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

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Key facts

Sponsor
Wuhan Createrna Science and Technology Co., Ltd
Principal Investigator
Haiyan Li, PhD
PI
Intervention
MY008211A tablets(drug)
Enrollment
16 enrolled
Eligibility
18-45 years · All sexes
Timeline
20242024

Study locations (1)

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.

Open NCT06543459 on ClinicalTrials.gov

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