Rare Disease Trial, Recruiting
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:
- Children or adults who are suspected of having a rare disease (or a rare form of a common disease) that is thought to be genetic, but where the genetic cause or how the disease works is not yet fully understood
- Unborn babies (foetuses) who have developmental abnormalities where the genetic cause or how the condition works is not yet fully understood
- Family members who appear to be healthy, or people participating as comparison (control) participants
- The patient, or their legal guardian if the patient cannot consent for themselves, must agree to take part
- The patient or their guardian must have a suitable level of understanding to participate
Who may not be able to join:
- People who do not have national health insurance coverage
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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Number of new genes or genetic abnormalities identified.
Can't join this trial?
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.