
Merck Cholesterol, Cancer Drugs May Enter FDA Fast-Track Program: Report

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The FDA plans to fast-track reviews of Merck's cholesterol and cancer drugs, enlicitide decanoate and sacituzumab tirumotecan, under the priority voucher program. This could accelerate approval timelines, with Merck expected to submit applications next year. The program shortens review time from 10-12 months to 1-2 months, enhancing regulatory decisions for critical medicines. Merck's stock rose 0.59% following the news.
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