The elevidys market has seen considerable growth due to a variety of factors.
• Recent years have seen the elevidys market size expand at a HCAGR of XX. Growth is set to continue, with projections indicating an increase from $XX million in 2024 to $XX million in 2025, corresponding to a compound annual growth rate (CAGR) of XX%.
Factors contributing to this historic growth include a rising incidence of Duchenne muscular dystrophy, amplified awareness campaigns, a surge in disease prevalence, an uptick in research and development activities, and rising healthcare expenditure.
The elevidys market is expected to maintain its strong growth trajectory in upcoming years.
• Expectations for the elevidys market size predict a growth to $XX million by 2029, with a compound annual growth rate (CAGR) of XX%.
This projected growth over the coming years can be linked to heightened investments in the discovery and development of innovative therapies. Contributing factors also include a burgeoning healthcare infrastructure, increased approvals from food and drug administration bodies, substantial demand from ambulatory and non-ambulatory Duchenne Muscular Dystrophy patients, and improved access and reimbursement rates. Key trends for the forecast period encompass novel therapeutic strategies such as genetic therapies and cell therapy as well as accelerated development of pharmaceutical drugs and mutation-specific therapies. The frequent introduction of exon skipping technology and advancements in genetic studies further bolster this growing trend.
The escalating prevalence of Duchenne muscular dystrophy (DMD), a genetic disorder that obstructs the production of an essential muscle protein, dystrophin, leading to progressive muscle deterioration, is set to stimulate the growth of the Elevidys market. The increase in DMD cases is primarily linked to enhanced awareness and diagnostics abilities, leading to earlier and more accurate identification of the condition. Using a micro-dystrophin gene, Elevidys works to treat DMD by providing partial restoration of the dystrophin protein function in muscle cells. For example, Murdoch Children’s Research Institute, a child health research center based in Australia, revealed in December 2023 that approximately 1,000 individuals in Australia are impacted by DMD. This surge in the prevalence of Duchenne muscular dystrophy is projected to propel the Elevidys market's expansion.
The elevidys market covered in this report is segmented –
1) By Clinical Indication: Duchenne Muscular Dystrophy, Other Indications
2) By Distribution Channel: Specialty Pharmacies, Hospitals, Clinics
3) By End-User: Research Institutions, Homecare Settings
The chief trend in the elevidys market is centered around the creation of inventive drug solutions, including gene therapy, to facilitate early detection and personalized treatment strategies for patients with Duchenne muscular dystrophy. The use of gene therapy for the treatment of Duchenne muscular dystrophy (DMD) represents a revolutionary medical strategy designed to tackle the fundamental genetic reason of DMD by introducing a working copy of the dystrophin gene or its microdystrophin variant into the muscle cells. For example, in June 2023, US-based Sarepta Therapeutics Inc., a company dedicated to medical research and the development of drugs, revealed that they had secured approval from the Food and Drug Administration for Elevidys (delandistrogene moxeparvovec-rokl), paving the way as the pioneering gene therapy for Duchenne muscular dystrophy (DMD). This endorsement is for ambulatory pediatric patients between the ages of 4 to 5 years diagnosed with a verified DMD gene mutation.
Major companies operating in the elevidys market include:
• Sarepta Therapeutics Inc.
North America was the largest region in the elevidys market in 2024. Asia-Pacific is expected to be the fastest-growing region in the forecast period. The regions covered in the elevidys market report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East and Africa.