The Duchenne Muscular Dystrophy drugs in development market research report provides comprehensive information on the therapeutics under development for Duchenne Muscular Dystrophy, complete with analysis by stage of development, drug target, mechanism of action (MoA), route of administration (RoA), and molecule type. GlobalData’s report assesses key aspects of the companies and drugs in development for Duchenne Muscular Dystrophy. Buy the report here.
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The report also covers the descriptive pharmacological action of the therapeutics and the latest news and press releases. Additionally, the report provides an overview of the key players involved in therapeutic development for Duchenne Muscular Dystrophy and features dormant and discontinued products.
GlobalData tracks 196 drugs in development for Duchenne Muscular Dystrophy by 137 companies/universities/institutes. The top development phase for Duchenne Muscular Dystrophy is preclinical with 101 drugs in that stage. The Duchenne Muscular Dystrophy pipeline has 176 drugs in development by companies and 20 by universities/ institutes. Some of the companies in the Duchenne Muscular Dystrophy pipeline products market are: Sarepta Therapeutics, Dyne Therapeutics and Entrada Therapeutics.
The key targets in the Duchenne Muscular Dystrophy pipeline products market include Dystrophin, Utrophin, and Glucocorticoid Receptor.
The key mechanisms of action in the Duchenne Muscular Dystrophy pipeline product include Dystrophin Activator with 79 drugs in Pre-Registration. The Duchenne Muscular Dystrophy pipeline products include ten routes of administration with the top ROA being Intravenous and 13 key molecule types in the Duchenne Muscular Dystrophy pipeline products market including Antisense Oligonucleotide, and Small Molecule.
Duchenne Muscular Dystrophy overview
Duchenne muscular dystrophy (DMD) is a genetic disorder that causes muscles to gradually weaken over time. Signs and symptoms of DMD include fatigue, learning difficulties, intellectual disability, muscle weakness, and progressive difficulty walking. Risk factors include gender and family history. Treatments include steroid medication, respiratory therapy, and surgery.
For a complete picture of Duchenne Muscular Dystrophy’s pipeline drug market, buy the report here.
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GlobalData’s pipeline drugs offers detailed profiles of pharmaceutical drugs in all stages of pre-clinical and clinical development, from discovery through to pre-registration. Coverage is limited to novel human medicinal drugs and biosimilars seeking market approval proprietary and is one of two primary repositories of pharmaceutical drug information offered by GlobalData through its Pharmaceutical Intelligence Center.
