Study of people with Wilson disease genes and family members
Part of Brain & nervous system, Digestive system, Genetic & congenital, Hormones & metabolism clinical trials.
This study follows people who have the genetic cause of Wilson disease, including people who feel well and family members. Researchers want to better understand Wilson disease and what to watch for over time.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You must have a genetic diagnosis of Wilson’s disease, or be a relative/healthy comparison group
- You may be a Wilson’s disease carrier who has no symptoms
- If you are not a patient/carrier, you may qualify as a family member or an unrelated healthy control
- You (or your parent/legal guardian) must be willing and able to sign informed consent
- You must be able to follow study visits and instructions
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This trial is a patient registry that collects health information from people with Wilson’s disease, including those without symptoms yet and those taking any type of treatment. It helps researchers understand the disease and how it progresses, which can support future studies and care improvements.
This trial is testing an experimental gene therapy called PM577 that aims to fix the faulty gene causing Wilson disease. It might offer a new treatment option that could reduce or replace the need for daily medications.
This early-stage trial tests LY-M003, a new gene therapy treatment for Wilson's disease—a rare genetic condition where copper builds up in the body. The study aims to see if this injection is safe and whether it can help patients who are already on standard copper-lowering medicines.
This study measures how much copper is present in breast milk in people with Wilson’s disease. It aims to provide safer guidance for breastfeeding during treatment, including during pregnancy.
This trial tests an experimental mRNA treatment (DSL101) for adults with Wilson disease. It's for people whose condition is stable on current therapy and who have certain genetic markers. The goal is to see if the new treatment can help the body process copper better and reduce the need for standard medicines.
This study looks for early signs of heart problems in people with Wilson's disease. It uses imaging tests to check the heart, which may help catch issues early.
Hear when a new Wilson's Disease trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.