Drug intelligence / Profile preview

cosibelimab + olafertinib

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

Overview

Cosibelimab + olafertinib is a combination therapy being developed by Checkpoint Therapeutics for the treatment of non-small cell lung cancer (NSCLC). Cosibelimab (CK-301) is a high-affinity, fully human IgG1 monoclonal antibody that targets programmed death-ligand 1 (PD-L1). It blocks the interaction of PD-L1 with its receptors, PD-1 and B7.1, thereby restoring anti-tumor T-cell responses. Uniquely, cosibelimab features a functional Fc region designed to potentially induce antibody-dependent cellular cytotoxicity (ADCC), providing an additional mechanism of tumor cell clearance. Olafertinib (CK-101) is an oral, third-generation, irreversible small-molecule tyrosine kinase inhibitor (TKI) of the epidermal growth factor receptor (EGFR). It is designed to selectively target EGFR-sensitizing mutations and the T790M resistance mutation while sparing wild-type EGFR, which helps minimize off-target toxicities. The combination of these two agents is intended to provide a synergistic effect by simultaneously inhibiting oncogenic driver signaling and overcoming immune evasion in EGFR-mutated NSCLC.

Other names
cosibelimab and olafertinib combination
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)PDCD1 (Programmed cell death protein 1 receptor)CD274 (Programmed cell death protein 1 ligand 1)CD80 (T-lymphocyte activation antigen CD80)

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