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
Delaware
Dover
District of Columbia
Washington D.C.
Florida
Tallahassee
Georgia
Atlanta
Idaho
Boise
Illinois
Springfield
Source: ClinicalTrials.gov · NCT06605378 · last updated 2026-08-17