Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This SOS1 inhibitor is a small molecule therapeutic being developed by Acerand Therapeutics for the treatment of solid tumors. It specifically targets Son of Sevenless homolog 1 (SOS1), a guanine nucleotide exchange factor (GEF) that plays a critical role in the activation of RAS proteins. By binding to SOS1, the inhibitor prevents the exchange of guanosine diphosphate (GDP) for guanosine triphosphate (GTP) on RAS, thereby maintaining RAS in its inactive state and blocking downstream oncogenic signaling through the MAPK/ERK pathway. This mechanism is designed to address cancers driven by various RAS mutations, including KRAS G12D, either as a monotherapy or in combination with direct RAS inhibitors to overcome resistance. The drug is currently in the IND-enabling phase 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 SOS1 inhibitor (Acerand Therapeutics).