Active, not recruitingPhase 3NCT04747613
Long-term Safety and Tolerability of Iptacopan in Patients With Paroxysmal Nocturnal Hemoglobinuria
Studying Paroxysmal nocturnal hemoglobinuria
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
- Novartis Pharmaceuticals
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- Iptacopan(drug)
- Enrollment
- 208 enrolled
- Eligibility
- 18-100 years · All sexes
- Timeline
- 2021 – 2027
Study locations (30)
- City Of Hope, Duarte, California, United States
- USC Norris Cancer Center, Los Angeles, California, United States
- Univ of California Irvine (Chao Family Comprehensive Cancer Center), Orange, California, United States
- Lakes Research, Miami Lakes, Florida, United States
- Augusta University, Augusta, Georgia, United States
- Montefiore Medical Center, The Bronx, New York, United States
- Cleveland Clinic Foundation, Cleveland, Ohio, United States
- Prisma Health Upstate, Greenville, South Carolina, United States
- Novartis Investigative Site, Santo André, São Paulo, Brazil
- Novartis Investigative Site, São Paulo, São Paulo, Brazil
- Novartis Investigative Site, Beijing, China
- Novartis Investigative Site, Tianjin, China
- Novartis Investigative Site, Ostrava, Poruba, Czechia
- Novartis Investigative Site, Brno-Bohunice, Czechia
- Novartis Investigative Site, Lille, France
- +15 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.
Open NCT04747613 on ClinicalTrials.govOther trials for Paroxysmal nocturnal hemoglobinuria
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