drugset / Trial / NCT06680232

Phase 1 Study to Evaluate Safety and Antiviral Activity of PBGENE-HBV in Adult Patients With Chronic Hepatitis B

NCT06680232 ↗

Phase 1 Recruiting 45 enrolled Precision BioSciences, Inc.
NaSequentialOpen-labelTreatment

Summary

This is a Phase 1, open-label, dose escalation and dose expansion study to evaluate the safety, tolerability, PK, and antiviral activity of PBGENE-HBV in adult participants with chronic hepatitis B.

Timeline

Start
2024-11-14
Primary completion
2025-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject PBGENE-HBV Unknown — Intravenous