Not yet recruitingPhase 1NCT06543459
To Evaluate the Effect of Single Oral Dose of MY008211A Tablets on QTc Interval in Healthy Subjects
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
- Haiyan Li, PhDPI
- Intervention
- MY008211A tablets(drug)
- Enrollment
- 16 enrolled
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2024 – 2024
Study locations (1)
- Peking University Third Hospital, Beijing, Beijing Municipality, 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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