TerminatedPhase 2NCT05741346
Long-term Safety of BCX9930 in 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
- BioCryst Pharmaceuticals
- Principal Investigator
- Phillip Scheinberg, MD, PhDBeneficência Portuguesa de São Paulo
- Intervention
- BCX9930(drug)
- Enrollment
- 28 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2025
Study locations (11)
- Investigative Site, Paris, France
- Investigative Site, Budapest, Hungary
- Investigative Site, Ampang, Malaysia
- Investigative Site, Bloemfontein, South Africa
- Investigative Site, Cape Town, South Africa
- Investigative Site, Pretoria, South Africa
- Investigative Site, Daejeon, South Korea
- Investigative Site, Barcelona, Spain
- Investigative Site, Valencia, Spain
- Investigative Site, Leeds, United Kingdom
- Investigative Site, London, United Kingdom
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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