drugset / Trial / NCT07024641

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of GIGA-2339 in Participants With Chronic Hepatitis B Virus Infection

NCT07024641 ↗

Phase 1 Recruiting 48 enrolled GigaGen, Inc.
RandomizedSequentialDouble-blindTreatment

Summary

The primary purpose of this study is to assess the safety and tolerability of single and multiple intravenous (IV) doses of GIGA-2339 in participants with chronic Hepatitis B Virus (HBV) infection.

Timeline

Start
2024-11-13
Primary completion
2028-11
Completion
2028-11

Drugs

EvaluationDrugModalityDoseRoute
Subject GIGA-2339 Unknown — Intravenous