Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
HYP-DMD-01 is an investigational allogeneic cell therapy composed of mesenchymal stem cells (MSCs) derived from the umbilical cord lining (ULSCs). Developed by RESTEM LLC in collaboration with the University of Florida College of Medicine, the therapy is currently in Phase 1 clinical development for the treatment of Duchenne Muscular Dystrophy (DMD). The mechanism of action involves the systemic administration of these stem cells, which are hypothesized to migrate to damaged muscle tissue and exert immunomodulatory and regenerative effects. By secreting various trophic factors and cytokines, the cells aim to reduce chronic inflammation, decrease muscle fibrosis, and promote the repair of dystrophic muscle fibers, potentially slowing the progression of the disease and improving muscle function. The program is supported by the philanthropic organization JAR of Hope.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on HYP-DMD-01.