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Whole Blood Biospecimen Collection for Subjects With Chronic Granulomatous Disease (CGD)

S

Sanguine Biosciences

Status

Terminated

Conditions

Chronic Granulomatous Disease

Treatments

Diagnostic Test: Specimen Donation

Study type

Observational

Funder types

Industry

Identifiers

NCT05915897
SAN-09687

Details and patient eligibility

About

The primary study objective is to collect biospecimen samples (e.g., blood) from participants diagnosed with Chronic Granulomatous Disease (CGD). The biospecimens will be used to create a biorepository that can be used to identify disease associated biomarkers and potential targets with immune and multi-omics profiling. The disease sample collection and analysis will be the foundation for an extensive network of biospecimen access and linked datasets for future translational research.

Enrollment

6 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The participant is willing and able to provide written informed consent
  • The participant is willing and able to provide appropriate photo identification
  • Participants aged 18 to 85
  • Participants have been diagnosed with Chronic Granulomatous Disease (CGD)
  • Subjects who have a confirmed p47phox CGD mutation or Subjects who have a confirmed X-linked CGD mutation

Exclusion criteria

  • Participants who are pregnant or are nursing
  • Participants with a known history of HIV, hepatitis, or other infectious diseases
  • Participants who have taken an investigational product in the last 30 days
  • Participants who have experienced excess blood loss, including blood donation, defined as 250 mL in the last month or 500 mL in the previous two months

Trial design

6 participants in 2 patient groups

CGD with p47phox phenotype
Treatment:
Diagnostic Test: Specimen Donation
X-Linked CGD
Treatment:
Diagnostic Test: Specimen Donation

Trial contacts and locations

1

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Central trial contact

Taylor Caccia

Data sourced from clinicaltrials.gov

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