TerminatedPhase 3NCT03829449
rVA576 (Coversin) Long Term Safety and Efficacy Surveillance Study
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
- AKARI Therapeutics
- Principal Investigator
- Wynne Weston DaviesAKARI Therapeutics
- Intervention
- rVA576(drug)
- Enrollment
- 15 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2020
Study locations (1)
- Instytut Hematologii i Transfuzjologii, Warsaw, Poland
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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