Drug intelligence / Profile preview

bemnifosbuvir + buprenorphine + naloxone + ruzasvir

Development stage
Unknown
Lead developer
Atea Pharmaceuticals
Modality
Small Molecules
Administration
Oral, Sublingual
01

Overview

Buprenorphine + naloxone + BEM + RZR is an investigational drug combination being studied for the treatment of chronic Hepatitis C Virus (HCV) infection in patients receiving opioid maintenance therapy. The regimen consists of bemnifosbuvir (BEM, AT-527), an oral nucleotide analog polymerase inhibitor targeting the HCV NS5B polymerase, and ruzasvir (RZR, AT-038), an oral NS5A inhibitor. These antivirals are co-administered with buprenorphine and naloxone, which are standard-of-care medications for opioid use disorder. Developed by Atea Pharmaceuticals, this combination is specifically evaluated in Phase 1 drug-drug interaction (DDI) trials to assess the pharmacokinetic compatibility of the BEM/RZR pan-genotypic HCV regimen with stable opiate maintenance therapy, facilitating the inclusion of this high-prevalence patient population in late-stage clinical trials.

Other names
BEM/RZR + buprenorphine/naloxonebemnifosbuvir + ruzasvir + buprenorphine + naloxone
02

Targets

MOR (Mu opioid receptor)KOR (Kappa opioid receptor)DOR (Opioid Receptor Delta 1)NS5B (Hepatitis C virus non-structural protein 5B (NS5B) RNA-dependent RNA polymerase)NS5A (Hepatitis C virus nonstructural protein 5A (genotype 1b))

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