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Not recruiting

Observational Study

Sponsor:

Prime Medicine, Inc.

Code:

NCT07226622

Conditions

Wilson Disease

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

The aim of this study is to inform and improve future clinical trials in Wilson Disease (WD) by better understanding how patients with WD are living with and managing the disease, and by identifying key factors that shape their decisions to participate in clinical research.

Conditions

Wilson Disease

Study ID

NCT07226622

Start date

Dec 29, 2025

Status verified date

Oct, 2025

Completion date

Dec, 2027

Anticipated

Primary completion date

Dec, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Confirmed Wilson Disease (WD) as determined by the following criteria:

1. An established clinical diagnosis of WD
2. Genetic analysis confirming the presence of biallelic pathogenic variants at ATP7B, at least one of which is EITHER p.H1069Q OR p.R778L OR Participants without a confirmed genetic diagnosis may enroll only with explicit approval from the Medical Monitor

Exclusion Criteria:

1. Prior history of gene therapy, liver transplantation, hepatocyte (cellular) transplantation, or active listing for liver transplantation
2. For individuals with known ATP7B genotype: individual does not have at least 1 ATP7B allele with either the p.H1069Q or p.R778L mutation.
3. Significant neurological conditions within the prior 12 months which may impact participant safety or participation in the study, including ability to complete study requirements or procedures as outlined in the clinical study protocol.
4. In patients with psychiatric involvement, current or fluctuant clinical instability with new or changing diagnoses or substantial medication regimen changes in the past 12 months that could limit their participation, in the opinion of the Investigator.
5. History of cirrhotic decompensation within the past year.
6. Any other condition that, in the opinion of the Investigator, may compromise the safety or compliance of the participant or would preclude the participant from successful study completion, including participant unable or unwilling to comply with the protocol requirements.
7. Current participation in an investigational study for the treatment of WD.
8. Prior or active malignancy or myeloproliferative disorder (excluding Stage 1 or lower, fully treated/excised malignant and pre-malignant disease of the skin, cervix or colon. Additionally, any other malignant and pre-malignant disease that the Investigator in consultation with the treating oncologist and study Medical Monitor deem has been fully treated/excised for > 5 years).

Study Design

Enrollment

30 participants

Anticipated

Interventions and Outcome Measures

Arms

Participants with at least 1 allele with the ATP7B p.H1069Q or p.R778L mutation

Primary outcome measure

  • Gene Editing Interest & Attitudes Survey [ Time Frame: From enrollment to the end of study 90 days ]

Central Contacts and Locations

More Information

Sponsor

Prime Medicine, Inc.

Last update posted

May 12, 2026

Last verified

Oct, 2025

Keywords

  • Hepatolenticular Degeneration
  • Liver Diseases
  • Genetic Diseases, Inborn
  • Congenital, Hereditary, and Neonatal Diseases and Abnormalities
  • Metabolism, Inborn Errors
  • Metal Metabolism, Inborn Errors
  • Metabolic Diseases
  • Nutritional and Metabolic Diseases

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-17. This information was provided to ClinicalTrials.gov by Prime Medicine, Inc. on 2026-05-12. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.