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Not Yet RecruitingNCT07254208

A Long-term Observational Study in Participants Who Have Received PBGENE-HBV

A Long-term Observational Study in Participants Who Have Received PBGENE-HBV, an In Vivo Gene Editing Investigational Product, in a Prior Clinical Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
45 (estimated)
Sponsor
Precision BioSciences, Inc. · Industry
Sex
All
Age
19 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Participants who received at least one dose of PBGENE-HBV will be enrolled in this LTFU study.

Detailed description

This is a LTFU observational study designed to evaluate the safety of PBGENE-HBV in participants previously exposed to PBGENE-HBV. This study protocol does not include administration of PBGENE-HBV.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPBGENE-HBVPBGENE-HBV is the investigational product administered in the parent study. This LTFU study is non-interventional; no investigational product given.

Timeline

Start date
2025-12-25
Primary completion
2040-01-01
Completion
2040-06-01
First posted
2025-11-28
Last updated
2025-11-28

Regulatory

Source: ClinicalTrials.gov record NCT07254208. Inclusion in this directory is not an endorsement.

A Long-term Observational Study in Participants Who Have Received PBGENE-HBV (NCT07254208) · Clinical Trials Directory