Abstract 1
Abstract 1
Abstract 1
Renal Disease”, Sep, 2006, Toronto, Canada (Section 11, Abs 18, 2006)
Natarajan Ranganathan, Ph D1, Beena G Patel, Ph D1, Pari Ranganathan, MSMTASCP1, Rahul
Dheer, BS1, Richard Palmquist, DVM2 and Gary Van Engelenberg, DVM, CVA3. Eli A
Friedman, M.D.4 1
Kibow Biotech Inc, Newtown Square,, PA, United States; 2Centinela
Animal Hospital, Inglewood, CA, United States; 3Iowa Veterinary Acupuncture Clinic, C Des
Moines, IA, United States and 4 Downstate Medical Center, State University of New York
(SUNY), Brooklyn, NY, United States.
Azotemia declined during therapy; in cats (n=7), BUN fell from 54 13.0 to
45.1+12.0 mg/dl, while Scr decreased from 4.0 1.9 to 2.9 0.7 mg/dl.
Similar results were obtained in dogs (n=6), BUN decreased from 64.7 35.4
to 30.4 17.7 mg/dl, while Scr fell from 2.6 1.3 to 2.0 1.5 mg/dl. No adverse
effects were noted during 2-6 months of treatment. Survey questionnaires
sent to pet owners generated strongly positive results from the respondents,
who reported either significant improvement in uremia marker values or, in
more advanced cases of kidney failure, stabilization and improved quality of
life for their companion animals. These data are presented as a step in the
evolution of a gut-based uremia therapy with possible application in human
patients.
Our data support the view that testing efficacy of orally administered
probiotics in a clinical veterinary practice setting affords a rational
opportunity to confirm and validate inferences drawn from partially
nephrectomized test animals. A safety study in healthy volunteers has also
been accomplished with Kibow Biotics® (identical product formulation as
used in cats and dogs with renal failure) by our own group of volunteer
employees with required legal documentation. The next step is the initiation
of pilot scale human clinical trials in stage III and IV CKD patients. Efforts
are in progress towards accomplishing this goal in several countries.