Drug intelligence / Profile preview

D3S-001 + pembrolizumab

Development stage
Unknown
Lead developer
D3 Bio
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

A combination therapy of D3S-001, an orally administered, next-generation covalent KRAS G12C inhibitor designed for high potency and rapid engagement of the GDP-bound KRAS G12C mutant protein, and pembrolizumab, a monoclonal antibody immune checkpoint inhibitor targeting PD-1. This regimen is under investigation for advanced solid tumors (notably non-small cell lung cancer and colorectal cancer) harboring KRAS p.G12C mutations, particularly in patients resistant to first-generation KRAS G12C inhibitors. D3S-001 provides robust inhibition of KRAS G12C irrespective of nucleotide cycling and is intended to be synergistic with pembrolizumab’s immune-modulating activity. D3S-001 is being developed by D3 Bio, while pembrolizumab is developed and manufactured by Merck. The combination is investigational and administered with D3S-001 orally and pembrolizumab intravenously, as part of ongoing Phase 1/2 clinical trials[1][2][3][4][5][6][7][9][10].

Brand names
Keytruda
Other names
D3S-001 + Keytruda
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)KRASG12C (Kirsten rat sarcoma viral oncogene homolog G12C)

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