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US05370A1088

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08/05	Avidity Biosciences Receives FDA Breakthrough Therapy Designation for Treatment of Myotonic Dystrophy Type 1	MT
08/05	Avidity's Lead Program Gets FDA Breakthrough Designation	DJ

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Avidity's Lead Program Gets FDA Breakthrough Designation	08/05	DJ
Avidity Biosciences, Inc. Receives FDA Breakthrough Therapy Designation for Delpacibart Etedesiran (AOC 1001) for Treatment of Myotonic Dystrophy Type 1	08/05	CI
Avidity Biosciences Announces Positive Aoc 1001 Long-Term Data Showing Reversal of Disease Progression in People Living with Myotonic Dystrophy Type 1 Across Multiple Endpoints; Same Key Endpoints Agreed for Phase 3 Harbor? Trial	04/03	CI
Apprehension About Key Inflation Data Pushes Exchange-Traded Funds, Equity Futures Lower Pre-Bell Thursday	29/02	MT
Avidity Biosciences, Inc. Reports Earnings Results for the Full Year Ended December 31, 2023	29/02	CI
Avidity Biosciences, Inc. Reports Earnings Results for the Fourth Quarter Ended December 31, 2023	29/02	CI
Avidity Biosciences Receives FDA Rare Pediatric Disease Designation for AOC 1044 for Treatment of Duchenne Muscular Dystrophy in People with Mutations Amenable to Exon 44 Skipping	20/02	CI
Avidity Biosciences, Inc. Plans to Initiate the Global Phase 3 Harbour Trial of AOC 1001 for Adults Living with Myotonic Dystrophy Type 1, in Mid-2024	05/01	CI
Avidity Biosciences Reports Positive Data Demonstrating Aoc 1044 Delivers Unprecedented Concentrations of Pmo in Muscle Following A Single Dose in Healthy Volunteers from Phase 1/2 Explore44? Trial for Duchenne Muscular Dystrophy	13/12	CI
Avidity Biosciences Collaborates With Bristol Myers to Advance Use of AOC in Multiple Cardiac Targets	28/11	MT
Avidity Biosciences, Inc. Announces Expansion of Cardiovascular Collaboration with Bristol Myers Squibb for Up to Five Targets Utilizing Avidity's Proprietary AOC Platform Technology	28/11	CI
Avidity Biosciences, Inc. Reports Earnings Results for the Third Quarter and Nine Months Ended September 30, 2023	09/11	CI
Avidity Biosciences, Inc. Presents New Data Regarding Its Clinical Study of AOC 1001 for Adults with Myotonic Dystrophy Type 1	10/23/10	CI
Avidity Biosciences Gets FDA Orphan Drug Label For AOC 1044 in Muscular Dystrophy	15/23/15	MT
Avidity Biosciences, Inc. Reports Earnings Results for the Second Quarter and Six Months Ended June 30, 2023	09/23/09	CI
Avidity Biosciences, Inc. Provides an Update to the Status of the Partial Clinical Hold Related to Its AOC 1001 Product Candidate	17/23/17	CI
Avidity Biosciences, Inc. Reports Earnings Results for the First Quarter Ended March 31, 2023	10/23/10	CI
Avidity Biosciences Announces Positive Topline Data from Aoc 1001 Phase 1/2 Marine Trial Demonstrating Functional Improvement, Disease Modification and Favorable Safety and Tolerability Profile in People Living with Myotonic Dystrophy Type 1	28/23/28	CI
Avidity Biosciences Secures FDA Fast Track Designation for AOC 1044	24/23/24	MT
US drugmakers call for reversing Texas abortion pill ruling	10/23/10	RE

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