Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
rG47-PRS1 is an engineered oncolytic herpes simplex virus (oHSV) derived from the G47Δ backbone, specifically designed for the treatment of PAX3-FOXO1 (P3F) positive alveolar rhabdomyosarcoma (aRMS). The virus incorporates a synthetic P3F-responsive promoter—constructed from a PRS1 element and a minimal Myogenin promoter—to drive the expression of the cytotoxic ICP34.5 gene. This mechanism ensures that viral replication and subsequent tumor cell lysis occur selectively in cells expressing the PAX3-FOXO1 fusion protein. Preclinical studies demonstrate that rG47-PRS1 not only exhibits direct cytotoxicity but also activates the NF-kB pathway and enhances the infiltration of CD45+ lymphocytes, thereby sensitizing immunologically cold aRMS tumors to immune checkpoint inhibitors like anti-PD1 antibodies.
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 rG47-PRS1.