Condition: Chronic Coronary Syndrome · Sponsor: Viatris Innovation GmbH
The purpose of this study is to evaluate the pharmacokinetics (PK), pharmacodynamics, and tolerability of a single dose of selatogrel in Chinese adults with chronic coronary syndrome. Pharmacokinetics is the study of the absorption and breakdown of the study drug in the body. Pharmacodynamics is the study of the effect of the study drug on the body. Researchers will compare selatogrel to a placebo (a look-alike substance that contains no drug). Participants will stay at the research clinic for 3 or 4 days (2 or 3 nights), during which time they will receive a single dose of selatogrel or placebo. A telephone call for post-trial safety follow-up will be done 30-40 days after the participant leaves the clinic.
This description comes directly from the study's public registry record.
Viatris Innovation Clinical Trial Information · +1 833 643 8188 · viatrisinnovationclinicaltrials@viatris.com
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| Anzhen Hospital | Beijing, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07615868