drugset / Trial / NCT02174276

Safety and Efficacy of GS-4774 in Combination With Tenofovir Disoproxil Fumarate (TDF) for the Treatment of Participants With Chronic Hepatitis B (CHB) and Who Are Currently Not on Treatment

NCT02174276 ↗

Phase 2 Completed 195 enrolled Gilead Sciences
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objectives of this study are to evaluate the safety, tolerability, and efficacy of GS-4774 in adults with CHB and who are currently not on treatment. Participants will be randomized to receive TDF alone or GS-4774 plus TDF for 20 weeks. After Week 20, GS-4774 will be discontinued. All participants will continue on TDF and will be followed for an additional 28 weeks. Following completion of the 48 week study period, all participants will be eligible for a treatment extension for 96 weeks.

Timeline

Start
2014-07-24
Primary completion
2016-02-17
Completion
2018-05-30

Outcome

Missed primary endpoint

registry analysis (superiority test); TDF 48 Weeks vs TDF + GS-4774 2 YU; p = 0.805 NCT02174276 ↗

paper GS-4774 was safe and well tolerated but did not produce significant decreases in levels of HBsAg. PMID 30930022 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject GS-4774 Vaccine 2 unknown Subcutaneous
Subject GS-4774 Vaccine 10 unknown Subcutaneous
Subject GS-4774 Vaccine 40 unknown Subcutaneous
Background Tenofovir disoproxil fumarate Small molecule 300 mg Oral