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MK-6552 is an orally bioavailable small molecule drug developed by Merck Sharp & Dohme for the treatment of narcolepsy, specifically narcolepsy type 1. Its precise mechanism of action has not been disclosed or remains undefined. Clinical development reached Phase 1, with studies evaluating its safety, efficacy, pharmacokinetics (PK), and pharmacodynamics (PD) in both healthy volunteers and patients with narcolepsy. As of late 2024, clinical trials in the United States were terminated due to business reasons rather than safety or efficacy concerns[1][2][5][7][8].
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