A Long-term Observational Study in Participants Who Have Received PBGENE-HBV
Conditions:
Chronic HBV Infection
Sponsor: Precision BioSciences, Inc.
trial.available_in:
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Overview
Participants who received at least one dose of PBGENE-HBV will be enrolled in this LTFU study.
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.
Who can participate
Inclusion Criteria:
1. Participant has received at least 1 dose of PBGENE-HBV investigational product in a prior clinical study
2. Participant, or their legally authorized representative, has provided signed informed consent.
Exclusion Criteria:
* N/A
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