Drug intelligence / Profile preview

QLF31911

Development stage
Unknown
Lead developer
Qilu Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

QLF31911 is an investigational, orally bioavailable small molecule inhibitor developed by Qilu Pharmaceutical that specifically targets the KRAS G12D mutation. KRAS G12D is a prominent oncogenic driver found in a significant proportion of pancreatic, colorectal, and non-small cell lung cancers. By selectively binding to the G12D mutant form of the KRas protein, QLF31911 prevents the protein from activating downstream signaling pathways, such as the MAPK/ERK and PI3K/AKT pathways, which are essential for tumor cell growth and survival. Unlike KRAS G12C inhibitors that utilize covalent bonding, KRAS G12D inhibitors typically function through high-affinity non-covalent binding to lock the protein in its inactive GDP-bound state. The drug is currently being evaluated in Phase 1 clinical trials for patients with advanced malignant tumors harboring the KRAS G12D mutation.

02

Targets

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

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