MDA Summer Camp
Registration Opens for MDA Summer Camp for Children with Neuromuscular Diseases
January 17, 2023 09:00 ET | Muscular Dystrophy Association
New York, NY, Jan. 17, 2023 (GLOBE NEWSWIRE) -- The Muscular Dystrophy Association (MDA) announced today the opening of registration for its MDA Summer Camp program for children ages 8 to 17 living...
2023 MDA Clinical & Scientific Conference Keynote Speaker
FDA’s Peter Marks, M.D., Ph.D. to deliver Keynote Address at 2023 Muscular Dystrophy Association Clinical & Scientific Conference
January 10, 2023 06:00 ET | Muscular Dystrophy Association
New York, NY, Jan. 10, 2023 (GLOBE NEWSWIRE) -- The Muscular Dystrophy Association (MDA) today announced Peter Marks, M.D., Ph.D. as the Keynote Speaker at the MDA 2023 Clinical & Scientific...
MDA Board of Directors Announcement
Muscular Dystrophy Association Elects Governor Brad Henry as Chairman and Christopher Rosa, Ph.D. as Vice Chairman of the Board of Directors
January 09, 2023 09:20 ET | Muscular Dystrophy Association
New York, NY, Jan. 09, 2023 (GLOBE NEWSWIRE) -- The Muscular Dystrophy Association (MDA) announced today the election of new Board of Directors leadership. Governor Brad Henry will now serve as...
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Duchenne Muscular Dystrophy Market to Hit Sales of $1533.72 Million by 2028 | DMD Affects 250,000 Children Each Year | Gene Therapy is the Only effective Way to Treat DMD
September 28, 2022 10:22 ET | SkyQuest Technology Consulting Pvt. Ltd.
Westford,USA, Sept. 28, 2022 (GLOBE NEWSWIRE) -- There is an increasing demand for Duchenne muscular dystrophy (DMD) therapies, as the condition is still not curable. In the medical industry, there...
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miRecule Inc. closes $5.7 M to Create Breakthrough RNA Therapies for Cancer and Muscular Dystrophy
May 27, 2021 11:07 ET | miRecule
GAITHERSBURG, Md., May 27, 2021 (GLOBE NEWSWIRE) -- miRecule, Inc. (“miRecule”), an emerging biotech company focused on the development of cutting-edge RNA therapeutics, announced today it has...
Matt Alsante_AskBio Patient Advocacy
AskBio Launches AskFirst™ Patient Advocacy Program to Educate and Support Participants in Gene Therapy Clinical Trials
January 29, 2020 10:27 ET | Asklepios BioPharmaceutical, Inc.
RESEARCH TRIANGLE PARK, N.C., Jan. 29, 2020 (GLOBE NEWSWIRE) -- Asklepios BioPharmaceutical, Inc. (AskBio), a clinical-stage adeno-associated virus (AAV) gene therapy company, today introduced...
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Going the Distance for Duchenne
July 09, 2019 15:34 ET | Jett Foundation
Plymouth, MA, July 09, 2019 (GLOBE NEWSWIRE) -- A group of inspiring young people will join Jett Foundation, a non-profit organization dedicated to awareness and helping fight Duchenne muscular...
MDA Awards $300,000
MDA Awards $300,000 to Streamline Gathering of Data for ALS Research
June 15, 2017 16:24 ET | Muscular Dystrophy Association
Chicago, June 15, 2017 (GLOBE NEWSWIRE) -- The Muscular Dystrophy Association has announced the award of a clinical research network grant (CRNG) to Michael Benatar, M.D., Ph.D., at the University...
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Gala Global to Finalize Initial Hemp "CBD" Products
February 11, 2015 08:00 ET | Gala Pharmaceutical Inc.
LOS ANGELES, Feb. 11, 2015 (GLOBE NEWSWIRE) -- Gala Global, Inc. (OTCQB:GLAG) today announced it has finalized the initial CBD products. The initial products will based on flavored infused CBD Oral...
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Prosensa announces Lancet Neurology publication of an exploratory phase II study (DEMAND II) demonstrating efficacy and safety of drisapersen in patients with Duchenne muscular dystrophy
September 08, 2014 08:00 ET | Prosensa Holding N.V.
Leiden, The Netherlands, Sept. 8, 2014 (GLOBE NEWSWIRE) -- LEIDEN, The Netherlands - September 8, 2014 - Prosensa Holding N.V. (NASDAQ: RNA), the biopharmaceutical company focusing on RNA-modulating...