Drug intelligence / Profile preview

mavoglurant

Development stage
Phase 3
Lead developer
STALICLA
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Mavoglurant is an investigational small molecule drug that acts as a selective negative allosteric modulator (antagonist) of the metabotropic glutamate receptor 5 (mGluR5). It was originally developed by Novartis and has been studied for several neuropsychiatric and neurological conditions, including fragile X syndrome, Parkinson's disease (specifically levodopa-induced dyskinesia), obsessive-compulsive disorder (OCD), alcohol use disorder, cocaine use disorder, Huntington's disease chorea, anxiety disorders, gastroesophageal reflux disease (GERD), and smoking withdrawal. Mavoglurant reached phase II/III clinical trials in some indications but failed to demonstrate efficacy in pivotal studies for fragile X syndrome and levodopa-induced dyskinesia. Development for these indications was discontinued by Novartis. More recently, Stalicla acquired rights to the drug from Novartis to pursue development in substance-use disorders and neurodevelopmental disorders[3][4][5][6][9].

Other names
543906-09-8mavoglurant [INN]
02

Targets

GRM5 (Metabotropic glutamate receptor 5)

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