Drug intelligence / Profile preview

BPI-572270

Development stage
Phase 2
Lead developer
Betta Pharmaceuticals
Modality
Small Molecules
Administration
Oral
01

Overview

BPI-572270 is an investigational, orally bioavailable small molecule inhibitor developed by Betta Pharmaceuticals that specifically targets the KRAS G12D mutation. KRAS G12D is a frequent driver mutation in several aggressive cancers, including pancreatic ductal adenocarcinoma (PDAC), colorectal cancer (CRC), and non-small cell lung cancer (NSCLC). By selectively binding to the KRAS G12D protein, BPI-572270 inhibits the constitutive activation of the RAS signaling pathway, thereby blocking downstream cascades like RAF-MEK-ERK that are essential for tumor cell proliferation and survival. The drug is currently being evaluated in Phase 1/2 clinical trials to determine its safety, tolerability, and preliminary efficacy in patients with advanced solid tumors harboring the KRAS G12D mutation.

02

Targets

KRASG12D (Kirsten rat sarcoma viral oncogene homolog (KRAS) G12D mutant)

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