drugset / Trial / NCT01940341

Study to Compare Tenofovir Alafenamide (TAF) Versus Tenofovir Disoproxil Fumarate (TDF) in Participants With Chronic Hepatitis B Infection Who Are Negative for Hepatitis B e Antigen

NCT01940341 ↗

Phase 3 Completed 426 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to compare the efficacy, safety, and tolerability of tenofovir alafenamide (TAF) versus tenofovir disoproxil fumarate (TDF) in treatment-naive and treatment-experienced adults with hepatitis B e antigen (HBeAg)-negative chronic hepatitis B virus (HBV) infection.

Timeline

Start
2013-09-12
Primary completion
2015-09-30
Completion
2022-08-31

Outcome

Met primary endpoint

paper difference 1·8% [95% CI -3·6 to 7·2]; p=0·47), which demonstrates non-inferiority. PMID 28404092 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Subject tenofovir alafenamide Small molecule 25 mg Oral