Phase I Three-way Crossover Bioequivalence Study of Pediatric Formulations of Lamivudine/Zidovudine/Nevirapine Using Healthy Adult Volunteers
The purpose of the study is to determine the bioavailability/bioequivalence of two pediatric formulations (tablet and reconstitutable suspension) of lamivudine/zidovudine/ nevirapine in comparison to an innovator product. Establishing the bioequivalence of a newly developed age-appropriate fixed dose combination of lamivudine/zidovudine/ nevirapine as an oral dispersible tablet or a reconstitutable suspension for children is invaluable for future product registration and availability of the products to children, thus filling the void in pediatric HIV/AIDS therapy.
100 Clinical Results associated with Elim Pediatric Pharmaceuticals Inc.
0 Patents (Medical) associated with Elim Pediatric Pharmaceuticals Inc.
100 Deals associated with Elim Pediatric Pharmaceuticals Inc.
100 Translational Medicine associated with Elim Pediatric Pharmaceuticals Inc.