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Alnylam Announces New Positive Interim Phase 1 Study Results for Fitusiran, a Once-Monthly, Subcutaneous, Investigational RNAi Therapeutic Targeting Antithrombin for the Treatment of Hemophilia and Rare Bleeding Disorders (Alnylam Pharmaceuticals Inc)

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(Source: Alnylam Pharmaceuticals Inc) 07.25.2016 - Fitusiran Achieves Median Estimated Annualized Bleeding Rate of Zero in Patients without Inhibitors - - In Initial Low Dose Cohort of Patients with Inhibitors, Fitusiran Achieves Antithrombin Lowering, Increased Thrombin Generation, and Preliminary Evidence for Reduced Bleeding - - Fitusiran Administration Generally Well Tolerated in Hemophilia Patients with and without Inhibitors - - Company Updates Guidance for Phase 3, and Now Plans to Start Studies in Early 2017 - - Company has Rescheduled its Conference Call, which will Now Occur Today, Monday, July 25, at 1:00 pm ET - CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Alnylam Pharmaceuticals, Inc....

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