Drug intelligence / Profile preview

olaptesed pegol + pembrolizumab

Development stage
Unknown
Lead developer
TME Pharma
Modality
RNA Aptamers → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics, DNA Aptamers → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

Olaptesed pegol (NOX-A12) is a PEGylated L-stereoisomer RNA aptamer that acts as an antagonist of the chemokine CXCL12 (also known as SDF-1). It disrupts the interaction between CXCL12 and its receptors, thereby modulating the tumor microenvironment to enhance immune cell infiltration and sensitize tumors to immunotherapy. Pembrolizumab is a monoclonal antibody targeting PD-1, blocking its interaction with PD-L1/PD-L2, thus promoting T-cell mediated anti-tumor responses. The combination of olaptesed pegol and pembrolizumab is being investigated in clinical trials for treatment-refractory solid tumors such as metastatic colorectal cancer and glioblastoma, aiming to synergistically improve anti-tumor immunity by both disrupting immune evasion mechanisms in the tumor microenvironment (via CXCL12 inhibition) and releasing T-cell inhibition (via PD-1 blockade)[5][6][7].

Other names
olaptesed pegol + KeytrudaNOX-A12 + pembrolizumab
02

Targets

CXCL12 (C-X-C motif chemokine ligand 12)PDCD1 (Programmed cell death protein 1 receptor)

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