A Study of MK-2225 in Healthy Participants (MK-2225-003)
Completed · Phase 1 · Has a placebo group
Conditions studied: Systemic Sclerosis
In brief
The purpose of the study is to learn about the safety of MK-2225, including how well people tolerate it. Researchers also want to learn what happens to different doses of MK-2225 in a person's body over time.
Key facts
- Study ID
- NCT06643390
- Run by
- Merck Sharp & Dohme LLC
- People needed
- 32
- Starts
- 2023-11-21
- Expected to finish
- 2025-07-14
- Last updated by the study team
- 2025-07-29
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- The key inclusion criteria include but are not limited to the following:
- Is in good health before randomization
- Body Mass Index (BMI) ≤32 kg/m\^2, inclusive
You may not qualify if…
- The key exclusion criteria include but are not limited to the following:
- History of clinically significant endocrine, gastrointestinal (GI), cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological (including stroke and chronic seizures) abnormalities or diseases
- History of hypersensitivity to the MK-2225 drug substance, its inactive ingredients or the placebo (normal saline)
Where it is running
- Clinical Pharmacology of Miami (Site 0002) — Miami, Florida, United States
- Bio-Kinetic Clinical Applications, LLC dba QPS-MO (Site 0004) — Springfield, Missouri, United States
Full record on ClinicalTrials.gov
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