lack of efficacy, discontinued while not suppressed.
N=Number of subjects in each treatment group, CI=confidence interval, CAR=current antiretroviral regimen,
RPV=rilpivirine, CAB=cabotegravir.
Table 8 Proportion of subjects with plasma HIV-1 RNA ≥ 50 copies/mL at week 48 for key
baseline factors (Snapshot outcomes)
Pooled data from FLAIR and ATLAS
RPV+CAB CAR
Baseline factors
N=591 N=591
n/N (%) n/N (%)
Baseline CD4+ < 350 0/42 2/54 (3.7)
(cells/ mm3) ≥ 350 to < 500 5/120 (4.2) 0/117
≥ 500 6/429 (1.4) 8/420 (1.9)
Gender Male 6/429 (1.4) 9/423 (2.1)
Female 5/162 (3.1) 1/168 (0.6)
Race White 9/430 (2.1) 7/408 (1.7)
Black African/American 2/109 (1.8) 3/133 (2.3)
Asian/Other 0/52 0/48
2
BMI < 30 kg/m 6/491 (1.2) 8/488 (1.6)
≥ 30 kg/m2 5/100 (5.0) 2/103 (1.9)
Age (years) < 50 9/492 (1.8) 8/466 (1.7)
≥ 50 2/99 (2.0) 2/125 (1.6)
Baseline antiviral PI 1/51 (2.0) 0/54
therapy at randomisation INI 6/385 (1.6) 9/382 (2.4)
NNRTI 4/155 (2.6) 1/155 (0.6)
BMI=body mass index, PI=Protease inhibitor, INI=Integrase inhibitor, NNRTI=non-nucleoside reverse
transcriptase inhibitor, RPV=rilpivirine, CAB=cabotegravir, CAR=current antiretroviral regimen
In the FLAIR and ATLAS studies, treatment differences across baseline characteristics (CD4+ count,
gender, age, race, BMI, baseline third agent treatment class) were comparable.
In the FLAIR study at 96 Weeks, the results remained consistent with the results at 48 Weeks. The
proportion of subjects having plasma HIV-1 RNA ≥ 50 c/mL in rilpivirine plus cabotegravir (n=283)
and CAR (n=283) was 3.2% and 3.2% respectively (adjusted treatment difference between
REKAMBYS plus cabotegravir and CAR [0.0; 95% CI: -2.9, 2.9]). The proportion of subjects having
plasma HIV-1 RNA < 50 c/mL in REKAMBYS plus cabotegravir and CAR was 87% and 89%,
respectively (adjusted treatment difference between REKAMBYS plus cabotegravir and CAR [-2.8;
95% CI: -8.2, 2.5]).
Every 2 months dosing
Patients virologically suppressed (stable on prior ART for at least 6 months)

The efficacy and safety of rilpivirine injection given every 2 months, has been evaluated in one
Phase 3b randomised, multicentre, parallel-arm, open-label, non-inferiority study, ATLAS-2M
(207966). The primary analysis was conducted after all subjects completed their week 48 visit or
discontinued the study prematurely.
In ATLAS-2M, 1045 HIV-1 infected, ART-experienced, virologically suppressed subjects were

randomised (1:1) and received a rilpivirine plus cabotegravir injection regimen administered either
every 2 months or monthly. Subjects initially on non-cabotegravir/rilpivirine treatment received oral
lead-in treatment comprising one rilpivirine tablet (25 mg) plus one cabotegravir tablet (30 mg), daily,
17
for at least 4 weeks. Subjects randomised to monthly rilpivirine injections (month 1: 900 mg injection,
month 2 onwards: 600 mg injection) and cabotegravir injections (month 1: 600 mg injection, month 2
onwards: 400 mg injection administered) received treatment for an additional 44 weeks. Subjects
randomised to every 2 months rilpivirine injections (900 mg injection at months 1, 2, 4 and every
2 months thereafter) and cabotegravir injections (600 mg injection at months 1, 2, 4 and every
2 months thereafter) received treatment for an additional 44 weeks. Prior to randomisation, 63%, 13%
and 24% of subjects received rilpivirine plus cabotegravir for 0 weeks, 1 to 24 weeks and > 24 weeks,
respectively.
At baseline, the median age of subjects was 42 years, 27% were female, 27% were non-white, 4%
were ≥65 years, and 6% had a CD4+ cell count less than 350 cells per mm3; these characteristics were
similar between the treatment arms.
The primary endpoint in ATLAS-2M was the proportion of subjects with a plasma HIV-1 RNA
≥50 c/mL at week 48 (snapshot algorithm for the ITT-E population).
In ATLAS-2M, rilpivirine plus cabotegravir administered every 2 months was non-inferior to

cabotegravir and rilpivirine administered every month on the proportion of subjects having plasma
HIV-1 RNA ≥ 50 c/mL (1.7% and 1.0% respectively) at week 48. The adjusted treatment difference
between cabotegravir plus rilpivirine administered every 2 months and every month (0.8; 95% CI: -
0.6, 2.2) met the non-inferiority criterion (upper bound of the 95% CI below 4%).
Table 9 Virologic outcomes of randomised treatment of ATLAS-2M at 48 weeks

(Snapshot analysis)
Every 2 months Dosing Monthly Dosing (Q4W)
(Q8W)
N=522 (%) N=523 (%)
HIV-1 RNA≥ 50 copies/mL† 9 (1.7) 5 (1.0)
Treatment Difference % (95%
0.8 (-0.6, 2.2)
CI)*
HIV-1 RNA < 50 copies/mL 492 (94.3) 489 (93.5)
Treatment Difference % (95%
0.8 (-2.1, 3.7)
CI)*
No virologic data at week 48 21 (4.0) 29 (5.5)
window
Reasons:
Discontinued study due to AE 9 (1.7) 13 (2.5)
or death
Discontinued study for other 12 (2.3) 16 (3.1)
reasons
On study but missing data in 0 0
window
* Adjusted for baseline stratification factors.
† Includes subjects who discontinued for lack of efficacy, discontinued while not suppressed.
N=Number of subjects in each treatment group, CI=confidence interval, CAR=current antiretroviral regimen.
Table 10 Proportion of subjects with plasma HIV-1 RNA ≥ 50 copies/mL in ATLAS-2M at

week 48 for key baseline factors (Snapshot outcomes).
Number of HIV-1 RNA ≥ 50 c/mL/ Total Assessed (%)
Baseline factors Every 2 months dosing
Monthly dosing (Q4W)
(Q8W)
Baseline CD4+ cell < 350 1/ 35 (2.9) 1/ 27 (3.7)
count (cells/mm3) 350 to < 500 1/ 96 (1.0) 0/ 89
≥ 500 7/391 (1.8) 4/407 (1.0)
Gender Male 4/385 (1.0) 5/380 (1.3)
Female 5/137 (3.5) 0/143
Race White 5/370 (1.4) 5/393 (1.3)
18
Non-White 4/152 (2.6) 0/130
Black/African
4/101 (4.0) 0/ 90
American
Non-
Black/African 5/421 (1.2) 5/421 (1.2)
American
BMI < 30 kg/m2 3/409 (0.7) 3/425 (0.7)
≥ 30 kg/m2 6/113 (5.3) 2/98 (2.0)
Age (years) < 35 4/137 (2.9) 1/145 (0.7)
35 to < 50 3/242 (1.2) 2/239 (0.8)
≥ 50 2/143 (1.4) 2/139 (1.4)
Prior exposure None 5/327 (1.5) 5/327 (1.5)
CAB/RPV 1-24 weeks 3/69 (4.3) 0/68
> 24 weeks 1/126 (0.8) 0/128
BMI=body mass index, CAB=cabotegravir, RPV=rilpivirine
In the ATLAS-2M study, treatment differences on the primary endpoint across baseline characteristics
(CD4+ lymphocyte count, gender, race, BMI, age and prior exposure to cabotegravir/rilpivirine) were
not clinically meaningful.
Post-hoc analysis
Multivariable analyses of pooled phase 3 studies (ATLAS, FLAIR, ATLAS-2M), including data from
1039 HIV-infected adults with no prior exposure to rilpivirine plus cabotegravir, examined the
influence of the following covariates: baseline viral and participants characteristics, dosing regimen
(Q4W or Q8W), and post-baseline plasma drug concentrations on CVF using regression modeling
with a covariate selection procedure. Through Week 48 in these studies, 13/1039 (1.25%) participants
had CVF while receiving rilpivirine plus cabotegravir.
Four covariates were significantly associated (P < 0.05 for each adjusted odds ratio) with increased
risk of CVF: rilpivirine resistance associated mutations (RAMs) at baseline identified by proviral
DNA genotypic assay, HIV-1 subtype A6/A1 (associated with integrase L74I polymorphism),
rilpivirine trough concentration 4 weeks following initial injection dose, BMI of at least 30 kg/m2
(associated with cabotegravir pharmacokinetics). Other covariates including Q4W or Q8W dosing,
female gender, or other viral subtypes (non A6/A1) had no significant association with CVF. No
baseline factor, when present in isolation, was predictive of virologic failure. However, a combination
of at least 2 of the following baseline factors was associated with increased risk of CVF: rilpivirine
resistance associated mutations, HIV-1 subtype A6/A1, or BMI ≥ 30 kg/m2 (Table 11).
Table 11 Week 48 Outcomes by Presence of Key Baseline Factors of rilpivirine resistance

associated mutations, HIV-1 Subtype A6/A11 and BMI ≥ 30 kg/m2
Confirmed Virologic
Baseline Factors (number) Virologic Successes2
Failure (%)3
0 694/732 (94.8) 3/732 (0.41)
1 261/272 (96.0) 1/272 (0.37)4
≥2 25/35 (71.4) 9/35 (25.7)5
TOTAL 980/1039 (94.3) 13/1039 (1.25)
(95% Confidence Interval) (92.74%, 95.65%) (0.67%, 2.13%)
1
HIV-1 subtype A1 or A6 classification based on Los Alamos National Library panel from HIV Sequence database
(June 2020)
2
Based on the FDA Snapshot algorithm of RNA <50 copies/mL.
3
Defined as two consecutive measurements of HIV RNA >200 copies/mL.
4
Positive Predictive Value (PPV) <1%; Negative Predictive Value (NPV) 98%; sensitivity 8%; specificity 74%
5
PPV 26%; NPV 99.6%; sensitivity 69%; specificity 97.5%
19
Paediatric population
The European Medicines Agency has deferred the obligation to submit the results of studies with
REKAMBYS injection in one or more subsets of the paediatric population in the treatment of HIV-1
infection.
5.2 Pharmacokinetic properties
The pharmacokinetic properties of REKAMBYS have been evaluated in healthy and HIV-1 infected
adults.
Table 12: Population pharmacokinetic parameters following once-daily oral rilpivirine and
following initiation and monthly or every two months continuation intramuscular
injections of REKAMBYS
Geometric mean (5th; 95th Percentile)
Dosing phase Dose regimen AUC(0-tau)b Cmax Ctaub
(ng•h/mL) (ng/mL) (ng/mL)
25 mg 2,083 116 79.4
Oral Lead-Inc
once daily (1,125; 3,748) (48.6; 244) (31.8; 177)
a,d 900 mg IM 44,854 144 42.0
Initial Injection
initial dose (21,712; 87,528) (93.9; 220) (21.8; 78.9)
Monthly 600 mg IM 67,703 120 84.9
Injectiona,e monthly (39,029; 117,472) (68.2; 208) (49.4; 146)
Every 2 months 900 mg IM 127,031 133 65.6
Injectiona,e every 2 months (74,845; 211,644) (77.8; 223) (36.9; 113)
a
Based on individual post-hoc estimates from rilpivirine IM population pharmacokinetic model (pooled data FLAIR,
ATLAS and ATLAS-2M).
b
tau is dosing interval: 24 hours for oral; 1 or 2 months for monthly or every 2 months IM injections.
c
For oral rilpivirine, Ctau represents observed pooled data FLAIR, ATLAS and ATLAS-2M, AUC(0-tau) and Cmax
represent pharmacokinetic data from oral rilpivirine Phase 3 studies
d
Initial injection Cmax primarily reflects oral dosing because the initial injection was administered on the same day as
the last oral dose.
e
Week 48 data.
Absorption
Rilpivirine prolonged-release injection exhibits absorption rate-limited kinetics (ie, flip-flop

pharmacokinetics) resulting from slow absorption from the gluteal muscle into the systemic circulation
resulting in sustained rilpivirine plasma concentrations.
Following a single intramuscular dose, rilpivirine plasma concentrations are detectable the first day
and gradually rise to reach maximum plasma concentrations after a median of 3-4 days. Rilpivirine has
been detected in plasma up to 52 weeks or longer after administration of a single dose of
REKAMBYS. After 1 year of monthly or every 2 months injections, approximately 80% of the
rilpivirine pharmacokinetic steady-state exposure is reached.
Plasma rilpivirine exposure increases in proportion or slightly less than in proportion to dose following
single and repeat IM injections of doses ranging from 300 to 1200 mg.
Distribution
Rilpivirine is approximately 99.7% bound to plasma proteins in vitro, primarily to albumin. Based on
population pharmacokinetics analysis, the typical apparent volume of the central compartment (Vc/F)
for rilpivirine after IM administration was estimated to be 132 L, reflecting a moderate distribution to
peripheral tissues.
20
Rilpivirine is present in cerebrospinal fluid (CSF). In HIV-1-infected subjects receiving a regimen of
rilpivirine injection plus cabotegravir injection, the median rilpivirine CSF to plasma concentration
ratio (n=16) was 1.07 to 1.32% (range: not quantifiable to 1.69%). Consistent with therapeutic
rilpivirine concentrations in the CSF, CSF HIV-1 RNA (n=16) was < 50 c/mL in 100% and < 2 c/mL
in 15/16 (94%) of subjects. At the same time point, plasma HIV-1 RNA (n=18) was < 50 c/mL in
100% and < 2 c/mL in 12/18 (66.7%) of subjects.
Biotransformation
In vitro experiments indicate that rilpivirine primarily undergoes oxidative metabolism mediated by
the cytochrome P450 (CYP) 3A system.
Elimination
The mean apparent half-life of rilpivirine following REKAMBYS administration is absorption

rate-limited and was estimated to be 13-28 weeks.
The apparent plasma clearance (CL/F) of rilpivirine was estimated to be 5.08 L/h.
After single dose administration of oral 14C-rilpivirine, on average 85% and 6.1% of the radioactivity
could be retrieved in faeces and urine, respectively. In faeces, unchanged rilpivirine accounted for on
average 25% of the administered dose. Only trace amounts of unchanged rilpivirine (< 1% of dose)
were detected in urine.
Special patient populations
Gender
No clinically relevant differences in the rilpivirine exposure after intramuscular (IM) administration
have been observed between men and women.
Race
No clinically relevant effect of race on the rilpivirine exposure after intramuscular administration has
been observed.
BMI
No clinically relevant effect of BMI on the rilpivirine exposure after intramuscular administration has
been observed.
Elderly
No clinically relevant effect of age on the rilpivirine exposure after intramuscular administration has
been observed. Pharmacokinetic data for rilpivirine in subjects of > 65 years old are limited.
Renal impairment
The pharmacokinetics of rilpivirine have not been studied in patients with renal insufficiency. Renal
elimination of rilpivirine is negligible. No dose adjustment is needed for patients with mild or
moderate renal impairment. In patients with severe renal impairment or end-stage renal disease,
REKAMBYS should be used with caution, as plasma concentrations may be increased due to
alteration of drug absorption, distribution and/or metabolism secondary to renal dysfunction. In
patients with severe renal impairment or end-stage renal disease, the combination of REKAMBYS
with a strong CYP3A inhibitor should only be used if the benefit outweighs the risk. As rilpivirine is
highly bound to plasma proteins, it is unlikely that it will be significantly removed by haemodialysis
or peritoneal dialysis (see section 4.2).
Hepatic impairment
Rilpivirine is primarily metabolised and eliminated by the liver. In a study comparing 8 patients with
mild hepatic impairment (Child-Pugh score A) to 8 matched controls, and 8 patients with moderate
hepatic impairment (Child-Pugh score B) to 8 matched controls, the multiple dose exposure of oral
21
rilpivirine was 47% higher in patients with mild hepatic impairment and 5% higher in patients with
moderate hepatic impairment. However, it may not be excluded that the pharmacologically active,
unbound, rilpivirine exposure is significantly increased in moderate hepatic impairment. No dose
adjustment is suggested but caution is advised in patients with moderate hepatic impairment.
REKAMBYS has not been studied in patients with severe hepatic impairment (Child-Pugh score C).
Therefore, REKAMBYS is not recommended in patients with severe hepatic impairment (see
section 4.2).
HBV/HCV Co-infected Patients

Population pharmacokinetic analysis indicated that hepatitis B and/or C virus co-infection had no
clinically relevant effect on the rilpivirine exposure after oral rilpivirine intake.
Paediatric Patients
The phamacokinetics of rilpivirine in children and adolescents aged < 18 years have not been
established with REKAMBYS.
5.3 Preclinical safety data
All studies were performed with rilpivirine for oral use except for the studies on local tolerance with
REKAMBYS injections.
Repeated dose toxicity
Liver toxicity associated with liver enzyme induction was observed in rodents. In dogs,
cholestasis-like effects were noted.
Reproductive toxicology studies
Studies in animals have shown no evidence of relevant embryonic or foetal toxicity or an effect on
reproductive function. There was no teratogenicity with oral rilpivirine in rats and rabbits. The
exposures at the embryo-foetal No Observed Adverse Effects Levels (NOAELs) in rats and rabbits
were respectively ≥ 12 times and ≥ 57 times the exposure in humans at the maximum recommended
human daily dose of 25 mg once daily in HIV-1 infected patients or 600 mg or 900 mg intramuscular
injection dose of rilpivirine long-acting injectable suspension.
Carcinogenesis and mutagenesis
Oral rilpivirine was evaluated for carcinogenic potential by oral gavage administration to mice and rats
up to 104 weeks. At the lowest tested doses in the carcinogenicity studies, the systemic exposures
(based on AUC) to rilpivirine were ≥ 17 times (mice) and ≥ 2 times (rats) the exposure in humans at
the maximum recommended human daily dose of 25 mg once daily in HIV-1 infected patients or
600 mg or 900 mg intramuscular injection dose of rilpivirine long-acting injectable suspension. In rats,
there were no drug-related neoplasms. In mice, rilpivirine was positive for hepatocellular neoplasms in
both males and females. The observed hepatocellular findings in mice may be rodent-specific.
Rilpivirine has tested negative in the absence and presence of a metabolic activation system in the
in vitro Ames reverse mutation assay and the in vitro clastogenicity mouse lymphoma assay.
Rilpivirine did not induce chromosomal damage in the in vivo micronucleus test in mice.
Local tolerance for REKAMBYS
After long-term repeated IM administration of REKAMBYS in dogs and minipigs, slight, short-lasting
(ie, 1-4 days in minipigs) erythema was observed, and white deposits were noted at the injection sites
at necropsy, accompanied by swelling and discoloration of draining lymph nodes. Microscopic
examination showed macrophage infiltration and eosinophilic deposits at the injection sites. A
macrophage infiltration response was also noted in the draining/regional lymph nodes. These findings
were considered to be a reaction to the deposited material rather than a manifestation of local irritation.
22
6. PHARMACEUTICAL PARTICULARS
6.1 List of excipients
poloxamer 338
citric acid monohydrate
glucose monohydrate
sodium dihydrogen phosphate monohydrate
sodium hydroxide (to adjust pH and ensure isotonicity)
water for injections
6.2 Incompatibilities
This medicinal product must not be mixed with other medicinal products or diluents.
6.3 Shelf life
2 years
Chemical and physical in-use stability has been demonstrated for 6 hours at 25C.
Once the suspension has been drawn into the syringe, the injection should be administered as soon as
possible, but may remain in the syringe for up to 2 hours. If 2 hours are exceeded, the medicine,
syringe, and needle must be discarded.
6.4 Special precautions for storage
Store in a refrigerator (2°C - 8°C).

Do not freeze.
Prior to administration, the vial should be brought to room temperature (not to exceed 25°C). The vial
may remain in the carton at room temperature for up to 6 hours. If not used after 6 hours, it must be
discarded (refer to section 6.3).
6.5 Nature and contents of container
Type I glass vial.
600 mg pack
Each pack contains one clear 4-mL glass vial, with a butyl elastomer stopper and an aluminium
overseal with a plastic flip-off button, 1 syringe (0.2 mL graduation), 1 vial adaptor and 1 needle for
injection (23 gauge, 1½ inch).
900 mg pack
Each pack contains one clear 4-mL glass vial, with a butyl elastomer stopper and an aluminium
overseal with a plastic flip-off button, 1 syringe (0.2 mL graduation), 1 vial adaptor and 1 needle for
injection (23 gauge, 1½ inch).
6.6 Special precautions for disposal and other handling
Any unused medicinal product or waste material should be disposed of in accordance with local
requirements.
23
Full instructions for use and handling of REKAMBYS are provided in the package leaflet (see
Instructions for Use).
7. MARKETING AUTHORISATION HOLDER
Janssen-Cilag International NV
Turnhoutseweg 30
B-2340 Beerse
Belgium
8. MARKETING AUTHORISATION NUMBER
600 mg: EU/1/20/1482/001

900 mg: EU/1/20/1482/002
9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
10. DATE OF REVISION OF THE TEXT
Detailed information on this medicinal product is available on the website of the European Medicines
Agency http://www.ema.europa.eu/
24
ANNEX II
A. MANUFACTURER(S) RESPONSIBLE FOR BATCH

RELEASE
B. CONDITIONS OR RESTRICTIONS REGARDING SUPPLY

AND USE
C. OTHER CONDITIONS AND REQUIREMENTS OF THE

MARKETING AUTHORISATION
D. CONDITIONS OR RESTRICTIONS WITH REGARD TO

THE SAFE AND EFFECTIVE USE OF THE MEDICINAL
PRODUCT
25
A. MANUFACTURER(S) RESPONSIBLE FOR BATCH RELEASE
Name and address of the manufacturer(s) responsible for batch release
Janssen Pharmaceutica NV
Turnhoutseweg 30
B-2340 Beerse
Belgium
B. CONDITIONS OR RESTRICTIONS REGARDING SUPPLY AND USE
Medicinal product subject to restricted medical prescription (see Annex I: Summary of Product
Characteristics, section 4.2).
C. OTHER CONDITIONS AND REQUIREMENTS OF THE MARKETING

AUTHORISATION
 Periodic safety update reports (PSURs)
The requirements for submission of PSURs for this medicinal product are set out in the list of Union
reference dates (EURD list) provided for under Article 107c(7) of Directive 2001/83/EC and any
subsequent updates published on the European medicines web-portal.
The marketing authorisation holder (MAH) shall submit the first PSUR for this product within
6 months following authorisation.
D. CONDITIONS OR RESTRICTIONS WITH REGARD TO THE SAFE AND

EFFECTIVE USE OF THE MEDICINAL PRODUCT
 Risk management plan (RMP)
The marketing authorisation holder (MAH) shall perform the required pharmacovigilance activities
and interventions detailed in the agreed RMP presented in Module 1.8.2 of the marketing authorisation
and any agreed subsequent updates of the RMP.
An updated RMP should be submitted:

 At the request of the European Medicines Agency;
 Whenever the risk management system is modified, especially as the result of new information
being received that may lead to a significant change to the benefit/risk profile or as the result of
an important (pharmacovigilance or risk minimisation) milestone being reached.
 Obligation to conduct post-authorisation measures
The MAH shall complete, within the stated timeframe, the below measures:
26
Description Due date
The MAH will conduct a prospective cohort study (COMBINE-2 study) to collect September
data from patients in order to assess clinical effectiveness, adherence, durability 2026
and discontinuations after initiating the cabotegravir and rilpivirine long acting
regimen. The study will also monitor for resistance and response to subsequent
antiretroviral regimens among patients who switched from cabotegravir and
rilpivirine long acting regimen to another regimen. The MAH will submit interim
study results annually and the final results of the study by September 2026.
The MAH will conduct a real-world five-year Drug Utilisation Study (DUS). This September
observational cohort study will aim to better understand the patient population 2026
receiving cabotegravir long acting injection and/or rilpivirine long acting injection
containing regimens in routine clinical practice. The study will assess usage
patterns, adherence, and post marketing clinical effectiveness of these regimens
and monitor for resistance among virologic failures for whom data on resistance
testing are available. The MAH will submit interim study results annually and the
final results of the DUS by September 2026.
27
ANNEX III
LABELLING AND PACKAGE LEAFLET
28
A. LABELLING
29
PARTICULARS TO APPEAR ON THE OUTER PACKAGING
OUTER CARTON – 600 mg

rilpivirine
2. STATEMENT OF ACTIVE SUBSTANCE(S)
Each vial contains 600 mg of rilpivirine
3. LIST OF EXCIPIENTS
Excipients: poloxamer 338, citric acid monohydrate, glucose monohydrate, sodium dihydrogen
phosphate monohydrate, sodium hydroxide to adjust pH and ensure isotonicity, water for injections
4. PHARMACEUTICAL FORM AND CONTENTS

Contents:
1 vial
1 vial adaptor
1 syringe
1 injection needle
2 mL
5. METHOD AND ROUTE OF ADMINISTRATION
Read the package leaflet before use.
Open here
6. SPECIAL WARNING THAT THE MEDICINAL PRODUCT MUST BE STORED OUT

OF THE SIGHT AND REACH OF CHILDREN
Keep out of the sight and reach of children.
7. OTHER SPECIAL WARNING(S), IF NECESSARY
8. EXPIRY DATE
EXP
30
9. SPECIAL STORAGE CONDITIONS
Store at 2°C - 8°C. Do not freeze.
10. SPECIAL PRECAUTIONS FOR DISPOSAL OF UNUSED MEDICINAL PRODUCTS

OR WASTE MATERIALS DERIVED FROM SUCH MEDICINAL PRODUCTS, IF
APPROPRIATE
11. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER
Turnhoutseweg 30
B-2340 Beerse
Belgium
12. MARKETING AUTHORISATION NUMBER(S)
EU/1/20/1482/001
13. BATCH NUMBER
Lot
14. GENERAL CLASSIFICATION FOR SUPPLY
15. INSTRUCTIONS ON USE
16. INFORMATION IN BRAILLE
17. UNIQUE IDENTIFIER – 2D BARCODE
2D barcode carrying the unique identifier included.
18. UNIQUE IDENTIFIER – HUMAN READABLE DATA
PC
SN
NN
31
PARTICULARS TO APPEAR ON THE BACKING CARD (IN CARTON) – 600 mg

rilpivirine
2 mL
Read the Instructions For Use before preparing REKAMBYS

8. EXPIRY DATE

APPROPRIATE
EU/1/20/1482/001
32
13. BATCH NUMBER
33
MINIMUM PARTICULARS TO APPEAR ON SMALL IMMEDIATE PACKAGING UNITS
VIAL – 600 mg
REKAMBYS 600 mg
rilpivirine
IM
3. EXPIRY DATE
EXP
4. BATCH NUMBER
Lot
5. CONTENTS BY WEIGHT, BY VOLUME, OR UNIT
2 mL
6. OTHER
34
PARTICULARS TO APPEAR ON THE OUTER PACKAGING
OUTER CARTON – 900 mg

rilpivirine
Each vial contains 900 mg of rilpivirine
Excipients: poloxamer 338, citric acid monohydrate, glucose monohydrate, sodium dihydrogen
phosphate monohydrate, sodium hydroxide to adjust pH and ensure isotonicity, water for injections

Contents:
1 vial
1 vial adaptor
1 syringe
1 injection needle
3 mL
Read the package leaflet before use.
Open here

Keep out of the sight and reach of children.
8. EXPIRY DATE
EXP
35
Store at 2°C - 8°C. Do not freeze.

APPROPRIATE
Turnhoutseweg 30
B-2340 Beerse
Belgium
EU/1/20/1482/002
13. BATCH NUMBER
Lot
2D barcode carrying the unique identifier included.
PC
SN
NN
36
PARTICULARS TO APPEAR ON THE BACKING CARD (IN CARTON) – 900 mg

rilpivirine
3 mL
Read the Instructions For Use before preparing REKAMBYS

8. EXPIRY DATE

APPROPRIATE
EU/1/20/1482/002
37
13. BATCH NUMBER
38
MINIMUM PARTICULARS TO APPEAR ON SMALL IMMEDIATE PACKAGING UNITS
VIAL – 900 mg
REKAMBYS 900 mg
rilpivirine
IM
3. EXPIRY DATE
EXP
4. BATCH NUMBER
Lot
5. CONTENTS BY WEIGHT, BY VOLUME, OR UNIT
3 mL
6. OTHER
39
B. PACKAGE LEAFLET
40
Package leaflet: Information for the user
rilpivirine
Read all of this leaflet carefully before you start taking this medicine because it contains
important information for you.
- Keep this leaflet. You may need to read it again.
- If you have any further questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not pass it on to others. It may harm them,
even if their signs of illness are the same as yours.
- If you get any side effects, talk to your doctor or pharmacist. This includes any possible side
effects not listed in this leaflet. See section 4.
What is in this leaflet

1. What is REKAMBYS and what it is used for
2. What you need to know before you use REKAMBYS
3. How REKAMBYS is given
4. Possible side effects
5. How to store REKAMBYS
6. Contents of the pack and other information
1. What REKAMBYS is and what it is used for
REKAMBYS contains the active ingredient rilpivirine. It is one of a group of medicines called
non-nucleoside reverse transcriptase inhibitors (NNRTIs) that are used for the treatment of human
immunodeficiency virus type 1 (HIV-1) infection.
REKAMBYS works together with other HIV medicines to block the ability of the virus to make more
copies of itself. REKAMBYS injections do not cure HIV infection but help reduce the amount of HIV
in your body and keeps it at a low level. This holds off damage to the immune system and the
development of infections and diseases associated with AIDS.
REKAMBYS is always given with another HIV medicine called cabotegravir injection. They are used
together in adults aged 18 years and older whose HIV-1 infection is already under control.
Do not use REKAMBYS if you are allergic to rilpivirine or any of the other ingredients of this
medicine (listed in section 6).
Do not use REKAMBYS if you are taking any of the following medicines as they may affect the
way REKAMBYS or the other medicine works:
- carbamazepine, oxcarbazepine, phenobarbital, phenytoin (medicines to treat epilepsy and
prevent seizures)
- rifabutin, rifampicin, rifapentine (medicines to treat some bacterial infections such as
tuberculosis)
- dexamethasone (a corticosteroid used in a variety of conditions such as inflammation and
allergic reactions) as a course of treatment by mouth or injection
- products that contain St John’s wort (Hypericum perforatum, a herbal remedy used for
depression).
If you are taking any of the above, ask your doctor about alternatives.
Warnings and precautions

Talk to your doctor or pharmacist before using REKAMBYS.
41
REKAMBYS is not a cure for HIV infection. It is part of a treatment to reduce the amount of virus in
the blood. You can still pass on HIV when using this medicine, although the risk is lowered by
effective antiretroviral therapy. Discuss with your doctor the precautions you need to take to avoid
infecting other people.
Tell your doctor about your situation

Check the following points and tell your doctor if any of them apply to you.
- You must attend all the planned visits for injections, do not miss any visits, it is very important
for the success of your treatment. If you cannot attend a planned visit, inform your doctor as
soon as possible.
- Tell your doctor if you have ever had problems with your liver, including hepatitis B or
hepatitis C, or problems with your kidneys. Your doctor may check how well your liver or
kidneys work to decide if you can use REKAMBYS. See ‘Uncommon side effects’ in section 4
of this leaflet for signs of liver damage.
- Tell your doctor immediately if you notice any symptoms of infections (for example, fever,
chills, sweats). In some patients with HIV, inflammation from previous infections may occur
soon after starting HIV treatment. It is believed that these symptoms are due to an improvement
in the body’s immune response, enabling the body to fight infections that were present
previously but caused no obvious symptoms.
- Also tell your doctor straight away if you notice any symptoms such as muscle weakness,
weakness beginning in the hands and feet and moving up towards the trunk of the body,
palpitations, tremor or hyperactivity. This is because autoimmune disorders (conditions in
which the immune system mistakenly attacks healthy body tissue) may also occur after you start
taking medicines for the treatment of your HIV infection. Autoimmune disorders may occur
many months after the start of treatment.
- Tell your doctor if you are taking any medicines that you have been told may cause a life-
threatening irregular heartbeat (torsade de pointes).
Reactions to Injections
Post-injection reaction symptoms have happened within minutes in some people after receiving their
rilpivirine injection. Most symptoms resolved within a few minutes after the injection. Symptoms of
post-injection reactions may include: difficulty breathing, stomach cramps, sweating, numbness of
your mouth, feeling anxious, feeling warm, feeling lightheaded or feeling like you are going to pass
out (faint), and blood pressure changes. Tell your healthcare professional if you experience these
symptoms after you receive your injections.
Regular appointments are important

It is important that you attend your planned appointments to receive REKAMBYS, to control your
HIV infection and to stop your illness from getting worse. Do not miss any visits, it is very important
for the success of your treatment. If you cannot attend a planned visit, inform your doctor as soon as
possible. Talk to your doctor if you are thinking about stopping treatment. If you are late receiving
your REKAMBYS injection, or if you stop receiving REKAMBYS, you will need to take other
medicines to treat HIV infection and to reduce the risk of the virus becoming resistant as the drug
levels in your body will be too low to treat the HIV infection.
Children
REKAMBYS is not for use in children and adolescents less than 18 years of age, because it has not
been studied in these patients.
Other medicines and REKAMBYS

Tell your healthcare provider if you are taking, have recently taken or might take any other medicines.
Some medicines may affect the levels of REKAMBYS in the blood if you are taking them while being
treated with REKAMBYS, or REKAMBYS may affect how well the other medicine works.
42
prevent seizures)
tuberculosis)
depression).
The effects of REKAMBYS or other medicines might change if you use REKAMBYS together
with any of the following medicines:
- clarithromycin, erythromycin (antibiotics)
- methadone (used to treat narcotic withdrawal and dependence)
Pregnancy and breast-feeding

Tell your doctor immediately if you are pregnant or if you plan to become pregnant. Your doctor will
consider the benefit and the risk to you and your baby of using REKAMBYS while you are pregnant.
If you are planning to have a baby, talk to your doctor in advance, as rilpivirine can remain in your
body for up to 4 years after the last injection of REKAMBYS.
Women who have HIV must not breast-feed because HIV may pass into breast milk and infect the
baby.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines

Some patients may feel tired, dizzy or drowsy during treatment with REKAMBYS. Do not drive or
operate machinery if you have any of these side effects.
Important information about some of the ingredients of REKAMBYS

This medicine contains less than 1 mmol sodium (23 mg) per 2 mL injection, that is to say essentially
‘sodium-free’.
A nurse or doctor will give you REKAMBYS as an injection in the muscle of your buttock
(intramuscular, or IM injection).
You will be given your injection either once every month or once every 2 months, together with
another injectable medicine called cabotegravir. Your doctor will explain how often the medicine will
be given.
Before you start treatment with REKAMBYS, your doctor will prescribe you daily treatment with
rilpivirine and cabotegravir tablets for one month. This is called the lead-in period - taking the tablets
before you receive REKAMBYS and cabotegravir injections will allow your doctor to test how well
these medicines suit you.
43
If you are going to be given REKAMBYS every month, your treatment will be as follows:
When
Medicine month 1 (at least 28 days) month 2 (after one month 3 onwards
month of tablets)
Rilpivirine 25-mg tablet once daily single injection of 600 mg by injection every
900 mg month
Cabotegravir 30-mg tablet once daily single injection of 400 mg by injection every
600 mg month
If you are going to be given REKAMBYS every 2 months, your treatment will be as follows:
When
month of tablets)
and month 3
Rilpivirine 25-mg tablet, once daily single injection of 900 mg by injection, every
900 mg 2 months
Cabotegravir 30-mg tablet, once daily single injection of 600 mg by injection, every
600 mg 2 months
If you miss a REKAMBYS injection

It is important that you keep your regular planned appointments to receive your injection. If you miss
an appointment, contact your doctor immediately to make a new appointment.
Talk to your doctor if you think you will not be able to receive your REKAMBYS injection at the
usual time. Your doctor may recommend you take tablets instead, until you are able to have a
REKAMBYS injection again.
If you are given too much REKAMBYS

A doctor or nurse will give this medicine to you, so it is unlikely that you will be given too much. If
you are worried, tell the doctor or nurse.
Don’t stop using REKAMBYS without advice from your doctor.

Use REKAMBYS for as long as your doctor recommends. Don’t stop unless your doctor advises you
to.
Low levels of rilpivirine (the active ingredient of REKAMBYS) can remain in your body for up to
4 years after stopping treatment. However, once you received your last REKAMBYS injection, the
low levels of rilpivirine that remain will not work well enough against the virus which then can
become resistant. To keep your HIV-1 infection under control and to stop the virus becoming resistant,
you must start a different HIV treatment by the time your next REKAMBYS injection was planned.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following is a list of side effects that have been reported when REKAMBYS is used with
cabotegravir injection.
Very common side effects (affects at least 1 in 10 people)

 headache
 injection site reactions - these are generally mild to moderate and became less frequent over
time. Symptoms may include:
o very common: pain and discomfort, a hardened mass or lump
44
o common: redness, itching, swelling, bruising, warmth or discoloration.
o uncommon: numbness, minor bleeding, an abscess (collection of pus) or cellulitis (heat,
swelling or redness).
 feeling hot/feverish (pyrexia)
Common side effects (affects less than 1 in 10 people)

 depression
 anxiety
 abnormal dreams
 sleeping difficulty (insomnia)
 dizziness
 feeling sick (nausea)
 vomiting
 belly pain (abdominal pain)
 wind (flatulence)
 diarrhoea
 rash
 muscle pain (myalgia)
 tiredness (fatigue)
 feeling weak (asthenia)
 generally feeling unwell (malaise)
 weight gain
Uncommon side effects (affects less than 1 in 100 people)

 feeling drowsy (somnolence)
 feeling lightheaded, during or after an injection. This may lead to fainting.
 liver damage (signs may include yellowing of the skin and the whites of the eyes loss of
appetite, itching, tenderness in the belly, light-coloured stools or unusually dark urine).
 changes in liver blood tests (increase in transaminases)
 an increase in bilirubin (a substance produced by the liver) in the blood.
Other side effects

 Severe abdominal pain caused by inflammation of the pancreas (pancreatitis).
The following side effects that can occur with rilpivirine tablets may also occur with REKAMBYS
injection:
Very Common side effects

 increase in cholesterol and/or pancreatic amylase in your blood

 decreased appetite
 sleep disorders
 depressed mood
 stomach discomfort
 dry mouth
 low white blood cell and/or platelet count, decrease in haemoglobin in your blood, increase in
triglycerides and/or lipase in your blood

 signs or symptoms of inflammation or infection, for example fever, chills, sweats (immune
reactivation syndrome, see section 2 for more details)
45
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects
not listed in this leaflet. You can also report side effects directly via the national reporting system
listed in Appendix V. By reporting side effects you can help provide more information on the safety of
this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date
refers to the last day of that month.
Store in a refrigerator (2°C - 8°C). Do not freeze.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to
throw away medicines you no longer use. These measures will help protect the environment.
What REKAMBYS contains

 The active substance is rilpivirine. Each 2 mL vial contains 600 mg rilpivirine.
 The excipients are poloxamer 338, citric acid monohydrate, glucose monohydrate, sodium
dihydrogen phosphate monohydrate, sodium hydroxide to adjust pH and ensure isotonicity, and
water for injections.
What REKAMBYS looks like and contents of the pack

Prolonged-release suspension for injection. REKAMBYS is presented in a glass vial. The pack also
contains 1 syringe, 1 vial adaptor, and 1 injection needle.
Marketing Authorisation Holder

Turnhoutseweg 30
B-2340 Beerse
Belgium
Manufacturer
Turnhoutseweg 30
B-2340 Beerse
Belgium
For any information about this medicine, please contact the local representative of the Marketing
Authorisation Holder:
België/Belgique/Belgien Lietuva
ViiV Healthcare srl/bv UAB "JOHNSON & JOHNSON"
Tél/Tel: + 32 (0) 10 85 65 00 Tel: +370 5 278 68 88
[email protected]
46
България Luxembourg/Luxemburg
„Джонсън & Джонсън България” ЕООД ViiV Healthcare srl/bv
Тел.: +359 2 489 94 00 Belgique/Belgien
[email protected] Tél/Tel: + 32 (0) 10 85 65 00
Česká republika Magyarország

Janssen-Cilag s.r.o. Janssen-Cilag Kft.
Tel: +420 227 012 227 Tel.: +36 1 884 2858
[email protected]
Danmark Malta
Janssen-Cilag A/S AM MANGION LTD.
Tlf: +45 4594 8282 Tel: +356 2397 6000
[email protected]
Deutschland Nederland
ViiV Healthcare GmbH ViiV Healthcare BV
Tel.: + 49 (0)89 203 0038-10 Tel: + 31 (0) 33 2081199
[email protected]
Eesti Norge
UAB "JOHNSON & JOHNSON" Eesti filiaal Janssen-Cilag AS
Tel: +372 617 7410 Tlf: +47 24 12 65 00
[email protected] [email protected]
Ελλάδα Österreich
Janssen-Cilag Φαρμακευτική Α.Ε.Β.Ε. Janssen-Cilag Pharma GmbH
Tηλ: +30 210 80 90 000 Tel: +43 1 610 300
España Polska
Laboratorios ViiV Healthcare, S.L. Janssen-Cilag Polska Sp. z o.o.
Tel: + 34 900 923 501 Tel.: +48 22 237 60 00
[email protected]
France Portugal
ViiV Healthcare SAS VIIVHIV HEALTHCARE, UNIPESSOAL,
Tél.: + 33 (0)1 39 17 69 69 LDA
[email protected] Tel: + 351 21 094 08 01
[email protected]
Hrvatska România
Johnson & Johnson S.E. d.o.o. Johnson & Johnson România SRL
Tel: +385 1 6610 700 Tel: +40 21 207 1800
[email protected]
Ireland Slovenija
Janssen Sciences Ireland UC Johnson & Johnson d.o.o.
Tel: +353 1 800 709 122 Tel: +386 1 401 18 00
[email protected]
Ísland Slovenská republika

Janssen-Cilag AB Johnson & Johnson s.r.o.
c/o Vistor hf. Tel: +421 232 408 400
Sími: +354 535 7000
[email protected]
47
Italia Suomi/Finland
ViiV Healthcare S.r.l Janssen-Cilag Oy
Tel: +39 045 7741600 Puh/Tel: +358 207 531 300
[email protected]
Κύπρος Sverige
Βαρνάβας Χατζηπαναγής Λτδ Janssen-Cilag AB
Τηλ: +357 22 207 700 Tfn: +46 8 626 50 00
[email protected]
Latvija United Kingdom

UAB "JOHNSON & JOHNSON" filiāle Latvijā ViiV Healthcare UK Limited
Tel: +371 678 93561 Tel: + 44 (0)800 221441
This leaflet was last revised in {MM/YYYY}.
Detailed information on this medicine is available on the European Medicines Agency web site:
http://www.ema.europa.eu/.
48
The following information is intended for medical or healthcare professionals only and should
be read by the medical or healthcare professional in conjunction with the full prescribing
information (Summary of Product Characteristics).
REKAMBYS 2 mL injection Instructions for use:
Overview
A complete dose requires two injections:
2 mL of cabotegravir and 2 mL of rilpivirine.
Cabotegravir and rilpivirine are suspensions that do not need further dilution or reconstitution. The
preparation steps for both medicines are the same.
Cabotegravir and rilpivirine are for intramuscular use only. Both injections must be administered to the
gluteal sites. The administration order is not important.
Note: The ventrogluteal site is recommended.
Storage information
 Store in refrigerator at 2°C to 8°C.
Do not freeze.
Rilpivirine vial Vial adaptor

Vial cap
(Rubber
stopper under
cap)
2 mL
2 mL
Syringe Injection needle
Plunger
Needle guard
Needle cap
Your pack contains

 1 vial of rilpivirine
 1 vial adaptor
 1 syringe
 1 injection needle (23 gauge, 1½ inch)
Consider the patient’s build and use medical judgment to select an appropriate injection needle
length.
49
You will also need
 Non-sterile gloves
 2 alcohol swabs
 2 gauze pads
 A suitable sharps container
 1 cabotegravir 2 mL pack
Make sure to have the cabotegravir pack close by before starting.
Preparation
1. Inspect vial
 Check that the expiry date has not passed.
Check expiry date EXP  Inspect the vials immediately. If you can see
and medicine MONTH/
YEAR foreign matter, do not use the product.
Do not use if the expiry date has passed.
2. Wait 15 minutes
 Wait at least 15 minutes before you are ready
Wait 15 minutes to give the injection to allow the medicine to
come to room temperature.
3. Shake vigorously
 Hold the vial firmly and vigorously shake for
10 a full 10 seconds as shown.
secs  Invert the vial and check the resuspension. It
should look uniform. If the suspension is not
uniform, shake the vial again.
 It is also normal to see small air bubbles.
50
4. Remove vial cap
 Remove the cap from the vial.
 Wipe the rubber stopper with an alcohol swab.
Do not allow anything to touch the rubber

stopper after wiping it.
5. Peel open vial adaptor

 Peel off the paper backing from the vial
adaptor packaging.
Note: Keep the adaptor in place in its

packaging for the next step.
6. Attach vial adaptor

 Press the vial adaptor straight down onto the
vial using the packaging, as shown.
The vial adaptor should snap securely into
place.
 When you are ready, lift off the vial adaptor
packaging as shown.
51
7. Prepare syringe
 Remove the syringe from its packaging.
 Draw 1 mL of air into the syringe. This will
make it easier to draw up the liquid later.
8. Attach syringe
 Hold the vial adaptor and vial firmly, as
shown.
 Screw the syringe firmly onto the vial adaptor.
 Press the plunger all the way down to push the
air into the vial.
9. Slowly draw up dose

 Invert the syringe and vial, and slowly
withdraw as much of the liquid as possible
into the syringe. There might be more liquid
than dose amount.
52
10. Unscrew syringe
 Screw the syringe off the vial adaptor, holding
the vial adaptor as shown.
Note: Keep the syringe upright to avoid

leakage. Check that the suspension looks
uniform and milky white.
11. Attach needle

 Peel open the needle packaging part way to
expose the needle base.
 Keeping the syringe upright, firmly twist the
syringe onto the needle.
 Remove the needle packaging from the
needle.
Injection
12. Prepare injection site
Injections must be administered to the gluteal
sites. Select from the following areas for the
injection:
 Ventrogluteal (recommended)
 Dorsogluteal (upper outer quadrant)
Note: For gluteal intramuscular use only.

Do not inject intravenously.
Ventrogluteal Dorsogluteal
13. Remove cap
 Fold the needle guard away from the needle.
 Pull off the injection needle cap.
53
14. Remove extra liquid
 Hold the syringe with the needle pointing up.
Press the plunger to the 2 mL dose to remove
extra liquid and any air bubbles.
Note: Clean the injection site with an alcohol

2 mL swab. Allow the skin to air dry before
continuing.
15. Stretch skin

Use the z-track injection technique to minimise
medicine leakage from the injection site.
1 inch
(2.5 cm)  Firmly drag the skin covering the injection
site, displacing it by about an inch (2.5 cm).
 Keep it held in this position for the injection.
16. Insert needle

 Insert the needle to its full depth, or deep
enough to reach the muscle.
54
17. Inject dose
 Still holding the skin stretched – slowly press
the plunger all the way down.
 Ensure the syringe is empty.
 Withdraw the needle and release the stretched
skin immediately.
18. Assess the injection site

 Apply pressure to the injection site using a
gauze.
 A small bandage may be used if a bleed
occurs.
Do not massage the area.
19. Make needle safe

 Fold the needle guard over the needle.
 Gently apply pressure using a hard surface to
lock the needle guard in place.
 The needle guard will make a click when it
locks.
click
55
After injection
20. Dispose safely
 Dispose of used needles, syringes, vials and
vial adaptors according to local health and
safety laws.
Repeat for 2nd medicine

If you have not yet injected both medicines, use
the steps for preparation and injection for
Cabotegravir which has its own specific
Instructions for Use.
Repeat all steps

for 2nd medicine
56
Questions and Answers
1. How long can the medicine be left out of the refrigerator?
It is best to inject the medicine as soon as it reaches room temperature. However, the vial may sit in the
carton at room temperature (maximum temperature of 25°C) for up to 6 hours.
2. How long can the medicine be left in the syringe?

It is best to inject the (room temperature) medicine as soon as possible after drawing it up. However, the
medicine can remain in the syringe for up to 2 hours before injecting.
If 2 hours are exceeded, the medicine, syringe and needle must be discarded.
3. Why do I need to inject air into the vial?

Injecting 1 mL of air into the vial makes it easier to draw up the dose into the syringe. Without the air,
some liquid may flow back into the vial unintentionally, leaving less than intended in the syringe.
4. Does the order in which I give the medicines matter?

No, the order is unimportant.
5. Is it safe to warm the vial up to room temperature more quickly?

It is best to let the vial come to room temperature naturally. However, you can use the warmth of your
hands to speed up the warm up time, but make sure the vial does not get above 25°C.
Do not use any other heating methods.
6. Why is the ventrogluteal administration approach recommended?

The ventrogluteal approach, into the gluteus medius muscle, is recommended because it is located away
from major nerves and blood vessels. A dorso-gluteal approach, into the gluteus maximus muscle, is
acceptable, if preferred by the healthcare professional. The injection should not be administered in any
other site.
57
Package leaflet: Information for the user
rilpivirine
Read all of this leaflet carefully before you start taking this medicine because it contains
important information for you.
- Keep this leaflet. You may need to read it again.
- If you have any further questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not pass it on to others. It may harm them,
even if their signs of illness are the same as yours.
- If you get any side effects, talk to your doctor or pharmacist. This includes any possible side
effects not listed in this leaflet. See section 4.
What is in this leaflet

1. What is REKAMBYS and what it is used for
1. What REKAMBYS is and what it is used for
REKAMBYS contains the active ingredient rilpivirine. It is one of a group of medicines called
non-nucleoside reverse transcriptase inhibitors (NNRTIs) that are used for the treatment of human
immunodeficiency virus type 1 (HIV-1) infection.
REKAMBYS works together with other HIV medicines to block the ability of the virus to make more
copies of itself. REKAMBYS injections do not cure HIV infection but help reduce the amount of HIV
in your body and keeps it at a low level. This holds off damage to the immune system and the
development of infections and diseases associated with AIDS.
REKAMBYS is always given with another HIV medicine called cabotegravir injection. They are used
together in adults aged 18 years and older whose HIV-1 infection is already under control.
Do not use REKAMBYS if you are allergic to rilpivirine or any of the other ingredients of this
medicine (listed in section 6).
prevent seizures)
tuberculosis)
depression).
Warnings and precautions

Talk to your doctor or pharmacist before using REKAMBYS.
58
REKAMBYS is not a cure for HIV infection. It is part of a treatment to reduce the amount of virus in
the blood. You can still pass on HIV when using this medicine, although the risk is lowered by
effective antiretroviral therapy. Discuss with your doctor the precautions you need to take to avoid
infecting other people.
Tell your doctor about your situation

Check the following points and tell your doctor if any of them apply to you.
- You must attend all the planned visits for injections, do not miss any visits, it is very important
for the success of your treatment. If you cannot attend a planned visit, inform your doctor as
soon as possible.
- Tell your doctor if you have ever had problems with your liver, including hepatitis B or
hepatitis C, or problems with your kidneys. Your doctor may check how well your liver or
kidneys work to decide if you can use REKAMBYS. See ‘Uncommon side effects’ in section 4
of this leaflet for signs of liver damage.
- Tell your doctor immediately if you notice any symptoms of infections (for example, fever,
chills, sweats). In some patients with HIV, inflammation from previous infections may occur
soon after starting HIV treatment. It is believed that these symptoms are due to an improvement
in the body’s immune response, enabling the body to fight infections that were present
previously but caused no obvious symptoms.
- Also tell your doctor straight away if you notice any symptoms such as muscle weakness,
weakness beginning in the hands and feet and moving up towards the trunk of the body,
palpitations, tremor or hyperactivity. This is because autoimmune disorders (conditions in
which the immune system mistakenly attacks healthy body tissue) may also occur after you start
taking medicines for the treatment of your HIV infection. Autoimmune disorders may occur
many months after the start of treatment.
- Tell your doctor if you are taking any medicines that you have been told may cause a life-
threatening irregular heartbeat (torsade de pointes).
Reactions to Injections
Post-injection reaction symptoms have happened within minutes in some people after receiving their
rilpivirine injection. Most symptoms resolved within a few minutes after the injection. Symptoms of
post-injection reactions may include: difficulty breathing, stomach cramps, sweating, numbness of
your mouth, feeling anxious, feeling warm, feeling lightheaded or feeling like you are going to pass
out (faint), and blood pressure changes. Tell your healthcare professional if you experience these
symptoms after you receive your injections.
Regular appointments are important

It is important that you attend your planned appointments to receive REKAMBYS, to control your
HIV infection and to stop your illness from getting worse. Do not miss any visits, it is very important
for the success of your treatment. If you cannot attend a planned visit, inform your doctor as soon as
possible. Talk to your doctor if you are thinking about stopping treatment. If you are late receiving
your REKAMBYS injection, or if you stop receiving REKAMBYS, you will need to take other
medicines to treat HIV infection and to reduce the risk of the virus becoming resistant as the drug
levels in your body will be too low to treat the HIV infection.
Children
REKAMBYS is not for use in children and adolescents less than 18 years of age, because it has not
been studied in these patients.
Other medicines and REKAMBYS

Tell your healthcare provider if you are taking, have recently taken or might take any other medicines.
Some medicines may affect the levels of REKAMBYS in the blood if you are taking them while being
treated with REKAMBYS, or REKAMBYS may affect how well the other medicine works.
59
prevent seizures)
tuberculosis)
depression).
The effects of REKAMBYS or other medicines might change if you use REKAMBYS together
with any of the following medicines:
- clarithromycin, erythromycin (antibiotics)
- methadone (used to treat narcotic withdrawal and dependence)
Pregnancy and breast-feeding

Tell your doctor immediately if you are pregnant or if you plan to become pregnant. Your doctor will
consider the benefit and the risk to you and your baby of using REKAMBYS while you are pregnant.
If you are planning to have a baby, talk to your doctor in advance, as rilpivirine can remain in your
body for up to 4 years after the last injection of REKAMBYS.
Women who have HIV must not breast-feed because HIV may pass into breast milk and infect the
baby.
Ask your doctor or pharmacist for advice before taking any medicine.
Driving and using machines

Some patients may feel tired, dizzy or drowsy during treatment with REKAMBYS. Do not drive or
operate machinery if you have any of these side effects.
Important information about some of the ingredients of REKAMBYS

This medicine contains less than 1 mmol sodium (23 mg) per 3 mL injection, that is to say essentially
‘sodium-free’.
A nurse or doctor will give you REKAMBYS as an injection in the muscle of your buttock
(intramuscular, or IM injection).
You will be given your injection either once every month or once every 2 months, together with
another injectable medicine called cabotegravir. Your doctor will explain how often the medicine will
be given.
Before you start treatment with REKAMBYS, your doctor will prescribe you daily treatment with
rilpivirine and cabotegravir tablets for one month. This is called the lead-in period - taking the tablets
before you receive REKAMBYS and cabotegravir injections will allow your doctor to test how well
these medicines suit you.
60
If you are going to be given REKAMBYS every month, your treatment will be as follows:
When
month of tablets)
Rilpivirine 25-mg tablet once daily single injection of 600 mg by injection every
900 mg month
Cabotegravir 30-mg tablet once daily single injection of 400 mg by injection every
600 mg month
If you are going to be given REKAMBYS every 2 months, your treatment will be as follows:
When
month of tablets)
and month 3
Rilpivirine 25-mg tablet, once daily single injection of 900 mg by injection, every
900 mg 2 months
Cabotegravir 30-mg tablet, once daily single injection of 600 mg by injection, every
600 mg 2 months
If you miss a REKAMBYS injection

It is important that you keep your regular planned appointments to receive your injection. If you miss
an appointment, contact your doctor immediately to make a new appointment.
Talk to your doctor if you think you will not be able to receive your REKAMBYS injection at the
usual time. Your doctor may recommend you take tablets instead, until you are able to have a
REKAMBYS injection again.
If you are given too much REKAMBYS

A doctor or nurse will give this medicine to you, so it is unlikely that you will be given too much. If
you are worried, tell the doctor or nurse.
Don’t stop using REKAMBYS without advice from your doctor.

Use REKAMBYS for as long as your doctor recommends. Don’t stop unless your doctor advises you
to.
Low levels of rilpivirine (the active ingredient of REKAMBYS) can remain in your body for up to
4 years after stopping treatment. However, once you received your last REKAMBYS injection, the
low levels of rilpivirine that remain will not work well enough against the virus which then can
become resistant. To keep your HIV-1 infection under control and to stop the virus becoming resistant,
you must start a different HIV treatment by the time your next REKAMBYS injection was planned.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following is a list of side effects that have been reported when REKAMBYS is used with
cabotegravir injection.
Very common side effects (affects at least 1 in 10 people)

 headache
 injection site reactions - these are generally mild to moderate and became less frequent over
time. Symptoms may include:
o very common: pain and discomfort, a hardened mass or lump
61
o common: redness, itching, swelling, bruising, warmth or discoloration.
o uncommon: numbness, minor bleeding, an abscess (collection of pus) or cellulitis (heat,
swelling or redness).
 feeling hot/feverish (pyrexia)

 depression
 anxiety
 abnormal dreams
 sleeping difficulty (insomnia)
 dizziness
 feeling sick (nausea)
 vomiting
 belly pain (abdominal pain)
 wind (flatulence)
 diarrhoea
 rash
 muscle pain (myalgia)
 tiredness (fatigue)
 feeling weak (asthenia)
 generally feeling unwell (malaise)
 weight gain

 feeling drowsy (somnolence)
 feeling lightheaded, during or after an injection. This may lead to fainting.
 liver damage (signs may include yellowing of the skin and the whites of the eyes loss of
appetite, itching, tenderness in the belly, light-coloured stools or unusually dark urine).
 changes in liver blood tests (increase in transaminases)
 an increase in bilirubin (a substance produced by the liver) in the blood.
Other side effects

 Severe abdominal pain caused by inflammation of the pancreas (pancreatitis).
The following side effects that can occur with rilpivirine tablets may also occur with REKAMBYS
injection:
Very Common side effects

 increase in cholesterol and/or pancreatic amylase in your blood

 decreased appetite
 sleep disorders
 depressed mood
 stomach discomfort
 dry mouth
 low white blood cell and/or platelet count, decrease in haemoglobin in your blood, increase in
triglycerides and/or lipase in your blood

 signs or symptoms of inflammation or infection, for example fever, chills, sweats (immune
reactivation syndrome, see section 2 for more details)
62
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects
not listed in this leaflet. You can also report side effects directly via the national reporting system
listed in Appendix V. By reporting side effects you can help provide more information on the safety of
this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date
refers to the last day of that month.
Store in a refrigerator (2°C - 8°C). Do not freeze.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to
throw away medicines you no longer use. These measures will help protect the environment.
What REKAMBYS contains

 The active substance is rilpivirine. Each 3 mL vial contains 900 mg rilpivirine
 The excipients are poloxamer 338, citric acid monohydrate, glucose monohydrate, sodium
dihydrogen phosphate monohydrate, sodium hydroxide to adjust pH and ensure isotonicity, and
water for injections.
What REKAMBYS looks like and contents of the pack

Prolonged-release suspension for injection. REKAMBYS is presented in a glass vial. The pack also
contains 1 syringe, 1 vial adaptor, and 1 injection needle.
Marketing Authorisation Holder

Turnhoutseweg 30
B-2340 Beerse
Belgium
Manufacturer
Turnhoutseweg 30
B-2340 Beerse
Belgium
For any information about this medicine, please contact the local representative of the Marketing
Authorisation Holder:
België/Belgique/Belgien Lietuva
ViiV Healthcare srl/bv UAB "JOHNSON & JOHNSON"
Tél/Tel: + 32 (0) 10 85 65 00 Tel: +370 5 278 68 88
[email protected]
63
България Luxembourg/Luxemburg
„Джонсън & Джонсън България” ЕООД ViiV Healthcare srl/bv
Тел.: +359 2 489 94 00 Belgique/Belgien
[email protected] Tél/Tel: + 32 (0) 10 85 65 00
Česká republika Magyarország

Janssen-Cilag s.r.o. Janssen-Cilag Kft.
Tel: +420 227 012 227 Tel.: +36 1 884 2858
[email protected]
Danmark Malta
Janssen-Cilag A/S AM MANGION LTD.
Tlf: +45 4594 8282 Tel: +356 2397 6000
[email protected]
Deutschland Nederland
ViiV Healthcare GmbH ViiV Healthcare BV
Tel.: + 49 (0)89 203 0038-10 Tel: + 31 (0) 33 2081199
[email protected]
Eesti Norge
UAB "JOHNSON & JOHNSON" Eesti filiaal Janssen-Cilag AS
Tel: +372 617 7410 Tlf: +47 24 12 65 00
Ελλάδα Österreich
Janssen-Cilag Φαρμακευτική Α.Ε.Β.Ε. Janssen-Cilag Pharma GmbH
Tηλ: +30 210 80 90 000 Tel: +43 1 610 300
España Polska
Laboratorios ViiV Healthcare, S.L. Janssen-Cilag Polska Sp. z o.o.
Tel: + 34 900 923 501 Tel.: +48 22 237 60 00
[email protected]
France Portugal
ViiV Healthcare SAS VIIVHIV HEALTHCARE, UNIPESSOAL,
Tél.: + 33 (0)1 39 17 69 69 LDA
[email protected] Tel: + 351 21 094 08 01
[email protected]
Hrvatska România
Johnson & Johnson S.E. d.o.o. Johnson & Johnson România SRL
Tel: +385 1 6610 700 Tel: +40 21 207 1800
[email protected]
Ireland Slovenija
Janssen Sciences Ireland UC Johnson & Johnson d.o.o.
Tel: +353 1 800 709 122 Tel: +386 1 401 18 00
[email protected]
Ísland Slovenská republika

Janssen-Cilag AB Johnson & Johnson s.r.o.
c/o Vistor hf. Tel: +421 232 408 400
Sími: +354 535 7000
[email protected]
64
Italia Suomi/Finland
ViiV Healthcare S.r.l Janssen-Cilag Oy
Tel: +39 045 7741600 Puh/Tel: +358 207 531 300
[email protected]
Κύπρος Sverige
Βαρνάβας Χατζηπαναγής Λτδ Janssen-Cilag AB
Τηλ: +357 22 207 700 Tfn: +46 8 626 50 00
[email protected]
Latvija United Kingdom

UAB "JOHNSON & JOHNSON" filiāle Latvijā ViiV Healthcare UK Limited
Tel: +371 678 93561 Tel: + 44 (0)800 221441
This leaflet was last revised in {MM/YYYY}.
Detailed information on this medicine is available on the European Medicines Agency web site:
http://www.ema.europa.eu/.
65
The following information is intended for medical or healthcare professionals only and should
be read by the medical or healthcare professional in conjunction with the full prescribing
information (Summary of Product Characteristics).
REKAMBYS 3 mL injection Instructions for use:
Overview
A complete dose requires two injections:
3 mL of cabotegravir and 3 mL of rilpivirine.
Cabotegravir and rilpivirine are suspensions that do not need further dilution or reconstitution. The
preparation steps for both medicines are the same.
Cabotegravir and rilpivirine are for intramuscular use only. Both injections must be administered to the
gluteal sites. The administration order is not important.
Note: The ventrogluteal site is recommended.
Storage information
• Store in refrigerator at 2°C to 8°C.
Do not freeze.
Rilpivirine vial Vial adaptor

Vial cap
(Rubber
stopper
under cap)
2 mL
2 mL
Syringe Injection needle
Plunger
Needle guard
Needle cap
Your pack contains

 1 vial of rilpivirine
 1 vial adaptor
 1 syringe
 1 injection needle (23 gauge, 1½ inch)
Consider the patient’s build and use medical judgment to select an appropriate injection needle
length.
66
You will also need
 Non-sterile gloves
 2 alcohol swabs
 2 gauze pads
 A suitable sharps container
 1 cabotegravir 3 mL pack
 Make sure to have the cabotegravir pack close by before starting.
Preparation
1. Inspect vial
 Check that the expiry date has not passed.
Check expiry date EXP  Inspect the vials immediately. If you can see
and medicine MONTH/
YEAR foreign matter, do not use the product.
Do not use if the expiry date has passed.
2. Wait 15 minutes
 Wait at least 15 minutes before you are ready
Wait 15 minutes to give the injection to allow the medicine to
come to room temperature.
3. Shake vigorously
 Hold the vial firmly and vigorously shake for
10 a full 10 seconds as shown.
secs  Invert the vial and check the resuspension. It
should look uniform. If the suspension is not
uniform, shake the vial again.
 It is also normal to see small air bubbles.
67
4. Remove vial cap
 Remove the cap from the vial.
 Wipe the rubber stopper with an alcohol swab.
Do not allow anything to touch the rubber

stopper after wiping it.
5. Peel open vial adaptor

 Peel off the paper backing from the vial
adaptor packaging.
Note: Keep the adaptor in place in its

packaging for the next step.
6. Attach vial adaptor

 Press the vial adaptor straight down onto the
vial using the packaging, as shown.
The vial adaptor should snap securely into
place.
 When you are ready, lift off the vial adaptor
packaging as shown.
68
7. Prepare syringe
 Remove the syringe from its packaging.
 Draw 1 mL of air into the syringe. This will
make it easier to draw up the liquid later.
8. Attach syringe
 Hold the vial adaptor and vial firmly, as
shown.
 Screw the syringe firmly onto the vial adaptor.
 Press the plunger all the way down to push the
air into the vial.
9. Slowly draw up dose

 Invert the syringe and vial, and slowly
withdraw as much of the liquid as possible
into the syringe. There might be more liquid
than dose amount.
69
10. Unscrew syringe
 Screw the syringe off the vial adaptor, holding
the vial adaptor as shown.
Note: Keep the syringe upright to avoid

leakage. Check that the suspension looks
uniform and milky white.
11. Attach needle

 Peel open the needle packaging part way to
expose the needle base.
 Keeping the syringe upright, firmly twist the
syringe onto the needle.
 Remove the needle packaging from the
needle.
Injection
12. Prepare injection site
Injections must be administered to the gluteal
sites. Select from the following areas for the
injection:
 Ventrogluteal (recommended)
 Dorsogluteal (upper outer quadrant)
Note: For gluteal intramuscular use only.

Do not inject intravenously.
Ventrogluteal Dorsogluteal
70
13. Remove cap
 Fold the needle guard away from the needle.
 Pull off the injection needle cap.
14. Remove extra liquid

 Hold the syringe with the needle pointing up.
Press the plunger to the 3 mL dose to remove
extra liquid and any air bubbles.
Note: Clean the injection site with an alcohol

swab. Allow the skin to air dry before
3 mL continuing.
15. Stretch skin

Use the z-track injection technique to minimise
medicine leakage from the injection site.
1 inch
(2.5 cm)  Firmly drag the skin covering the injection
site, displacing it by about an inch (2.5 cm).
 Keep it held in this position for the injection.
16. Insert needle

 Insert the needle to its full depth, or deep
enough to reach the muscle.
71
17. Inject dose
 Still holding the skin stretched – slowly press
the plunger all the way down.
 Ensure the syringe is empty.
 Withdraw the needle and release the stretched
skin immediately.
18. Assess the injection site

 Apply pressure to the injection site using a
gauze.
 A small bandage may be used if a bleed
occurs.
Do not massage the area.
19. Make needle safe

 Fold the needle guard over the needle.
 Gently apply pressure using a hard surface to
lock the needle guard in place.
 The needle guard will make a click when it
locks.
click
72
After injection
20. Dispose safely
 Dispose of used needles, syringes, vials and
vial adaptors according to local health and
safety laws.
Repeat for 2nd medicine

If you have not yet injected both medicines, use
the steps for preparation and injection for
Cabotegravir which has its own specific
Instructions for Use.
Repeat all steps

for 2nd medicine
Questions and Answers

1. How long can the medicine be left out of the refrigerator?
It is best to inject the medicine as soon as it reaches room temperature. However, the vial may sit in the
carton at room temperature (maximum temperature of 25°C) for up to 6 hours.
2. How long can the medicine be left in the syringe?

It is best to inject the (room temperature) medicine as soon as possible after drawing it up. However, the
medicine can remain in the syringe for up to 2 hours before injecting.
If 2 hours are exceeded, the medicine, syringe and needle must be discarded.
3. Why do I need to inject air into the vial?

Injecting 1 mL of air into the vial makes it easier to draw up the dose into the syringe. Without the air,
some liquid may flow back into the vial unintentionally, leaving less than intended in the syringe.
4. Does the order in which I give the medicines matter?

No, the order is unimportant.
5. Is it safe to warm the vial up to room temperature more quickly?

It is best to let the vial come to room temperature naturally. However, you can use the warmth of your
hands to speed up the warm up time, but make sure the vial does not get above 25°C.
Do not use any other heating methods.
6. Why is the ventrogluteal administration approach recommended?

The ventrogluteal approach, into the gluteus medius muscle, is recommended because it is located away
73
from major nerves and blood vessels. A dorso-gluteal approach, into the gluteus maximus muscle, is
acceptable, if preferred by the healthcare professional. The injection should not be administered in any
other site.
74

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ANNEX I

SUMMARY OF PRODUCT CHARACTERISTICS

REKAMBYS 600 mg prolonged-release suspension for injection

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

For the full list of excipients, see section 6.1.

Prolonged-release suspension for injection

4.1 Therapeutic indications

4.2 Posology and method of administration

Following discontinuation of REKAMBYS in combination with cabotegravir injection, it is

Continuation injection (600 mg corresponding to 2 mL)

Every 2 months dosing

Continuation Injections – 2 months apart (900 mg corresponding to 3 mL)

Cabotegravir 30 mg once daily 600 mg monthly 600 mg every 2 months

Dosing Recommendations When Switching From Monthly to Every 2 Months Injections

Dosing Recommendations When Switching From Every 2 Months to Monthly Injections

For intramuscular use.

REKAMBYS should be administered by a healthcare professional. For instructions on administration,

REKAMBYS should always be co-administered with a cabotegravir injection. REKAMBYS and

Injections must be administered to the ventrogluteal (recommended) or the dorsogluteal sites.

4.4 Special warnings and precautions for use

Risk of resistance following treatment discontinuation

If virologic failure is suspected, an alternative regimen should be adopted as soon as possible.

Baseline factors associated with virological failure

Interactions with other medicinal products

Immune reactivation syndrome

Medicinal products that affect rilpivirine exposure

Medicinal products that are affected by the use of rilpivirine

Table 5: Interactions and dose recommendations with other medicinal products

(induction of CYP3A due to high

rilpivirine AUC ↑ 49%

(inhibition of CYP3A enzymes)

(inhibition of CYP3A enzymes)

300 mg once daily rilpivirine AUC ↑ 16%*

* compared to 25 mg once daily rilpivirine

(induction of CYP3A enzymes)

(induction of CYP3A enzymes)

(inhibition of CYP3A enzymes)

QT prolonging medicinal products

4.6 Fertility, pregnancy and lactation

The effect of REKAMBYS on human pregnancy is unknown.

Animal studies do not indicate reproductive toxicity (see section 5.3).

4.7 Effects on ability to drive and use machines

Summary of the safety profile

Tabulated summary of adverse reactions

Table 6: Tabulated summary of adverse reactions1

Hepatobiliary disorders Uncommon hepatotoxicity

Local Injection Site Reactions (ISRs)

Changes in laboratory chemistry

Reporting of suspected adverse reactions

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: Antiviral for systemic use, non-nucleoside reverse transcriptase

Rilpivirine is a diarylpyrimidine non-nucleoside reverse-transcriptase inhibitor (NNRTI) of HIV-1.

Antiviral activity in vitro

Virologically suppressed patients:

Site-directed NNRTI mutant virus

Recombinant clinical isolates

Virologically suppressed patients

Clinical efficacy and safety

Every 1 month dosing