Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ERAS-601 + pembrolizumab is an investigational combination therapy under clinical evaluation for advanced or metastatic solid tumors. ERAS-601 is a potent, selective, orally bioavailable allosteric inhibitor of SHP2 (encoded by PTPN11), a protein tyrosine phosphatase critical for signaling downstream of multiple receptor tyrosine kinases, including the RAS/MAPK pathway. Pembrolizumab is a well-established, FDA-approved monoclonal antibody and immune checkpoint inhibitor targeting programmed cell death protein 1 (PD-1), thereby enhancing antitumor immune response. The combination aims to simultaneously inhibit tumor growth signaling and reinvigorate immune responses against cancer cells. Early-phase trials are focused on safety, tolerability, optimal dosing, and preliminary efficacy in advanced or metastatic solid tumors[3][5].
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 ERAS-601 + pembrolizumab.