CompletedPhase 1NCT04818398

Study of Single-Ascending Doses of DS-6016a in Healthy Japanese Subjects

Studying Fibrodysplasia ossificans progressiva

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Key facts

Sponsor
Daiichi Sankyo Co., Ltd.
Principal Investigator
Global Clinical Leader
Daiichi Sankyo
Intervention
DS-6016a(drug)
Enrollment
48 enrolled
Eligibility
20-45 years · MALE
Timeline
20212022

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 NCT04818398 on ClinicalTrials.gov

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