Hepatitis B Trial, Recruiting NCT06047093 Sponsor: Hospices Civils de Lyon Condition: Hepatitis B
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Hepatitis B Trial, Recruiting

NCT06047093
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
  • People who have a long-term (chronic) hepatitis B virus infection, at any stage
  • People who are currently taking antiviral medication for hepatitis B (called nucleoside analogues), or those who are not on any treatment
  • People who also have a hepatitis D virus (HDV) infection, or those who do not
  • People who are already enrolled in a separate related study called the CirB-RNA study (NCT03825458)
  • People who have been fully informed about the study and have signed a consent form

Who may not be able to join:

  • Women who are pregnant, in labour, or currently breastfeeding
  • People whose liver disease has become severely advanced (decompensated cirrhosis)
  • People who have liver cancer, or where liver cancer is suspected
  • People who have had a liver transplant, even if the transplant was due to hepatitis B
  • People who also have an active hepatitis C infection or an HIV infection
  • People who are currently taking part in another clinical trial that involves a treatment or intervention
  • People who are under psychiatric care
  • People who are living in a health or social care facility for reasons unrelated to research
  • Adults who are under a legal protection order (such as guardianship or curatorship)
  • People who are not covered by a social security or equivalent health insurance scheme
  • People who have skin problems or infections on their abdomen (stomach area)
  • People who have an allergy or sensitivity to lidocaine (a local anaesthetic used in the study)

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: Fabien ZOULIM, PU-PH, Service d'Hépatologie de l'Hopital Croix-Rousse

Phone: 0426109355

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
Registry
ClinicalTrials.gov
Start date
8 March 2024
Est. completion
8 March 2030

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Interaction between immune response against HBV and intrahepatic HBV viral load

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