RecruitingPhase 3NCT06361537
Study of IV Human Plasma-derived C1 Esterase Inhibitor Concentrate in Patients With Congenital C1-INH Deficiency for Treatment and Pre-procedure Preventing of Acute Hereditary Angioedema Attacks
Studying Hereditary angioedema
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Octapharma
- Intervention
- OCTA-C1-INH(drug)
- Enrollment
- 124 enrolled
- Eligibility
- 2 years · All sexes
- Timeline
- 2024 – 2027
Study locations (19)
- Octapharma Research Site, Centennial, Colorado, United States
- Octapharma Research Site, Farmington Hills, Michigan, United States
- Octapharma Research Site, Toledo, Ohio, United States
- Octapharma Research Site, Tirana, Albania
- Octapharma Research Site, Rosario, Argentina
- Octapharma Research Site, Yerevan, Armenia
- Octapharma Research Site, Sofia, Bulgaria
- Octapharma Research Site, Lima, Mexico
- Octapharma Research Site, Mexico City, Mexico
- Octapharma Research Site, Podgorica, Montenegro
- Octapharma Research Site, Lima, Peru
- Octapharma Research Site, Cluj-Napoca, Romania
- Octapharma Research Site, Kragujevac, Serbia
- Octapharma Research Site, Ankara, Turkey (Türkiye)
- Octapharma Research Site, Istanbul, Turkey (Türkiye)
- +4 more locations on ClinicalTrials.gov
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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