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Atrium Therapeutics, Inc. news releases on 6ix. Latest, Jun 17, 2024: Avidity Biosciences, Inc. Announces Closing of Upsized Public Offering of Common Stock…

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Avidity Biosciences, Inc. Announces Closing of Upsized Public Offering of Common Stock, Including Full Exercise of Underwriters' Option to Purchase Additional Shares

June 16, 2024

Avidity Biosciences, Inc. Announces Pricing of Public Offering of Common Stock

June 12, 2024

Avidity Biosciences, Inc. Announces Proposed Public Offering of Common Stock

June 11, 2024

Avidity Announces Unprecedented AOC 1020 Data from Phase 1/2 FORTITUDE™ Trial Demonstrating Greater Than 50 Percent Reduction in DUX4 Regulated Genes and Trends of Functional Improvement in People Living with Facioscapulohumeral Muscular Dystrophy

June 11, 2024

Avidity Biosciences to Present Preliminary Data from Phase 1/2 FORTITUDE™ Trial of AOC 1020 in People Living with Facioscapulohumeral Muscular Dystrophy at 31st Annual FSHD Society International Research Congress

May 28, 2024

Avidity Biosciences Announces Appointment of Simona Skerjanec to Board of Directors

May 14, 2024

Avidity Biosciences Reports First Quarter 2024 Financial Results and Recent Highlights

May 8, 2024

Avidity Biosciences Receives FDA Breakthrough Therapy Designation for Delpacibart Etedesiran (AOC 1001) for Treatment of Myotonic Dystrophy Type 1

May 7, 2024

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

March 3, 2024

Avidity Biosciences Honors Rare Disease Day®

February 28, 2024

Avidity Biosciences Announces Oversubscribed $400 Million Private Placement

February 28, 2024

Avidity Biosciences Reports Fourth Quarter and Year-End 2023 Financial Results and Recent Highlights

February 27, 2024

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

February 19, 2024

Avidity Biosciences to Present New AOC 1001 Long-term Efficacy and Safety Data from MARINA-OLE™ Trial in People Living with Myotonic Dystrophy Type 1 (DM1) at 2024 Muscular Dystrophy Association (MDA) Clinical & Scientific Conference

February 14, 2024

Avidity Biosciences Announces 2024 Corporate Priorities and Catalysts for Next Stage of Growth

January 4, 2024

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

December 12, 2023

Avidity Biosciences Announces Expansion of Cardiovascular Collaboration with Bristol Myers Squibb for up to Five Targets Utilizing Avidity's Proprietary AOC™ Platform Technology

November 27, 2023

Avidity Biosciences Reports Third Quarter 2023 Financial Results and Recent Highlights

November 7, 2023

Avidity Biosciences Announces New Positive AOC 1001 Data Demonstrating Improvement in Multiple Additional Functional Endpoints and Favorable Long-term Safety and Tolerability in People with Myotonic Dystrophy Type 1

October 6, 2023

Avidity Biosciences Announces Upcoming Presentations at 28th Annual Congress of the World Muscle Society

September 25, 2023

Avidity Biosciences Joins with Patient Communities to Raise Awareness During National Muscular Dystrophy Awareness Month as it Advances Three Muscular Dystrophy Clinical Programs

September 6, 2023

Avidity Biosciences Announces Upcoming Presentations at 2023 Myotonic Dystrophy Foundation Annual Conference

August 30, 2023

Avidity Biosciences Receives FDA Orphan Drug Designation for AOC 1044 for Treatment of Duchenne Muscular Dystrophy in People with Mutations Amenable to Exon 44 Skipping

August 14, 2023

Avidity Biosciences Reports Second Quarter 2023 Financial Results and Recent Highlights

August 7, 2023

Avidity Biosciences Joins with Patients, Caregivers and Healthcare Providers Globally to Support World Facioscapulohumeral Muscular Dystrophy (FSHD) Day

June 19, 2023

Avidity Biosciences Announces Upcoming Presentations at the 30th Annual FSHD Society International Research Congress

June 7, 2023

Avidity Biosciences Announces FDA Eases Partial Clinical Hold on AOC 1001 Providing a Clear Path Forward to Finalize Pivotal Dose and Phase 3 Design in Adults with Myotonic Dystrophy Type 1

May 16, 2023

Avidity Biosciences Reports First Quarter 2023 Financial Results and Recent Highlights

May 8, 2023

Avidity Biosciences Announces Positive Topline Data from AOC 1001 Phase 1/2 MARINA™ Trial Demonstrating Functional Improvement, Disease Modification and Favorable Safety and Tolerability Profile in People Living with Myotonic Dystrophy Type 1

April 26, 2023

Avidity Biosciences Granted FDA Fast Track Designation for AOC 1044 for Treatment of Duchenne Muscular Dystrophy Mutations Amenable to Exon 44 Skipping

April 23, 2023

Avidity Biosciences Announces Upcoming Presentations at the 75th American Academy of Neurology Annual Meeting

April 16, 2023

Avidity Biosciences to Host Investor and Analyst Event Focused on AOC 1001 Topline Data from Phase 1/2 MARINA™ Trial on April 27, 2023

April 12, 2023

Avidity Biosciences Provides Regulatory Update on AOC 1001 for Myotonic Dystrophy Type 1 and Plans to Present Top-line Data from Phase 1/2 MARINA™ Trial at AAN Annual Meeting

March 29, 2023

Avidity Biosciences Announces Upcoming Presentations at 2023 MDA Clinical & Scientific Conference

March 12, 2023

Avidity Biosciences Reports Fourth Quarter and Year-End 2022 Financial Results and Recent Highlights

February 27, 2023

Avidity Advances RNA Programs and Expands into New Therapeutic Areas Utilizing its AOC™ Platform

February 26, 2023

Avidity Biosciences Announces Arthur A. Levin to Join Board of Directors and Transition to Distinguished Scientist and Strategic Leader

February 22, 2023

Avidity Biosciences Receives FDA Orphan Drug Designation for AOC 1020 for the Treatment of Facioscapulohumeral Muscular Dystrophy

February 13, 2023

Avidity Biosciences Granted FDA Fast Track Designation for AOC 1020 for the Treatment of Facioscapulohumeral Muscular Dystrophy

January 17, 2023

Avidity Biosciences, Inc. Announces Pricing of Upsized Public Offering of Common Stock

December 14, 2022

Avidity Announces Positive AOC 1001 Phase 1/2 MARINA™ Data Demonstrating First-Ever Successful Targeted Delivery of RNA to Muscle - Revolutionary Advancement for the Field of RNA Therapeutics

December 13, 2022

Avidity Biosciences Reports Third Quarter 2022 Financial Results and Recent Highlights

November 7, 2022

Avidity Biosciences Announces Phase 1/2 EXPLORE44™ Trial of AOC 1044 for Duchenne Muscular Dystrophy Mutations Amenable to Exon 44 Skipping

October 10, 2022

Avidity Biosciences Announces Upcoming Presentations at 27th International Hybrid Annual Congress of World Muscle Society

October 5, 2022

Avidity Biosciences Announces the Phase 1/2 FORTITUDE™ Trial of AOC 1020 in Adults with Facioscapulohumeral Muscular Dystrophy

September 28, 2022

Avidity Biosciences Announces FDA Partial Clinical Hold on New Participant Enrollment in Phase 1/2 MARINA™ Trial

September 26, 2022

Avidity Biosciences Engages with Patient Communities During National Muscular Dystrophy Awareness Month as part of Commitment to Developing Muscular Dystrophy Programs

September 6, 2022

Avidity Biosciences Reports Second Quarter 2022 Financial Results and Recent Highlights

August 8, 2022

Avidity Biosciences Enrolls Patients in the MARINA™ Open-Label Extension Study

August 1, 2022

Avidity Biosciences Supports World Facioscapulohumeral Muscular Dystrophy (FSHD) Day and Presents Preclinical Data from FSHD Program

June 16, 2022

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