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Duchenne Muscular Dystrophy

Biotech News

Elevidys 3-Year Trial Data Show Sustained Outcomes in DMD Patients

January 30, 2026
Diagnostics News

HHS Expands Newborn Screening to Include Duchenne and MLD

December 19, 2025
Biotech News

FDA Places New Restrictions on Sarepta’s Elevidys Gene Therapy After DMD Patient Deaths

November 19, 2025
Biotech News

Novartis Acquires Avidity Biosciences for Late-Stage Muscular Dystrophy Assets in $12B Deal

October 31, 2025
Biotech News

Sarepta Cuts 36% of Workforce and Finally Agrees to FDA Request to Halt All Elevidys Shipments Following Patient Deaths

July 23, 2025
Biotech News

Sarepta’s Gene Therapy Elevidys Under Scrutiny After Patient Death

March 19, 2025
Blogs

Best Pharma Innovations of 2024, According to TIME

November 7, 2024
Biotech News

GUARDIAN Study Reveals How Genomic Sequencing Could Bridge Gaps in Newborn Screening

October 29, 2024
Biotech Blogs

Elixirgen Therapeutics’ Innovative Approach to mRNA Therapeutics

June 18, 2024
Approvals News

Italfarmaco’s Duvyzat Wins FDA Approval as First Nonsteroidal Treatment for All Genetic Variants of DMD

March 28, 2024
Approvals News

Sarepta’s Elevidys Reaches Finish Line as First Gene Therapy Approved for Duchenne Muscular Dystrophy

June 28, 2023

The Patient Experience Using MRI in DMD Clinical Trials — “Shed light through MRI”

April 21, 2022

Imaging for Neuromuscular Disorders in Clinical Trials

December 07, 2021
Biotech News

New CRISPR Gene Editing Enzyme Removed Duchenne Muscular Dystrophy Mutations

September 17, 2018
Biotech News

Watch Out Sarepta: Pfizer Initiates Trial of Duchenne Muscular Dystrophy Gene Therapy

August 30, 2018
Biotech News

Mallinckrodt Starts Phase II Duchenne Muscular Dystrophy Study but Will They Meet Recruitment Targets?

August 3, 2018
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