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 项与 Elim Pediatric Pharmaceuticals Inc. 相关的临床结果
0 项与 Elim Pediatric Pharmaceuticals Inc. 相关的专利(医药)
100 项与 Elim Pediatric Pharmaceuticals Inc. 相关的药物交易
100 项与 Elim Pediatric Pharmaceuticals Inc. 相关的转化医学