Hepatitis C Trial, Recruiting NCT05653232 Sponsor: Johns Hopkins University Condition: Hepatitis C
Back to Hepatitis C

Hepatitis C Trial, Recruiting

NCT05653232
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:

  • People who meet the standard requirements for a kidney transplant at the participating hospital or centre.
  • People who are able to understand the study information and agree to take part by giving informed consent.
  • People who are 18 years of age or older.

Who may not be able to join:

  • People who have an active hepatitis C virus (HCV) infection that is detectable in their blood at the time of screening.
  • People who have cirrhosis (severe liver scarring) or advanced liver fibrosis (significant liver scarring).
  • People whose liver enzyme levels (specific blood markers called AST or ALT) are more than 2.5 times higher than the normal upper limit, based on a blood test taken within the 60 days before screening.
  • People who have HIV (human immunodeficiency virus) infection, or an active hepatitis B (HBV) infection.
  • People who are taking a medication that cannot be safely stopped or swapped out, if that medication is known to interact badly with the study drug.
  • People who have past or current health conditions that could increase the risks of being in the study, make it difficult to follow the study requirements, or affect the reliability of the study results (confirm with trial site).
  • People who are currently pregnant or breastfeeding.

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 28 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: Christine Durand, MD, Johns Hopkins University

Phone: 410-955-5684

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
19 April 2023
Est. completion
1 September 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Composite event of HCV-related or HCV treatment-related death, fibrosing cholestatic hepatitis, or HCV relapse; Number of participants with liver injury

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: 28 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