Clinical Trial

Bioequivalence Study of Tenofovir Disoproxil Fumarate Tablets in Healthy Chinese Subjects

Completed Phase 1
View on ClinicalTrials.gov →
Summary
This study evaluated the bioequivalence and safety of the test formulation (Tenofovir Disoproxil Fumarate Tablets, Haisco Pharmaceutical Group Co., Ltd.) and the reference formulation (Viread®, Gilead Sciences, Inc.) in healthy Chinese subjects under fasting and fed conditions
Trial Details
NCT Number NCT07558967
Lead Sponsor Haisco Pharmaceutical Group Co., Ltd.
Conditions Healthy
Enrollment 47 participants
Start Date 2017-06-20
Primary Completion 2017-08-23 (estimated)
Study Completion 2017-11-20 (estimated)
Updated on ClinicalTrials.gov 2026-04-30