Geneva, April 20 -- International Clinical Trials Registry received information related to the study (ChiCTR2600121697) titled 'A Phase 1, Randomized, Double-blinded, Placebo-Controlled, Single and Multiple Oral Doses Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of TAK-279 in Healthy Chinese Subjects' on April 1.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Huashan Hospital, Fudan University
Condition:
None
Intervention:
Cohort 1 (TAK-279 Group):TAK-279 30 mg, once daily (QD), oral
Cohort 1 (Placebo Group):Placebo, once daily (QD), oral
Cohort 2 (TAK-279 Group):TAK-279 60 mg, once daily (QD), oral
Recruitment Status: Not Recruiting
Phase: 1
Date of First Enrollment: 2024-06-24 ...