Active, not recruitingPhase 4NCT07076446
An Open-label, Multicenter Study to Assess the Pharmacokinetics (PK), Safety, and Tolerability of Subcutaneous IgPro20 in Immunoglobulin (IG) Treatment-naïve Participants With Primary Immunodeficiency (PID)
Studying Primary immunodeficiency
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CSL Behring
- Principal Investigator
- Study DirectorCSL Behring
- Intervention
- IgPro(biological)
- Enrollment
- 8 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2026
Study locations (8)
- Research Solutions of AZ, Litchfield Park, Arizona, United States
- Medical Research of Arizona, Scottsdale, Arizona, United States
- Immunoe Health Centers, Centennial, Colorado, United States
- Johns Hopkins Bayview Medical Center, Baltimore, Maryland, United States
- Midwest Immunology, Plymouth, Minnesota, United States
- Washington University, St Louis, Missouri, United States
- Allergy, Asthma and Clinical Research Center, Oklahoma City, Oklahoma, United States
- Allergy & Clinical Immunology, Pittsburgh, Pennsylvania, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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