Duchenne Muscular Dystrophy
Research Highlights/News
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2024:
Press Releases:
2023:
Press Releases:
- CDMRP-Funded Research Contributed to a Recently FDA-Approved Drug for Duchenne Muscular Dystrophy
November 3, 2023
Research Highlights:
2022:
Press Releases:
2021:
Press Releases:
Research Highlights
News:
- Santhera and ReveraGen Announce Positive and Statistically Highly Significant Topline Results with Vamorolone in Pivotal VISION-DMD Study (external link)
Santhera, June 7, 2021
2020:
Press Releases:
Research Highlights
News:
- Completion of Long-Term Extension Study with Vamorolone in Duchenne Muscular Dystrophy (external link)
Santhera, June 3, 2020 - JAMA Neurology Publication of Clinical Trial Data for Viltolarsen in DMD Patients (external link)
CISION PR Newswire, May 29, 2020
2019:
Press Releases:
News:
- CRISPR Fix in Mice May Lead to Muscular Dystrophy Therapy (external link)
Futurity, October 8, 2019 - Vamorolone Treatment of Duchenne Muscular Dystrophy Patients Leads to Improvements in Motor Function (external link)
ReveraGen, September 6, 2019 - Single CRISPR Treatment Provides Long-Term Benefits in Mouse Models of Duchenne (external link)
Duke University - Pratt School of Engineering, February 22, 2019 - Researchers Overcome Hurdle in CRISPR Gene Editing for Muscular Dystrophy (external link)
University of Missouri Health, January 15, 2019
2018:
Press Releases:
Research Highlights
News:
- Investigational steroid mirrors prednisone's benefits while taming its side effects (external link)
EurekAlert!, September 25, 2018
2017:
Press Releases:
- Department of Defense Duchenne Muscular Dystrophy Research Program Anticipated Funding Opportunities for Fiscal Year 2017 (FY17)
March 31, 2017
Research Highlights
News:
- FDA Grants RASRx1902 Orphan Drug Status as Potential Therapy for Duchenne Muscular Dystrophy (external link)
Muscular Dystrophy News Today, June 23, 2017
2016:
Press Releases:
News:
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Actelion obtains an option to in-license vamorolone, a novel treatment for Duchenne, from ReveraGen (external link)
ReveraGen, November 14, 2016 -
Gene editing offers hope for treating Duchenne Muscular Dystrophy (external link)
The New York Times, January 11, 2016
2015:
Press Releases:
2014:
Press Releases:
2013:
Press Releases:
- Department of Defense Duchenne Muscular Dystrophy Research Program Funding Opportunities for Fiscal Year 2013 April 19, 2013
Research Highlights:
- A Potential New DMD Therapeutic
- DMD Diagnostic Optical Imaging
- New Clinical Outcome Measurements
- GALGT2 Gene Therapy
News:
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New Muscular Dystrophy Treatment Shows Promise in Early Study Led by Children's National (external link)
Children's National Health System, October 2, 2013
2012:
Press Releases:
- Department of Defense Duchenne Muscular Dystrophy Research Program Funding Opportunities for Fiscal Year 2011 August 23, 2011
News:
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Sarepta Therapeutics Announces Significant Clinical Benefit With Eteplirsen (external link)
Sarepta Therapeutics, August 17, 2012
Last updated Tuesday, October 8, 2024