Drug intelligence / Profile preview

RP913

Development stage
Preclinical
Lead developer
Risen
Modality
PROTACs (E3 ligase recruitment) → Targeted Protein Degraders (TPDs) → Small Molecules, Bivalent/Multivalent Binders → Multivalent & Scaffold-Based Small Molecules → Small Molecules
01

Overview

RP913 is a proteolysis-targeting chimera (PROTAC) designed to induce the degradation of the KRAS G12D mutant protein. Developed by Risen Shanghai Medical Technology (Risen Pharma), it is currently in the IND-enabling stage for the treatment of various cancers driven by the KRAS G12D mutation. KRAS G12D is a common oncogenic driver in several solid tumors, including pancreatic, colorectal, and non-small cell lung cancers. By utilizing the PROTAC modality, RP913 aims to overcome the limitations of traditional small-molecule inhibitors by facilitating the ubiquitination and subsequent proteasomal degradation of the target protein, potentially offering more potent and durable therapeutic effects.

02

Targets

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

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