Duchenne Muscular Dystrophy – Drugs In Development, 2024
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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.
The Duchenne Muscular Dystrophy drugs in development market research report provide 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. The report also covers the descriptive pharmacological action and product description of the therapeutics, and the latest news and press releases. Additionally, the report provides an overview of key players involved in therapeutic development for Duchenne Muscular Dystrophy and features dormant and discontinued products.
Note:
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* Certain sections in the report may be removed or altered based on the availability and relevance of data.
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Scope
- Therapeutics in Development: Covering 198 molecules, with 175 developed by companies and the rest by universities/institutes.
- Analysis Parameters: Offering insights by stage of development, drug target, MoA, RoA, and molecule type for a comprehensive overview.
- Pharmacological Insights: Understand the descriptive pharmacological action of therapeutics.
- Development History: Access the complete research and development history.
- Latest News and Press Releases: Stay updated with the latest developments through comprehensive news coverage.
Reasons to Buy
- Holistic insights: Understand the broad spectrum of Duchenne Muscular Dystrophy therapeutics, aiding strategic decision-making with insights into stages, targets, MoA, RoA and molecule types.
- Pipeline Exploration: Explore the detailed Duchenne Muscular Dystrophy pipeline, offering nuanced analysis of drug targets, mechanisms of action and routes of administration for varied decision-making.
- Comprehensive R&D: Access thorough R&D histories, providing a comprehensive understanding of Duchenne Muscular Dystrophy treatments for adaptable decision-making.
- Save valuable hours: Identify key players steering innovation in therapeutics, enabling strategic partnerships.
Key Players
AAVogen IncADEL Inc
Allagium therapeutics Inc
Alpha Anomeric
American CryoStem Corp
AMO Pharma Ltd
Anagenesis Biotechnologies SAS
Antisense Therapeutics Ltd
ARMGO Pharma Inc
ART BioScience
Astria Therapeutics Inc
AUM LifeTech Inc
Autotac Bio Inc
Avidity Biosciences Inc
Axolo Pharma Inc
BioIncept LLC
Bioleaders Corp
BioMarin Pharmaceutical Inc
Biophytis SA
CANbridge Life Sciences Ltd
Capricor Therapeutics Inc
ChemIcare Srl
Chengdu Fanxi Biopharma Co Ltd
Chengdu Genevector Biotechnology Co Ltd
Code Biotherapeutics Inc
Consortium.AI
Constant Therapeutics LLC
Cumberland Pharmaceuticals Inc
Curamys Co Ltd
Cure Rare Disease
Daiichi Sankyo Co Ltd
DR.Noah Biotech Inc
Dyne Therapeutics Inc
Dystrogen Therapeutics SA
ECM Therapeutics Inc
Edgewise Therapeutics Inc
Editas Medicine Inc
Eli Lilly and Co
Eloxx Pharmaceuticals Inc
Encell Co Ltd
Entrada Therapeutics Inc
Epirium Bio Inc
EspeRare Foundation
FibroGenesis LLC
Fulcrum Therapeutics Inc
Genethon SA
Harvard University
hC Bioscience Inc
HuidaGene Therapeutics Co Ltd
ImmunoForge Co Ltd
Imstem Biotechnology Inc
Inmune Bio Inc
InnoBioscience LLC
Insmed Inc
Intas Pharmaceuticals Ltd
IPS Heart Inc
Italfarmaco SpA
Ixchel Pharma LLC
J2H Biotech
JAR of Hope
Juvena Therapeutics Inc
Kaneka Corp
Keros Therapeutics Inc
Korea Pharma Co Ltd
Korea University
KSbitugen Co Ltd
LambdaGen Therapeutics
Les Laboratoires Servier SAS
Locanabio Inc
Ludi Therapeutics
MetrioPharm AG
Mitobridge Inc
Mitochon Pharmaceuticals Inc
MitoRx Therapeutics Ltd
MyoGene Bio LLC
Myogenica Inc
Myos Inc
Myosana Therapeutics Inc
Nippon Shinyaku Co Ltd
Northwestern University
Novo Biosciences Inc
NS Pharma Inc
NTrans Technologies BV
OliPass Corporation
OMEICOS Therapeutics GmbH
Oncotelic Therapeutics Inc
Orna Therapeutics Inc
Pepgen Inc
PeptiDream Inc
Perelman School of Medicine at the University of Pennsylvania
Pfizer Inc
Pliant Therapeutics Inc
Prime Medicine Inc
Progenitor Therapeutics Ltd
Prothelia Inc
PTC Therapeutics Inc
PYC Therapeutics Ltd
Quince Therapeutics Inc
Ractigen Therapeutics Inc
RASRx LLC
RegenxBio Inc
ReoStem LLC
Ridgeline Therapeutics LLC
Royal Holloway University of London
Santhera Pharmaceuticals Holding AG
Sarcomed AB
Sarepta Therapeutics Inc
Satellos Bioscience Inc
SiVEC Biotechnologies LLC
Solid Biosciences Inc
SOM Biotech SL
Sqy Therapeutics SA
Stanford University
Stealth BioTherapeutics Inc.
Stem Cells of Arabia
SteroTherapeutics LLC
Strykagen Corp
Sutura Therapeutics Ltd
Suzhou GenAssist Therapeutics Co Ltd
Taiho Pharmaceutical Co Ltd
Technical University of Munich
Tevard Biosciences LLC
The Hospital for Sick Children
Tivorsan Pharmaceuticals Inc
Tolerion Inc
Triplex Therapeutics Inc
UGISense AG
Ultragenyx Pharmaceutical Inc
University Children's Hospital Basel
University of Alberta
University of California Los Angeles
University of Exeter
University of Pennsylvania
University of Queensland
University of Wisconsin Madison
Vertex Pharmaceuticals Inc
Vita Therapeutics Inc
Vitti Labs LLC
Wave Life Sciences Ltd
Zata Pharmaceuticals Inc
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