Hepatitis B Trial, Recruiting NCT06853886 Sponsor: University Hospital, Limoges Condition: Hepatitis B
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Hepatitis B Trial, Recruiting

NCT06853886
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older who have a hepatitis B virus (HBV) infection, whether it is untreated or being treated with a certain type of antiviral medication
  • People who are willing and able to sign a written consent form agreeing to take part
  • People who are covered by a social security scheme
  • Healthy volunteers aged between 18 and 80 who are willing and able to sign a written consent form agreeing to take part

Who may not be able to join:

  • People who also have a hepatitis C (HCV), HIV, or hepatitis D (HDV) infection — and for healthy volunteers, this also includes having hepatitis B (HBV)
  • People who had an episode of acute (sudden onset) hepatitis in the year before joining the trial
  • People with other liver-related conditions, such as those linked to heavy alcohol use, obesity (body mass index over 30), diabetes, or a combination of high cholesterol/fats and known high blood pressure
  • People with an underlying immune system disorder or a cancer diagnosis
  • People whose condition prevents them from fully understanding what taking part in the trial involves
  • People who are under court protection, legal guardianship, or a similar legal arrangement
  • Women who are pregnant or breastfeeding
  • Healthy volunteers whose vaccination records do not match what would be expected based on their blood test results (confirm with trial site)
  • Anyone whose blood pregnancy test comes back positive at the time of joining
  • Patients who test positive for HCV, HIV, or HDV at the time of joining
  • Healthy volunteers who test positive for HBV, HCV, HIV, or HDV at the time of joining

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Paul CARRIER, MD, University Hospital, Limoges

Phone: +335 55 05 80 22

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University Hospital, Limoges
Registry
ClinicalTrials.gov
Start date
12 August 2025
Est. completion
1 October 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

RNA sequencing of B cells from CHB patients at different stages, description of their molecular signature

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov