Drug intelligence / Profile preview

RMC-0708

Development stage
Preclinical
Lead developer
REVOLUTION Medicines
Modality
Small Molecules
Administration
Oral
01

Overview

RMC-0708 (also known as RM-046) is a first-in-class, oral, small molecule inhibitor that selectively targets the KRASQ61H(ON) mutant protein. It is designed to drive tumor regression by inhibiting the active (GTP-bound or "ON") state of KRAS Q61H—a mutation implicated in various cancers. The drug acts as a non-covalent, mutant-selective tri-complex inhibitor and has demonstrated robust anti-tumor activity in preclinical models. Developed by Revolution Medicines, RMC-0708 validates KRASQ61H as a therapeutic target and represents an innovative approach for treating cancers driven by this specific mutation[1][2][3][9].

Other names
RMC-0708RMC0708RMC 0708RM-046RM046RM 046
02

Targets

KRAS Q61H (Kirsten rat sarcoma viral oncogene homolog Q61H mutant)

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