Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
RMD1307 is an investigational gene therapy being developed by Remedium Bio for the treatment of sarcopenia, a condition characterized by age-related muscle loss and decline in physical function. The therapy utilizes the company's proprietary 'Prometheus' platform to deliver the follistatin (FST) gene, which encodes a protein that serves as a potent inhibitor of myostatin (GDF-8) and other members of the transforming growth factor-beta (TGF-β) superfamily that negatively regulate muscle mass. By overexpressing follistatin, RMD1307 aims to promote muscle hypertrophy, increase strength, and restore mobility. The program is designed for delivery via either adeno-associated virus (AAV) vectors or lipid nanoparticles (LNPs). As of 2024, RMD1307 is in the IND-enabling stage of development.
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 RMD1307.