drugset / Trial / NCT02288208

Phase I Safety and Tolerability Study of Birinapant in Chronic Hepatitis B

NCT02288208

Phase 1 Terminated 7 enrolled TetraLogic Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

This study evaluates the addition of birinapant in subjects with chronic Hepatitis B who are currently receiving anti-viral therapy with either tenofovir or entecavir. Patients will receive either birinapant or placebo in addition to their anti-viral therapy.

Timeline

Start
2014-11
Primary completion
2015-05
Completion
2015-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Birinapant Small molecule Intravenous
Background Entecavir Small molecule 0.5 mg Oral
Background Tenofovir Small molecule 300 mg Oral