drugset / Trial / NCT03365947

Study of ARO-HBV in Normal Adult Volunteers and Patients With Hepatitis B Virus (HBV)

NCT03365947

Phase 1/2 Completed 114 enrolled Arrowhead Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single- and multiple-ascending doses of ARO-HBV in healthy adult volunteers and participants with hepatitis B virus (HBV).

Timeline

Start
2018-03-27
Primary completion
2020-04-23
Completion
2020-04-23

Drugs

EvaluationDrugModalityDoseRoute
Subject ARO-HBV Unknown 25 mg Subcutaneous
Subject ARO-HBV Unknown 35 mg Subcutaneous
Subject ARO-HBV Unknown 50 mg Subcutaneous
Subject ARO-HBV Unknown 100 mg Subcutaneous
Subject ARO-HBV Unknown 200 mg Subcutaneous
Subject ARO-HBV Unknown 300 mg Subcutaneous
Subject ARO-HBV Unknown 400 mg Subcutaneous
Subject bersacapavir Other / unclassified 250 mg