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Olatorepatide Obesity Treatment Licensed by Regeneron Demonstrates Positive Phase 3 Results in Chinese Patients

Patients treated with olatorepatide achieved up to 19% body-weight loss at week 48 Regeneron’s global Phase 3 registrational program to be initiated later this year TARRYTOWN, N.Y., March 09, 2026 (GLOBE NEWSWIRE) -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced Hansoh Pharmaceutical Group Company Limited has shared positive topline data from its Phase 3 trial in Chinese patients evaluating olatorepatide for the treatment of adults with obesity or who are overweight. Olatorepati

articleHansoh Pharmaceutical Group Company LimitedMarch 9, 20264/company/hansoh-pharmaceutical-group-co-ltd/news/olatorepatide-obesity-treatment-licensed-by-regeneron-demonstrates-positive-phase-3-results-in-chinese-patients-1
Olatorepatide Obesity Treatment Licensed by Regeneron Demonstrates Positive Phase 3 Results in Chinese Patients

About this update from Hansoh Pharmaceutical Group Company Limited

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Regeneronweight lossHansoh Pharmaceutical Group Company Limitedclinical developmentmulticenter trialChinese Mainlandobesitybody-weightdevelopmentcommercial rightsplacebodata analysis