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

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Precision BioSciences, Inc.
Study ID
NCT07254208
Status
Enrolling By Invitation

Conditions

  • Chronic HBV Infection

Eligibility Criteria

Sex
ALL
Age
19 Years - 80 Years
Healthy Volunteers
Not accepted

Interventions

  • PBGENE-HBV — BIOLOGICAL
    PBGENE-HBV is the investigational product administered in the parent study. This LTFU study is non-interventional; no investigational product given.

Study Details

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

Key Dates

Start date
Dec 25, 2025
Status verified
Apr 2026
Primary completion
Jan 31, 2040
Completion
Jun 30, 2040

Study Design

Enrollment
45 participants (estimated)

Primary Outcome Measure

Safety to assess frequency, severity, and outcome of delayed adverse events [ Time Frame: 15 years ]

Locations (1)

FacilityCityStateZIPSite coordinators
Massachusetts General Hospital/Harvard UniversityBostonMassachusetts02114-

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