The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.
Verified·NCT04537377Synced: Oct 28, 2026Active, not recruitingPHASE1/PHASE2

A Phase I/II Study of VTX-801 in Adult Patients With Wilson's Disease

Plain-language summary

This study examines a gene therapy called VTX-801 in adult patients with Wilson's disease. It enrolls patients aged 18 to 65 with a confirmed diagnosis of Wilson's disease whose condition has been stable for at least one year. The study is in Phase 1/Phase 2; it is currently not recruiting participants but is still ongoing (active, not recruiting).

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase
PHASE1/PHASE2
Status
Active, not recruiting
Sponsor
Vivet Therapeutics SAS
Intervention
VTX-801
Start date
9/3/2021
Estimated completion
6/18/2029
Countries
United States, Denmark, Germany, United Kingdom

Related genes

Locations

  • Sacramento, United States
  • New Haven, United States
  • Orlando, United States
  • Ann Arbor, United States
  • Winston-Salem, United States
  • Dallas, United States
  • Aarhus, Denmark
  • Essen, Germany
  • Tübingen, Germany
  • Guildford, United Kingdom

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

Main Inclusion Criteria:

* Male or female aged 18 and 65 years inclusive
* Confirmed diagnosis of WD
* Treated for WD according to international recommendations with no current evidence for inadequate treatment
* Stable WD for ≥ 1 year, defined as: (i) No significant change in neurologic examination and in status of mood disorder and (ii) Stable laboratory parameters used to assess copper metabolism

Main Exclusion Criteria:

* ALT level ≥ 2 ULN that is not readily explained by extrinsic factors
* Total bilirubin \> 1.5 x ULN in the absence of proven Gilbert's syndrome; in case of Gilbert's syndrome, direct bilirubin \> ULN
* INR \> 1.2
* Any signs of liver cirrhosis decompensation, including gastrointestinal bleed within 6 months (24 weeks) prior to screening/enrollment visit
* Patient has moderate or severe renal impairment defined as eGFR CKD-EPI \< 60 mL/min/1.73 m2, or patient has nephritis or nephrotic syndrome
* Any history or current evidence of HIV-1, HIV-2, HTLV 1, or HTLV-2 infection
* Any history or current evidence of hepatitis B infection
* Any history of hepatitis C infection, unless previous viral RNA assays in two samples, collected at least 6 months apart, are negative
* Positive QuantiFERON®-TB Gold tuberculosis test result
* Any concomitant disorder/condition - including hepatic disorders - or treatment possibly interfering with the conduct or evaluation of the study
* Any history of diabetes
* Pregnancy or breastfeeding
* Body Mass Index ≥ 35 kg/m2

Other protocol defined Inclusion/ Exclusion criteria may apply
This is not medical advice. Consult your specialist.
View the official record on ClinicalTrials.gov →