RecruitingPhase 2NCT06298955
Long-Term Safety, Tolerability and Efficacy of OMS906 in 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
- Omeros Corporation
- Principal Investigator
- William PullmanOmeros Corporation
- Intervention
- OMS906 study drug(drug)
- Enrollment
- 25 enrolled
- Eligibility
- 18-99 years · All sexes
- Timeline
- 2024 – 2027
Study locations (5)
- Omeros Investigational Site, Aachen, Germany
- Omeros Investigational Site, Ulm, Germany
- Omeros Investigational Site, Lausanne, Switzerland
- Omeros Investigational Site, Kyiv, Ukraine
- Omeros Investigational Site, Leeds, 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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