PUBLISHER: Global Market Insights Inc. | PRODUCT CODE: 1544647
PUBLISHER: Global Market Insights Inc. | PRODUCT CODE: 1544647
Duchenne Muscular Dystrophy Drugs Market size is projected to expand at an 11.6% CAGR from 2024 to 2032, led by the rising government and regulatory support along with increasing R and D efforts. Governments are expediting the availability of new treatments for duchenne muscular dystrophy (DMD) through funding and regulatory approvals. Researchers are innovating therapies and enhancing existing drugs to meet the needs of DMD patients. For instance, in March 2024, the U.S. FDA nodded Duvyzat (givinostat), an oral treatment for DMD, for patients aged six years and older.
The overall market is segregated into drug type, route of administration, and region.
Based on drug type, the DMD drugs market value from the gene therapy segment is estimated to grow at a significant rate from 2024 to 2032, driven by the urgent need to tackle the condition's genetic root. Gene therapies aim to correct or replace the faulty dystrophin gene, pivotal in muscle degeneration. Researchers are directly delivering functional dystrophin gene copies to muscle cells, employing advanced vectors for optimal gene transfer and expression.
Duchenne muscular dystrophy drugs industry from the injectable route of administration segment is anticipated to grow at a substantial CAGR through 2032 fueled by the rising demand for effective treatment delivery. Injectables offer direct access to muscle tissue or systemic circulation, enhancing drug absorption and efficacy. Moreover, advancements in injectable technologies are paving the way for efficient delivery systems, including sustained-release formulations and novel delivery methods.
Regionally, the Asia Pacific duchenne muscular dystrophy drugs market size is projected to witness a notable CAGR between 2024 and 2032, on account of the increasing collaborations among pharmaceutical companies, research institutions, and biotech firms. These partnerships, spanning clinical trials, drug development, and regulatory support, are set to enhance therapeutic options and outcomes for DMD patients in the region.