CompletedPhase 1NCT05828472
A Study of Multiple Ascending Doses MY008211A in Healthy Adults
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
- Wuhan Createrna Science and Technology Co., Ltd
- Principal Investigator
- Wei feng, Ph.DWuhan Createrna Science and Technology Co., Ltd
- Intervention
- MY008211A tablets(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2023 – 2023
Study locations (1)
- The Third Hospital of Changsha, Changsha, Hunan, China
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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