Dyne is eyeing an accelerated approval filing for DYNE-251 in early 2026 that would pit the asset against Sarepta’s Exondys ...
Avidity Biosciences (RNA) announced del-zota topline data from the Phase 1/2 EXPLORE44 trial in people living with Duchenne muscular dystrophy ...
Avidity Biosciences (RNA) announced positive del-zota topline data from the Phase 1/2 EXPLORE44 trial in people living with Duchenne muscular ...
Avidity Biosciences, Inc. (Nasdaq: RNA), a biopharmaceutical company committed to delivering a new class of RNA therapeutics ...
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GlobalData on MSNDyne’s DMD trial advances patient mobility and dystrophin expressionThe Phase I/II trial sought to establish the impact of DYNE-251 on mobility-related endpoints, seeing an increase over ...
PGN-EDO51 is designed to skip exon 51 of the dystrophin transcript, an established therapeutic target for approximately 13% of DMD patients, thereby aiming to restore the open reading frame and ...
Oral Presentations Title: CONNECT1-EDO51: A 12-Week Open-Label Phase 2 Study to Evaluate PGN-EDO51 Safety and Efficacy in People with Duchenne Amenable to Exon 51 Skipping Session: Clinical Trial ...
Sarepta Therapeutics (NASDAQ:SRPT – Free Report) had its target price lowered by Scotiabank from $105.00 to $80.00 in a ...
Data from the 5mg/kg cohort, released in July 2024, showed the therapy to be well-tolerated, with patients showing early signs of efficacy, including a mean exon skipping level of 2.15% and a 0.26 ...
While data on functional endpoints are still to come, Avidity Biosciences Inc. executives said the firm is moving ahead with ...
A University of Alberta research team has taken the first step toward proving its innovative gene therapy can successfully ...
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