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:
- You have a known or suspected change (variant) in a gene called RUNX1
- You have symptoms that suggest a condition called Familial Platelet Disorder (FPD), even if you have not been tested for RUNX1 yet
- You were previously tested for RUNX1 but the result came back negative, yet you still have symptoms that raise suspicion of this condition
- You are a family member (without symptoms) who may be asked to provide samples such as saliva, blood, or skin for genetic testing
- You can be any age — there is no minimum or maximum age requirement
- You can be any sex
Who may not be able to join:
- There are no stated exclusion criteria for this trial — no groups of people are specifically ruled out
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.
Contact this trial
Principal Investigator: Paul Liu, M.D., National Human Genome Research Institute (NHGRI)
Phone: (301) 385-5205
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
Where this trial is recruiting
Primary endpoints
Natural History
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.