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A Randomized, Open-Label, Six-Sequence, Three-Period Crossover Study to Demonstrate the Bioequivalence of Single Oral Administration of K-001 Relative to Single Oral Coadministration of Separate Tablets of K-877-ER Plus CSG452 in Healthy Adult Volunteers, and to Characterize the Food Effect on the Pharmacokinetics of K-001
Conditions
Interventions
K-001
K-877-ER
+1 more
Locations
1
United States
PPD - Austin Research Unit
Austin, Texas, United States
Start Date
February 24, 2023
Primary Completion Date
April 1, 2023
Completion Date
April 5, 2023
Last Updated
June 2, 2023
NCT07310264
NCT06716502
NCT06290258
NCT00090662
NCT07483606
NCT06342713
Lead Sponsor
Kowa Research Institute, Inc.
Data Source & Attribution
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