Quercetin in Patients With XIAP (X-linked Inhibitor of Apoptosis) Deficiency
Part of paid clinical trials in Cincinnati, Ohio.
- Sponsor
- Children's Hospital Medical Center, Cincinnati
- Study ID
- NCT07433621
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- XIAP Deficiency
Eligibility Criteria
- Sex
- MALE
- Age
- 2 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Quercetin — DRUGQuercetin will be administered orally at a weight adjusted dose for a maximum total daily dose of 4000mg/day, divided twice a day. If the patient is 70 kg or more, the dose will automatically be assigned at the maximum dose of 4000mg/day. Patients will be instructed to mix quercetin with a small amount of yogurt or other preferred food for ingestion.
Study Details
The purpose of the study is to evaluate safety and tolerability of oral quercetin in reducing inflammation in male patients with XIAP deficiency. Quercetin is a naturally occurring antioxidant that has many properties including the ability to decrease inflammation in other diseases.
Key Dates
- Start date
- Feb 26, 2026
- Status verified
- Mar 2026
- Primary completion
- Nov 30, 2028
- Completion
- Jun 30, 2029
Study Design
- Enrollment
- 12 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: QuercetinAll subjects will receive a weight adjusted dose of quercetin for a maximum total daily dose of 4000mg/day, divided twice a day.
Primary Outcome Measure
Safety of quercetin in patients with XIAP deficiency [ Time Frame: 6 months ]
Central Contacts
- Kelly McIntosh513-803-0460
- Richard Cooper513-803-7450
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Cincinnati Children's Hospital Medical Center | Cincinnati | Ohio | 45229 | Rebecca Marsh, MD (PRINCIPAL_INVESTIGATOR) |
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