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RecruitingChronic Granulomatous Disease (CGD)

Prevalence of Antibodies and Cytokines in Participants With Chronic Granulomatous Disease

Eligible age

All ages

Accepts

All genders

Locations

49 states

Healthy volunteers

No

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About this study

This research study is designed to assess the prevalence of specific antibodies and inflammatory cytokines in adult and pediatric participants with CGD.

Sponsor: Ensoma

You may qualify if…

  • The participant must have been diagnosed with CGD based on the referring physician's confirmation that NADPH oxidase activity is ≤5% (i.e., the percentage of dihydrorhodamine-positive \[DHR+\] cells is ≤5% by flow cytometry) OR based on confirmed pathogenic mutation in a CGD associated gene (CYBB, CYBA, NCF1, NCF2, NCF4, or CYBC1).
  • The participant or the participant's legally authorized guardian or representative (if applicable) must be capable of giving signed informed consent.
  • The participant (with assistance from the participant's legally authorized guardian/representative or primary caregiver, if applicable) must be capable of complying with the requirements and restrictions listed in the protocol and informed consent form (ICF).

You may not qualify if…

  • The participant has undergone an allogeneic bone marrow transplant or investigational gene therapy.
  • The participant is unable to comply with the sample collection procedure based on investigator judgment.

Where it's recruiting

Alabama

Montgomery

Arizona

Phoenix

Arkansas

Little Rock

California

Sacramento · San Francisco

Colorado

Denver

Connecticut

Hartford

District of Columbia

Washington D.C.

Florida

Tallahassee

Georgia

Atlanta

Idaho

Boise

Illinois

Springfield

Source: ClinicalTrials.gov · NCT06605378 · last updated 2026-08-17