3rd World ADC Asia Brochure
3rd World ADC Asia Brochure
3rd World ADC Asia Brochure
WELCOME
APRIL 26
3rdANNUAL
EXPERT SPEAKERS
ASIA 2024
AGENDA
Development in Asia
PARTNER WITH US
Ziping Wei Yasuyuki Kaneta Jun Ge
Chief Executive Senior Director Executive Director,
Officer Daiichi Sankyo Head of China
Bliss Biopharma Clinical Development
Gilead
WELCOME
Incheon, South Korea
Based in Asia
Why Your Peers Are
Looking Forward to the
The year 2024 has been considered the ‘coming of age’ era for antibody-drug conjugates, Conference:
in great part due to the remarkable resurgence in drug development across the Asia-
Pacific region. The massive increase in the quantity of new ADC programs from Asian
Having a chance to meet
developers has been especially noticeable since 2022, with the number of ADCs in the with like-minded colleagues
clinic surpassing those being developed the United States for the fifth year in a row. This, in the industry to discuss
alongside multiple high-profile deals in the region, is making all eyes turn towards Asia ADC drug development is
for the next blockbuster ADC. rare. We look forward to
EXPERT SPEAKERS
Returning by popular demand after a short break, the 3rd World ADC Asia will engaging, be invigorated and
be bringing together pioneers and key opinion leaders across mega-pharma and inspired
biotechnology focusing on China, Japan, Taiwan, South Korea and Singapore this
June.
Heidi Wang, Chief Executive
Officer, OBI Pharma
There has never been a stronger time for antibody-drug conjugate development in Asia.
This is shown by the Japanese born Enhertu reaching blockbuster status, Asia accounting I am excited to be part of
for half of the new ADC clinical trials in 2023, and some of the biggest ADC deals this meeting to learn about
occurring across APAC. Join the ADC community based in this region to discuss the
the latest advancements
most pressing Asian-specific challenges, learn from recent innovations, and meet
long-standing experts from the west to create partnerships that can propel your ADC and innovations in the field
further than ever before. of ADC, to network with
peers, particularly in Asia,
Be in the room when the east meets the west across three packed days with the highest
-quality industry speakers including Daiichi Sankyo, Eisai, Shanghai Miracogen, and to share our research
PinotBio, Orum Therapeutics, Pfizer, and more. Backed by 14 years of experience and insights
providing insights to the global ADC community, World ADC will connect you with those Mike Liao, Global Clinical
AGENDA
leading the way in innovation.
Pharmacology Lead –
Whether you are a CEO, Managing Director, Head of Lab, or Scientist, this is the meeting Oncology, Genentech
for you to get the most up to date knowledge about what is happening with ADCs in Asia.
Gain a Learn about novel Navigate varying Understand the Explore the PARTNER WITH US
comprehensive innovation in ADC governing development of importance of
overview of technologies guidance to DXd technology revolutionary
clinical updates coming out of Asia ensure regulatory and the conjugation
and main such as “CHO- harmonization to latest clinical technology in
aspects of clinical TEM”, bispecific gain IND approval developments of CMC development
development in ADCs, stroma and kickstart your early DXd assets to improve
China, as well targeting ADCs, clinical trials with with Daiichi manufacturing
REGISTER YOUR PLACE
WELCOME
Incheon, South Korea
With the constant deals, innovations and collaborations With ADC news dominating the headlines, it might be
in the space, all eyes are turning towards Asia for the hard to keep track of all the new developments. This
next big thing when it comes to ADC development. By is your executive summary illustrating the existing
breaking through the biosimilars and looking towards opportunities and current state of the ADC Asian Market,
novel payloads, conjugation technologies, linkers, and most recent news. Brought closer to your home, the 3rd
more this region of the world is leading the charge on World ADC Asia is your industry touchpoint to discuss
EXPERT SPEAKERS
antibody-drug conjugate innovation. novel technolgies, understand regulatory guidance, hone
strategic collaborations, and most importantly, accelerate
the development of the next asian-based approved ADC.
60 60
Asia Europe United States
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Number of Drugs
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AGENDA
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United States
China
South Korea
Singapore
Japan |
India
United Kingdom
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Netherlands
Denmark
Italy
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Czech Republic
France
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Everyone wants Daiichi Sankyo Samsung Eisai’s cancer Ajinomoto and JPM23:
an ADC: GSK and Merck Biologics moves drug Halaven Exelixis partner Samsung
up plans to open
pays US$85M announce global its US$1.5B+
at the center of to develop novel plans to kick
upfront for development plant. The CDMO US$2B pact with antibody-drug off antibody-
ex-China rights and commer- also has plans Bliss Bio, like conjugates drug conjugate
to Hansoh cialization to expand its its Bristol Myers for cancer manufacturing in
Pharma’s collaboration antibody-drug ADC deal treatment early 2024
conjugates
antibody-drug for three Daiichi business by
(May 2023) (Jan 2023) (Jan 2023)
conjugate Sankyo Dxd building an ADC
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ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
Dhiraj Gambhire Yasuyuki Kaneta Masayuki Miyano
Executive Director, Senior Director Principal Scientist
Global Clinical Daiichi Sankyo Eisai
Development
Daiichi Sankyo
AGENDA
Tse Wen Chang Zaiqi Wang Stephen Slocum
Founder & Chairman Chief Executive Officer Director of Drug Development
Immunwork Inxmed LegoChem Biosciences
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James Palacino Vivian Trang Hyun Yong Cho
Senior Vice President & Principal Scientist Chief Scientific Officer
Head of Research Pfizer PinotBio
Orum Therapeutics
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
Workshop A 9.00
EXPERT SPEAKERS
The biggest roadblock in developing ADCs in Asia is not having enough Workshop Leaders
regulatory guidance from other agencies. This is especially important when trying
Heidi Wang
to run clinical trials in multiple countries while adhering to varying regulatory guidelines. Chief Executive
This interactive session will give you a holistic overview of varying governmental Officer
regulations and how to follow them to confidently meet expectations from agencies. OBI Pharma
Join this workshop to:
• Understand how to jump over regulatory hurdles in the APAC region
• Examine the differing regulatory requirements of the FDA, EMA, NMPA, and more Dhiraj Gambhire
• Assess the best way to gain IND approval to kickstart your clinical trials Executive Director,
Global Clinical
• Analyze regulatory expectations from a CMC aspect Development
• Focus on regulatory harmonization across the globe Daiichi Sankyo
AGENDA
Workshop B 1.00
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Join this workshop to:
• Understand how global partnerships can open up global rights for development and
commercialization
• Evaluate what makes a company a good partner- is it an ADC in the clinic? Novel Paul Song
propriety technology? Chief Scientific
Officer
• Determine the potential bigger pharma have and what value you can bring to the table
Genequantum
• Navigate different cultures and ways of working to harbor stronger relationships Healthcare
• Enhance communication with mega pharma
Shanshan Xu
Vice President,
External
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Innovations
BioNTech
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
Outlining Clinical Updates & Clinical Progression in Field to Ensure a Smooth Translation
Into the Clinic
8.30 Exploring the Clinical Results of MRG003 & MRG004A to Develop EFGR
Ziye Sui Targeted ADCs
Chief Executive Officer • Comprehensive review of five ADCs currently in clinical studies
Shanghai Miracogen/ • Outline updated clinical results on nasopharyngeal carcinoma and HNSCC for MRG003,
Lepu Biopharma an EGFR targeted ADC
• Gain a clinical update for MRG004A, a TF targeted ADC
AGENDA
9.00 From Product to Platform: Henlius’ Practices & Progress in ADC to
Shan Yongqiang Address Unmet Medical Needs
General Manager,
Global Innovation • Review how ADC is a strategic R&D field of Henlius based on its 13+ year antibody
Centre capabilities and integrated R&D platform
Henlius Biotech • Explore the highlights of ADC assets’ progress in clinical and pre-clinical stages
• Learn how Henlius is dedicated in building ADC platform - “Hanjugator”
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• Discuss how identifying the best combination of antibody, linker and payload is a
challenge that can be overcome by applying stage-specific evaluation criteria to de-risk
ADC candidate selection
• Review case studies showing how to construct and evaluate appropriate ADC candidate
matrices, varying payloads, and linker elements for lead candidate selection
11.00 Exploring ADCs With Site-Specific Conjugation, DAR of 8 or 12, & Payloads
With Dual Drugs to Turbocharge ADC Innovation
Hsing-Mao Chu • Discuss the “CHO-TEM” technology, combining CHO Pharma’s “glycan modification”
Chief Executive Officer technology, and T-E Meds’ “drug bundles” technology
T-E Meds • Outline how antibody molecule glycans are modified with one enzyme to create 4 azido
groups, to which 4 drug bundles each with 2 or 3 drugs of two categories are linked
• Learn how to produce homogeneous ADCs with high DAR (8 or 12), and dual drugs
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
12.00 Addressing the Complexity of Manufacturing ADCs From Early Stage to
Commercial
• Outlining key challenges related to breakthrough and fast approval designation
• Discussing methods to build a robust technical package to support a consistent
regulatory strategy
• Delivering important updates on conjugation and fill-finish capacity
1.30 Exploring the Advantages of Using Bispecific ADCs & Their Impact on
Jinwon Jung Efficacy & Toxicity to Increase Patient Treatability
Senior Director • Discuss proof of concept study of a bispecific ADC
ABL Bio • Review the recent development progress of a bispecific ADC
• Assess the benefit of bispecific ADC in terms of efficacy and toxicity
AGENDA
2.00 Reviewing the Development of DXd ADC Technology & the Latest
Clinical Results
Yasuyuki Kaneta
Senior Director • Gain an overview of the DXd-ADC technology platform
Daiichi Sankyo • Receive updates on clinical development of T-DXd
• Discuss updates on preclinical and clinical development of early DXd assets, such as
R-DXd, DS-3939, etc.
2.30 Exploring the OBI Pharma ADC Assets & the GlycOBI™ Platform
• Discover how OBI Pharma has developed a unique glycan ADC platform (GlycOBI™) to
enable a site-specific conjugation, which is in a ‘Plug and Play’ format and compatible
Heidi Wang
with any antibodies, linkers, and payloads in various DAR
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Chief Executive Officer
OBI Pharma • Review how assets using the GlycOBI™ platform have the potential for improved in vivo
efficacy, better safety profile, and enhanced stability in animal studies
• Share data about how Anti-Nectin-4, -TROP2, HER2, and bi-specific ADCs were
developed based on OBI’s GlycOBI™ platform
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
Exploring Global Manufacturing Capabilities & the Challenges With Antibody & Linker-
Payload Supply Chain to Reduce Process Complexity & Standardize ADC Development
5.00 Panel Discussion: Mastering Supply Chain Issues in Sourcing Antibodies, Linkers & Payloads to Asia to
Plan Ahead & Reduce Lead Times
• Understanding why supply chain is a bigger problem in the APAC region
• Dealing with a different time zone: the pros and cons
• Navigating the difficulty of accessing the European and American markets
AGENDA
Chief Technology Development & GMP Manufacturing of ADC Therapeutics
Officer • Discuss integrated conjugation manufacturing platform
Genequantum • Review a continuous conjugation manufacturing process
Healthcare • Outline a quality control strategy
Mingjiu Chen
Chief Executive Officer 6.00 Chair’s Closing Remarks
Biosion
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6.15 End of Scientific Program Day One
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
Nitin Damle
Executive Vice
President & Chief
Innovation Officer Chair’s Opening Remarks
EXPERT SPEAKERS
7.50
Sun Pharma
Advanced Research
Company
Identifying Novel Targets & Their Benefits to Diversify ADC Programs & Design a More
Accurate ADC
8.00 Unmet Needs in ADCs for Gastrointestinal Cancer: East-West Differences &
Seung-Jae Myung Novel Target Strategies Beyond HER2 & TROP2
Chief Executive Officer • Addressing the unmet needs of ADCs in gastrointestinal cancers
EDIS Biotech • Discussing the regional differences in the need for an ADC for gastrointestinal cancers
• Going beyond HER2 and TROP2: Novel targets for ADCs in gastrointestinal cancers
8.30 Developing a Precise ADC for Novel Targets to Take Your ADC From Bench
AGENDA
Do-Hyun Nam to Bedside
Chairman • Exploring target discovery for ADCs
Aimed Bio • Understanding pre-clinical and clinical translation
• Developing the best-in-class ADC for precision oncology
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9.30 Versatile & Robust Chemical Site-Specific Conjugation Platform: AJICAP®
Technology
• AJICAP®️ Conjugation: Examining how site-specific technologies are being employed
in many of the next-generation ADCs due to the enhancement of clinically relevant
biological properties observed in various preclinical studies
• AJICAP®️ Linker: Demonstrating a novel hydrophilic linker technology that enables the
versatile synthesis of homogenous DAR = 1, 2, 4, 8, and higher
• Showcasing Bispecific and Trispecific antibodies produced by fully-chemical
conjugation technology
11.00 NN3201, a Novel C-Kit Targeting ADC, Exhibits Robust Preclinical Anti-
Sun-Hwa Lee Tumor Efficacy in SCLC & GIST Models
Vice Chief Scientific
Officer • Navigating the effects of NN3201 in small cell lung cancer
Novelty Nobility • Exploring a novel C-Kit targeting ADC
• Showing anti-tumor efficacy in SCLC and GIST models
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
• Understanding pancreatic cancer and its effects
• Reviewing a novel payload, BET protein degrader
12.00 From Concept to Market: Accelerating ADC Development With WuXi XDC’s
Fully Integrated Discovery & CMC Platforms
• Showcasing the one-stop integrated discovery service platform focusing on bioconjugate
lead selection that includes mAb/protein generation, payload linker synthesis,
bioconjugate preparation, in vitro and in vivo characterization
• Demonstrating fully integrated ADC CMC development and manufacturing with industry
leading DNA to IND timeline of 15 months; mAb/payload-linker/conjugation DS & DP all by
in-house team and facilities
• Sharing vast ADC experience with 250+ discovery projects, 75+ CMC projects, 27+ INDs
AGENDA
• Review of the current ADC landscape, both clinical and preclinical
Analyst
Beacon Targeted • Deep dive into the characteristics of ADCs in each stage of development
Therapies • Analyze trends on the recent flurry of ADC deals
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& Head of Research • Discover the development of a novel, catalytic payload class
Orum Therapeutics • Explore diversity of degrader SAR while also enabling conjugation
• Improve potency and selectivity of delivery to target cells
Stephen Slocum
Director of Drug
Development 3.00 Talk Reserved for LegoChem Biosciences
LegoChem
Biosciences
Maximizing Therapeutic Window to Increase Efficacy & Reduce Off-Target Toxicity of ADC
4.00 PEG-Based Bispecific ADC: Better Tumor Penetration, Wider Therapeutic
Shumin(Sam) Liu Window
Chief Executive Officer
Shenzhen Enduring • Assessing how it provides better tumor penetration
Biotech • Discussing how there were not any Fc related toxicities
• Exploring how it has a wider therapeutic window
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
strategy, drug-drug interaction risks
AGENDA
5.40 End of Conference
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East Asia has been very active in ADC research and
development; I am very interested to meet up other ADC
researchers and companies in Asia
Tse-Wen Chang, Founder Chairman, Immunwork
REGISTER YOUR PLACE
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
your offerings.
Top Three Reasons to Partner:
AGENDA
problem: they need a reliable up relationship building with Use this conference to ensure
service provider to help them key decision makers as well your services are key players in
with their ADC manufacturing as scientists that are using your the region.
needs. services daily.
Partner with us to ensure you are the company they think of when Asian-based drug developers outsourcing
ADC manufacturing. Get in touch today!
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15%
Asia
Director- 40%
North
America
President/Vice President- 5% Europe
Head/Manager- 15%
Professor- 10%
Scientist- 5%
GET INVOLVED
Rob Keast Matt Ashman
Partnerships Director Partnerships Director
Tel: +1 617 455 4188 Tel: +1 617 455 4188
Email: [email protected] Email: [email protected]
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
Abzena
Abzena is a life science group with headquarters in the UK, and chemistry and manufacturing
sites in the US. Abzena’s complimentary services and technologies in chemistry, biology
and manufacturing, are applied to the selection, development and manufacture of better
biopharmaceuticals. Abzena works with most of the top 20 biopharmaceutical companies
and academic groups all over the world and is focused on enabling the development of better
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treatments for patients. Abzena’s technologies have enabled many of its customers to progress
products through to clinical development. Abzena was created through the incorporation of
Antitope, PacificGMP, PolyTherics and The Chemistry Research Solution (TCRS); all of whom
now trade as Abzena.
www.abzena.com
BSP Pharmaceuticals
BSP Pharmaceuticals S.p. A. is focused on the development and manufacturing of anticancer
drugs with high potency and cytotoxitc characteristics for the Pharmaceuticals Industry. BSP has
been at the forefront in the fight against cancer since 2006. Innovation is the hallmark of BSP
with investments in new technologies and production methods in a high containment plant.
www.bsppharmaceuticals.com
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Thousand Oaks Biologics
Thousand Oaks Biologics (TOBio) is a leading CDMO specializing in the development and
manufacturing of biologics. TOBio offers CMC in antibody-drug conjugates, monoclonal
antibodies, and other recombinant protein products. The state-of-the-art GMP facilities at the
Shanghai ADC site include bioreactors, purification equipment, and fill-finish lines. TOBio’s
comprehensive quality management system ensures compliance with ICH, US FDA, EU EMA,
and China NMPA standards. With a proven track record of successful project delivery, including
over 100 clinical – stage projects and 3 pre-Approval inspections, TOBio is a trusted global
CDMO for biopharmaceutical companies.
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www.tobiopharm.com
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
WuXi XDC
WuXi XDC, a subsidiary of WuXi Biologics, is a leading global contract research, development
and manufacturing organization (CRDMO) focused on antibody drug conjugates (ADC) and the
broader bioconjugate market. The company’s end-to-end services cover antibody intermediates
and other biologics, chemical payloads and linkers, as well as bioconjugated drug substance
and drug product from concept to commercialization. WuXi XDC has been successful in bringing
multiple ADC projects to the Investigational New Drug (IND) filing stage in record time, nearly
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cutting in half the traditional development timeline.
www.wuxixdc.com
OminAb
OmniAb’s discovery platform provides pharmaceutical industry partners access to diverse
antibody repertoires and high-throughput screening technologies to enable discovery of next-
generation therapeutics. At the heart of the OmniAb platform is the Biological Intelligence™ (BI)
of our proprietary transgenic animals, including OmniRat®, OmniChicken® and OmniMouse®
that have been genetically modified to generate antibodies with human sequences to facilitate
development of human therapeutic candidates. OmniFlic® (transgenic rat) and OmniClic®
(transgenic chicken) address industry needs for bispecific antibody applications though a
common light chain approach, and OmniTaur™ features unique structural attributes of cow
antibodies for complex targets. We believe the OmniAb animals comprise the most diverse
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host systems available in the industry and they are optimally leveraged through computational
antigen design and immunization methods, paired with high-throughput single B cell phenotypic
screening and mining of next-generation sequencing datasets with custom algorithms to identify
fully human antibodies with superior performance and developability characteristics. These
proprietary technologies are joined with and leverage OmniDeep™, which is a suite of in silico
tools for therapeutic discovery and optimization that are woven throughout OmniAb’s various
technologies and capabilities. Additionally, an established core competency focused on ion
channels and transporters further differentiates OmniAb’s technology and creates opportunities
in many emerging target classes. OmniAb antibodies have been leveraged across modalities,
including bispecific antibodies, antibody-drug conjugates and others.
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The OmniAb suite of technologies span from BI-powered repertoire generation to cutting edge
antibody discovery and optimization offering a highly efficient and customizable end-to-end
solution for the growing discovery needs of the global pharmaceutical industry.
www.omniab.com
Samsung Biologics
Samsung Biologics is a fully integrated CDMO partner of choice, providing highly tailored
solutions to clients while meeting the evolving needs of the global healthcare industry. With
proven regulatory approvals, we provide seamless offerings from cell-line development to final
fill/finish at every stage for biopharmaceutical products. Our plants are cGMP compliant with a
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wide range of bioreactor scales to serve varying client needs and meet growing market demand.
We hold a total capacity of 604KL at Bio Campus I, the world’s largest biomanufacturing site,
and have announced plans to construct a fifth plant, which will be operational in 2025.
partner.samsungbiologics.com
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
Asymbio
AsymBio is the emerging business unit of Asymchem Group striving to become a
technology-driven, fully-empowered one-stop CDMO services platform for biologic (mAb,
ADC, plamsid&mRNA), offering customized services with outstanding quality and efficient
performance. We have built an integrated and comprehensive CDMO service platform for
ADC drugs (payload-linker, mAb, conjugation), which including but not limited to development,
manufacturing, quality control and regulatory affairs. Our one-stop ADC CDMO service platform
is able to efficiently empower ADCs.
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www.asymbio.com
Cytiva
Cytiva, now with the life sciences business from Pall Corporation, is a global biotechnology leader
dedicated to helping customers discover and commercialize the next generation of therapeutics.
We bring dedicated technical expertise and a broad portfolio of tools, technologies, and services
that enable the development, manufacture, and delivery of transformative medicines to patients.
www.cytivalifesciences.com/en/us
Aton Bio
Aton Biotech is a fast-growing CDMO company which is committed to enabling new biological
drugs for clients with an integrated bio-pharmaceutical platform. Our service ranges from cell line
development to clinical and end-to-end CDMO commercial manufacturing services, including
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development of mammalian expressed monoclonal antibodies, fusion proteins, bispecific
antibodies, ADC, etc.
www.atonbio.com
Axplora
Axplora, created from the merger of Farmabios, Novasep and PharmaZell, is a leading API
manufacturing partner to the world’s leading pharmaceutical and biotechnology companies,
delivering top quality active ingredients on time and at scale, to the highest industry standards.
Axplora is dedicated to helping pharmaceutical companies make critical medicines better, faster,
safely, reliably, and sustainably benefitting patients worldwide.
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The group provides unique services for the development, fast-track, clinical supply and
commercial cGMP manufacture of ADCs including the payload-linker and the bioconjugation,
leveraging its in-house purification expertise, HPAPI culture & state-of-the art cGMP conjugation
facilities. We offer a full and flexible range of ADC manufacturing services with hand-run
experience on different conjugation platforms.
www.axplora.com
PROVEO
Formed in 2015, PROVEO is now a Division of Cerbios- Pharma SA focused on complete
supply chain solution for Antibody Drug Conjugates (ADCs).
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Thanks to the partnership with AGC Biologics and Oncotec, PROVEO offer best-in-class
solutions for the integrated development and cGMP manufacturing of recombinant proteins (incl
mAbs), cytotoxic drug-linker payload, conjugation, aseptic fill and lyophilization. Strengths of
the three PROVEO partners secure a seamless and low risk ADC supply chain for clinical and
commercial projects.
www.proveoadc.com
ASIA 2024
WELCOME
June 25-27, 2024
Incheon, South Korea
EXPERT SPEAKERS
UK; a dedicated bioconjugation and ADCs facility in Deeside, North Wales, UK; and two sites in
the US, in Cary, North Carolina and Germantown, Wisconsin.
www.sterlingpharmasolutions.com
Levena
LEVENA is headquartered in Suzhou, China and has R&D centers and GMP manufacturing sites in
Nanjing and San Diego, with a total of about 20,000m2 of R&D and GMP manufacturing sites, covering
antibody, drug-linker, conjugation and lyophilization. Aimed to truly realize the one-stop service of
ADC. As a leading enterprise of Antibody-drug conjugate (ADC), LEVENA has been committed to the
development and industrialization of ADC. The company has the world’s leading new generation of site-
specific conjugation technology and a number of conjugate-related patents. At present, the company
has a mature and professional core technology platform, covering the research and development
and production of highly efficacious toxins (including Duostatins (Tubulin inhibitors), Duomycins (DNA
alkylating agents), and Camptothecins), and various site-specific conjugation methods (K-Lock,
C-Lock,C-Lock DXD and High DAR low toxicity platform). Based on this, it has carried out extensive
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cooperation with domestic and foreign pharmaceutical companies in the research and development
of new drugs. LEVENA’s patent platform has achieved all-round coverage from low toxicity high DAR
to high toxicity low DAR. Can meet the diverse needs of different requirements. At the same time,
based on the flexible application of platform technology, LEVENA can realize customized drug-linker
recommendation for specific projects and needs, help quickly and efficiently screen out the best pre-
clinical candidate ADC, and accelerate the whole project cycle.
www.levenabiopharma.com/cn/home
Levena
Henlius (2696.HK) is a global biopharmaceutical company with the vision to offer high-quality, affordable,
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and innovative biologic medicines for patients worldwide with a focus on oncology, autoimmune diseases,
and ophthalmic diseases. Up to date, 5 products have been launched in China, 2 have been approved for
marketing in overseas markets, 19 indications are approved worldwide, and 7 marketing applications have
been accepted for review in China, the U.S., and the EU, respectively. Since its inception in 2010, Henlius
has built an integrated biopharmaceutical platform with core capabilities of high-efficiency and innovation
embedded throughout the whole product life cycle including R&D, manufacturing and commercialization.
It has established global innovation centers and Shanghai-based manufacturing facilities in line with
global Good Manufacturing Practice (GMP), including Xuhui Facility and Songjiang First Plant, both
certificated by China and the EU GMP.Henlius has pro-actively built a diversified and high-quality product
pipeline covering over 50 molecules and has continued to explore immuno-oncology combination
therapies with proprietary HANSIZHUANG (anti-PD-1 mAb) as backbone. Apart from the launched
products HANLIKANG (rituximab), the first China-developed biosimilar, HANQUYOU (trastuzumab for
injection, trade name in Europe: Zercepac®), the first China-developed mAb biosimilar approved both
in China and Europe, HANDAYUAN (adalimumab) and HANBEITAI (bevacizumab), the innovative
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product HANSIZHUANG has been approved by the NMPA for the treatment of MSI-H solid tumours,
squamous non-small cell lung cancer (sqNSCLC) and extensive-stage small cell lung cancer (ES-SCLC),
and esophageal squamous cell carcinoma (ESCC), making it the world’s first anti-PD-1 mAb for the
first-line treatment of SCLC. What’s more, Henlius has conducted over 30 clinical studies for 16 products,
expanding its presence in major markets as well as emerging markets.
www.henlius.com/en/Index.html
WELCOME
biosimilars trend
Explore novel targets, linker
chemistries, payloads and more to
lead the charge in innovation
3 Easy Ways to Book
Navigate strategic collaborations
to improve global partnerships and
www.worldadc-asia.com/take-part/register increase communication with mega
pharma
Tel: +1 617 455 4188
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Email: [email protected]
Drug Developer Pricing Register & Pay by Friday, April 26 Final Price
Conference + Pre-Conference
$1,747 (Save $300) $2,047
Workshop Day
Conference Only $1,249 (Save $300) $1,549
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Solution Provider Pricing Register & Pay by Friday, April 26 Final Price
Conference + Pre-Conference
$4,597 (Save $300) $5,097
Workshop Day
Conference Only $3,399 (Save $300) $3,699
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Team Discounts** **Please note that discounts are only valid when three or more
delegates from one company book and pay at the same time.
• 10% discount – 3 Attendees Discounts cannot be used in conjunction with any other offer or
discount. Only one discount offer may be applied to the current
• 15% discount – 4 Attendees pricing rate.
Contact: [email protected]
• 20% discount – 5 + Attendees
Venue
Grand Hyatt Incheon
208 Yeongjonghaeannam-ro 321beon-gil, Jung-gu,
Incheon, South Korea
REGISTER YOUR PLACE
www.hyatt.com/en-US/hotel/south-korea/grand-hyatt-incheon/inche?