Drug intelligence / Profile preview

NOX-B11-2

Development stage
Preclinical
Lead developer
TME Pharma
Modality
MicroRNA (miRNA) → Small 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, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Spiegelmers → RNA Aptamers → RNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous, Intravenous
01

Overview

NOX-B11-2 is a Spiegelmer—a synthetic L-RNA oligonucleotide designed to bind and neutralize the peptide hormone ghrelin. Ghrelin is the endogenous ligand of the growth hormone secretagogue receptor 1a and is a key regulator of growth hormone release, appetite, and adiposity. NOX-B11-2 binds specifically to ghrelin, preventing its interaction with its receptor and thereby blocking ghrelin-induced food intake and neuronal activation in the arcuate nucleus. Preclinical studies show that NOX-B11-2 decreases food intake, reduces body weight, and fat mass in rodent models of obesity by neutralizing circulating ghrelin. The drug is administered subcutaneously and acts peripherally; it does not penetrate the central nervous system. The approach is under investigation as a potential therapy for obesity and conditions associated with hyperghrelinemia, such as Prader-Willi syndrome[3][4][5][7][9].

Other names
Spiegelmer NOX-B11-2anti-ghrelin Spiegelmer
02

Targets

GHSR (Growth hormone secretagogue receptor)

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