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NCT Number: NCT07433621

Quercetin in Patients With XIAP (X-linked Inhibitor of Apoptosis) Deficiency

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.

Recruiting

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Key information

Age range

2 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

About this study

XIAP deficiency is a rare genetic immune disorder. XIAP usually suppresses inflammation and XIAP deficiency leads to increased inflammation. Patients may develop several inflammatory problems including hemophagocytic lymphohistiocytosis (HLH), a life-threatening syndrome of overwhelming inflammation characterized by fever, low blood counts (cytopenias), an enlarged spleen, liver problems, seizures, and other manifestations. Patients may develop milder symptoms such recurrent fevers or problems with low blood counts. Inflammatory bowel disease (IBD), arthritis or inflammation of the eyes (uveitis) can also occur, among other more rare complications. XIAP deficiency is often life-threatening and patients with severe disease require treatment with allogeneic hematopoietic cell transplantation (HCT), which is the only available curative treatment. Unfortunately, allogeneic HCT is associated with a high risk of mortality and significant side effects. Therefore, it's important to find other treatment options that are safe without major side effects.

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male patients
  • Diagnosis of XIAP deficiency
  • Patients ≥2 years of age
  • Serum IL-18 ≥600 pg/mL (approximately 25% above the lab-defined upper limit of normal of 477 pg/mL)
  • Able to take enteral medication

Exclusion criteria

  • Renal failure requiring dialysis
  • Total bilirubin >3 mg/dl and/or SGPT >300 at time of enrollment
  • Patients receiving digoxin therapy, who are unable to discontinue treatment due to medical reasons
  • Patients receiving fluoroquinolone therapy, who are unable to discontinue treatment due to medical reasons
  • Patients who are at risk of pregnancy or fathering a child and are unable to use acceptable methods of birth control during the length of the study
  • Patients who have received quercetin or any over the counter anti-oxidant supplementation within last 1 month
  • Patients with unstable disease status or other medical issues requiring hospitalization or rapid escalation of medical care
  • Participating in another therapeutic study for XIAP deficiency

Treatment and study plan

Quercetin

Drug

Quercetin 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.

Primary outcomes

  1. Safety of quercetin in patients with XIAP deficiency

    Time frame: 6 months

    Assessment of AEs

  2. Tolerability of quercetin in patients with XIAP deficiency

    Time frame: 6 months

    Number of subjects who discontinue study drug due to intolerance

Secondary outcomes

  1. Pharmacokinetics (PK) of quercetin in patients with XIAP deficiency

    Time frame: Pre and post dose at baseline, 2 months, and 6 months

    'Area under the curve (AUC)' will be utilized to describe PK of quercetin in these patients

Study contacts

Contact information is provided by the study sponsor or research team.

Kelly McIntosh

CONTACT

[email protected]

513-803-0460

Richard Cooper

CONTACT

[email protected]

513-803-7450

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Registry information

Official study title

A Pilot Study to Evaluate Safety and Tolerability, Pharmacokinetics, and Preliminary Efficacy of Quercetin in Patients With XIAP (X-linked Inhibitor of Apoptosis) Deficiency

Important dates

Study start
2026
Primary completion
2028
Study completion
2029
First posted
Feb 25, 2026
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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