drugset / Trial / NCT06290050

A Study of the Interaction of Other Drugs With TAK-279 in Healthy Adults

NCT06290050

Phase 1 Completed 20 enrolled Takeda
Non-randomizedSequentialOpen-labelOther

Summary

The main aim of this study is to find out how several doses of TAK-279 affects the body of healthy adults and processes midazolam and repaglinide (pharmacokinetics or PK). Another aim is to learn about the side effects of TAK-279 and how well it is tolerated when given to healthy adults either alone or together with midazolam or repaglinide. During the study, participants will need to stay at the clinic for 19 days. Blood samples will be taken at several timepoints during the study. The study drug will be given by mouth (orally).

Timeline

Start
2024-03-29
Primary completion
2024-05-03
Completion
2024-05-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Midazolam Small molecule 2 mg Oral
Subject Repaglinide Small molecule 0.5 mg Oral
Subject Zasocitinib Small molecule Oral

Indications

No indication recorded.