Drug intelligence / Profile preview

emapticap pegol

Development stage
Phase 2
Lead developer
TME Pharma
Modality
RNA Aptamers → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, DNA Aptamers → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous, Subconjunctival
01

Overview

Emapticap pegol (NOX-E36) is an injectable PEGylated L-stereoisomer RNA aptamer, also known as a Spiegelmer, that specifically binds and neutralizes the human chemokine CCL2 (C-C motif ligand 2, also called monocyte chemoattractant protein-1 or MCP-1), as well as three highly related chemokines. By inhibiting CCL2, NOX-E36 blocks the recruitment and differentiation of inflammatory cells such as monocytes/macrophages mediated by MCP-1. This mechanism targets key pathways involved in inflammation and fibrosis. Emapticap pegol has completed Phase 1 and Phase 2 clinical studies in over 100 subjects for diabetic nephropathy, demonstrating safety, tolerability, and dose-dependent targeting of macrophages. More recently, it is being developed for ophthalmology indications such as glaucoma filtration surgery to prevent post-surgical fibrosis with a favorable safety profile compared to current standards like mitomycin C. The drug was originally developed by TME Pharma (formerly Noxxon Pharma) with ongoing collaborations including the Singapore Eye Research Institute[1][3][5][6].

Other names
emapticap pegol
02

Targets

CCL2 (C-C motif chemokine 2)

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