Drug intelligence / Profile preview

NiKang KRAS G12D inhibitor

Development stage
Preclinical
Lead developer
NiKang Therapeutics
Modality
Small Molecules
Administration
Oral
01

Overview

NiKang KRAS G12D inhibitor is a preclinical small molecule designed to selectively target and inhibit the KRAS G12D oncogenic mutant. KRAS G12D is a frequent driver mutation in several aggressive malignancies, including pancreatic cancer, colorectal cancer, and lung adenocarcinoma. By binding to the G12D mutant form of the KRAS protein, the inhibitor blocks the constitutive activation of downstream signaling pathways, such as MAPK/ERK and PI3K/AKT, which are essential for tumor cell proliferation and survival. Developed by NiKang Therapeutics, this compound aims to provide a targeted therapeutic option for patients with solid tumors harboring this specific genetic alteration.

Other names
KRAS G12D inhibitor
02

Targets

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

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