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0.0470459518599562 -0.0787746170678338 -0.157549234135667 -0.388402625820569 -0.25492341356674 -0.222100656455142 -0.231947483588621 -0.217724288840263
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Enanta Pharmaceuticals Reports Positive Topline Results from its Phase 2b Study of Zelicapavir for the Treatment of Respiratory Syncytial Virus (RSV) in High-Risk Adults

Enanta Pharmaceuticals, Inc. (ENTA) 
Last enanta pharmaceuticals, inc. earnings: 2/6 04:00 pm Check Earnings Report
US:NASDAQ Investor Relations: ir.enanta.com/investor-overview
Company Research Source: Business Wire
6.7-Day Improvement in Time to Complete Resolution of All RSV Symptoms for Patients with Chronic Obstructive Pulmonary Disease (COPD), Congestive Heart Failure (CHF), or Age =75Statistically Significant Improvement in Patient Global Impression of Severity ScoreLower Hospitalization Rate for Patients Treated with Zelicapavir (1.7%) vs. Placebo (5%)4- to 5-Day Faster Median Time to Undetectable Viral Load with Zelicapavir vs. PlaceboManagement to Host Conference Call and Webcast Today at 8:30 a.m. ET WATERTOWN, Mass.--(BUSINESS WIRE)--Enanta Pharmaceuticals, Inc. (NASDAQ: ENTA), a clinical-stage biotechnology company dedicated to creating small molecule drugs for viral infections and immunological diseases, today announced positive topline data from RSVHR, a Phase 2b, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of zelicapavir in outpatient adults with acute RSV infection who are at high risk of complications including the elderly and/or thos Show less Read more
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