Fact CheckerSign in

NCT06680232RecruitingPhase 1

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

A Phase 1, Open-Label, First-in-Human, Dose Escalation (Part 1) and Expansion (Part 2) Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of PBGENE-HBV in Participants With Chronic Hepatitis B (ELIMINATE-B)

Source: ClinicalTrials.gov · Last updated 24 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
45 (estimated)
First submitted
24 Oct 2024
Start date
14 Nov 2024
Primary completion date
Dec 2026
Lead sponsor
Precision BioSciences, Inc.
Diseases
Hepatitis B
NCT number
NCT06680232
EU CT number
2025-524157-13-00

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 45
  • From 14 Nov 2024 to the primary completion date, Dec 2026
  • 7 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Not received an organ transplant
  • No investigational agent received within 6 months of screening

Other illness

  • No history of cirrhosis of the liver
  • No current infections of Hepatitis A, D, and E, human immunodeficiency virus (type 1 and 2), and no history of or current hepatitis C. In addition, no other active infections deemed clinically relevant.
  • No malignancy within 5 years of screening, except for specific cancers that are cured by surgical resection (e.g., basal cell skin cancer)

Other

  • No signs of hepatocellular carcinoma

Who the study is looking for

  • Male or women of non-child bearing potential
  • BMI 18.0 to 35.0
  • Good overall health deemed by the study Investigator
  • CHB infection documented at least 12 months prior to screening
  • HBeAg-negative CHB
  • Must be virologically suppressed on current NA treatment

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (7)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Beaujon
Coordinator of this site? Confirm its status
ClichyFranceRecruiting
Queen Mary Hospital, The University of Hong Kong
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaRecruiting
ICS ARENSIA Exploratory Medicine SRL
Coordinator of this site? Confirm its status
ChisinauMoldovaRecruiting
New Zealand Clinical Research
Coordinator of this site? Confirm its status
AucklandNew ZealandRecruiting
National Institute of Infectious Diseases Prof. Dr. Matei Bal
Coordinator of this site? Confirm its status
BucharestRomaniaRecruiting
County Clinical Emergency Hospital Cluj-Napoca
Coordinator of this site? Confirm its status
Cluj-NapocaRomaniaRecruiting
Massachusetts General Hospital-Harvard University
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.