Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
GEC255 is an orally bioavailable small molecule inhibitor that selectively targets the oncogenic Kirsten rat sarcoma viral oncogene homolog (KRAS) G12C mutation, a driver of tumorigenesis in several cancers. By binding to and inhibiting the mutant KRAS G12C protein, GEC255 blocks downstream signaling pathways involved in cell proliferation and survival. It has demonstrated promising antitumor activity in advanced non-small cell lung cancer (NSCLC) patients harboring the KRAS G12C mutation, including those who have failed prior therapies. In Phase 1 clinical trials, it showed high selectivity for its target with favorable safety and pharmacokinetic profiles; most adverse events were mild or moderate (grade 1 or 2), such as diarrhea, elevated ALT, rash, and anemia. The drug is being developed by GenEros Biopharma[1][3][4][6][7].
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 GEC255.