Active, not recruitingPHASE1, PHASE2NCT03157635
Study to Assess Safety, Efficacy, Pharmacokinetics, and Pharmacodynamics of Crovalimab in Healthy Volunteers and Participants 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
- Hoffmann-La Roche
- Principal Investigator
- Clinical TrialsHoffmann-La Roche
- Intervention
- Crovalimab(drug)
- Enrollment
- 59 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2016 – 2026
Study locations (14)
- Institut hematologie Centre Hayem CHU paris Saint-Louis Lariboisiere F Widal Hopital St Louis, Paris, France
- Uniklinik RWTH Aachen, Aachen, Germany
- Universitätsklinikum Essen, Essen, Germany
- Universitätsklinikum Ulm, Ulm, Germany
- Semmelweis Egyetem, 1. Szamu Belgyogyaszati Klinika, Diabetologia, Budapest, Hungary
- Kaposi Mor Teaching Hospital, Dept of Internal Medicine/Hematology, Kaposvár, Hungary
- Policlinico Universitario Agostino Gemelli, Rome, Lazio, Italy
- Tohoku University Hospital, Miyagi, Japan
- Osaka University Hospital, Osaka, Japan
- NTT Medical Center Tokyo, Tokyo, Japan
- Tokyo Medical University Hospital, Tokyo, Japan
- University of Tsukuba Hospital, Tsukuba, Japan
- Pra International Group B.V, Groningen, Netherlands
- Seoul National University Hosp, Seoul, South Korea
Collaborators
Chugai Pharmaceutical
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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