Merck’s Lagevrio (molnupiravir) Missed Primary Endpoints in P-III Trial (MOVe-AHEAD) for Post-Exposure Prophylaxis to Prevent COVID-19
- The P-III trial (MOVe-AHEAD) evaluating Lagevrio (800mg) vs PBO in 1500 patients aged 18yrs. who were free of COVID-19 & lived with someone who was recently diagnosed with the virus
- The trial failed to meet its 1EPs i.e., the therapy did not show a significant reduction in the risk of COVID-19, following household exposure to another individual with COVID-19 while patients with Lagevrio were observed to be 23.6% less likely to develop COVID-19 than PBO @14 Day who did not have evidence of SARS-CoV-2 inf. at baseline
- The safety profile was consistent with prior reported studies & the company plans to submit full results at a scientific meeting. Lagevrio was approved or authorized in multiple markets incl. the US, UK, Australia, China & Japan
Ref: Merck | Image: Merck
Related Post:- Merck and Ridgeback Report Results for Lagevrio in P-II Studies for the Treatment of COVID-19
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