Drug intelligence / Profile preview

AVP-786

Development stage
Unknown
Lead developer
Otsuka Pharmaceutical Development & Commercialization
Modality
Small Molecules
Administration
Oral
01

Overview

AVP-786 is an investigational small molecule combination therapy consisting of deudextromethorphan hydrobromide (a deuterated form of dextromethorphan) and quinidine sulfate. It is designed as a second-generation successor to Nuedexta (AVP-923). Deudextromethorphan acts as a sigma-1 receptor agonist and an uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist, while quinidine serves as a potent inhibitor of the CYP2D6 enzyme to increase the systemic exposure of the dextromethorphan component. The drug was primarily developed by Avanir Pharmaceuticals (acquired by Otsuka) in collaboration with Concert Pharmaceuticals. It has been evaluated for several neuropsychiatric conditions, including agitation in Alzheimer's disease, schizophrenia, and Intermittent Explosive Disorder (IED). However, the Phase 2 trial for IED was terminated due to recruitment difficulties, and the Phase 3 program for Alzheimer's agitation was discontinued in 2024 after failing to meet primary endpoints.

Other names
Deudextromethorphan hydrobromide + quinidine sulfated6-DM/QDeudextromethorphan + quinidine
02

Targets

SERT (Sodium-dependent serotonin transporter)SIGMAR1 (Sigma non-opioid intracellular receptor 1)NMDAR (Glutamate receptor ionotropic, NMDA)NET (Norepinephrine Transporter)

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