Whole Blood Biospecimen Collection for Subjects With Chronic Granulomatous Disease (CGD)
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Chronic Granulomatous Disease
- Sponsor
- Sanguine Biosciences
- Enrollment
- 6
- Locations
- 1
- Primary Endpoint
- Participants have been diagnosed with Chronic Granulomatous Disease (CGD)
- Status
- Terminated
- Last Updated
- 2 years ago
Overview
Brief Summary
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.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Participants have been diagnosed with Chronic Granulomatous Disease (CGD)
Time Frame: 1 Year
Participants have been diagnosed with Chronic Granulomatous Disease (CGD)