RecruitingPhase 3NCT05935215
Efficacy and Safety of Switching From Anti-C5 Antibody Treatment to Iptacopan Treatment in Study Participants With Atypical Hemolytic Uremic Syndrome (aHUS)
Studying Atypical hemolytic uremic syndrome
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
- 50 enrolled
- Eligibility
- 18-100 years · All sexes
- Timeline
- 2024 – 2029
Study locations (29)
- Novartis Investigative Site, Nanjing, Jiangsu, China
- Novartis Investigative Site, Beijing, China
- Novartis Investigative Site, Shanghai, China
- Novartis Investigative Site, Bordeaux, France
- Novartis Investigative Site, Paris, France
- Novartis Investigative Site, Rouen, France
- Novartis Investigative Site, Toulouse, France
- Novartis Investigative Site, Tours, France
- Novartis Investigative Site, Essen, Germany
- Novartis Investigative Site, Kiel, Germany
- Novartis Investigative Site, Ranica, BG, Italy
- Novartis Investigative Site, Milan, MI, Italy
- Novartis Investigative Site, Roma, RM, Italy
- Novartis Investigative Site, Matsumoto-shi, Nagano, Japan
- Novartis Investigative Site, Iruma-gun, Saitama, Japan
- +14 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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