Evaluate the Effect of Vimseltinib on Organic Cation Transporter 2 (OCT2)
Completed · Phase 1
Conditions studied: Healthy Participants
In brief
The main purpose of this study is to evaluate the effect of multiple doses of vimseltinib on the pharmacokinetics (PK) of a clinical OCT2 substrate (metformin) in healthy male participants. This study will also assess the safety and tolerability when vimseltinib is co-administered with the clinical OCT2 substrate (metformin) in healthy male participants. This study will last approximately 25 days.
Key facts
- Study ID
- NCT07158411
- Run by
- Deciphera Pharmaceuticals, LLC
- People needed
- 22
- Starts
- 2025-11-20
- Expected to finish
- 2026-01-30
- Last updated by the study team
- 2026-02-11
Who can join
Age: 18 and older, up to 55. Sex: male. Healthy volunteers: accepted.
You may qualify if…
- Body mass index (BMI) from 18 to 32 kilogram per square meter (kg/m\^2).
- Participants are in good general health, as required by the protocol and as determined by Principal Investigator.
- Adequate organ function and blood and urine tests, as required by the protocol and as determined by Principal Investigator.
You may not qualify if…
- History or presence of clinically significant diseases of the neurological, dermatological, renal, hepatic, gastrointestinal, cardiovascular, or musculoskeletal systems and/or history or presence of clinically significant psychiatric, immunological, endocrine, or metabolic disease in the opinion of the Investigator.
- Unwilling or unable to comply with the requirements of the protocol.
- Determined by Principal Investigator to be unsuitable to participate in the study for any other reason.
Where it is running
- Dr. Vince Clinical Research — Overland Park, Kansas, United States
Full record on ClinicalTrials.gov
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