For over two decades, Parent Project Muscular Dystrophy has been committed to exploring and supporting every single therapeutic possibility. We take a cutting-edge approach to accelerate finding treatments that will end Duchenne for every single person impacted by the disease. The therapeutic pipeline of potential treatments for Duchenne has never been so full of promise. And it’s never been more important to ensure that the path to progress is clear, so that safe and effective therapies can reach the people who need them quickly and affordably.
In this section, PPMD outlines our ambitious research strategy, takes a deeper dive into the numerous therapeutic approaches being explored, helps you and your family navigate the complex world of clinical trials, and introduces you to what’s next in Duchenne research.