Drug intelligence / Profile preview

BPaQ

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

Overview

BPaQ is an investigational combination anti-tuberculosis regimen consisting of bedaquiline, pretomanid, and quabodepistat (OPC-167832). Developed by Otsuka Pharmaceutical, the regimen is designed to treat rifampicin-resistant (RR-TB) and multidrug-resistant tuberculosis (MDR-TB). Quabodepistat is a novel carbostyril derivative that acts as a potent inhibitor of decaprenylphosphoryl-β-D-ribose-2'-oxidase (DprE1), an essential enzyme for Mycobacterium tuberculosis to synthesize the cell wall component arabinogalactan. Bedaquiline inhibits mycobacterial ATP synthase, disrupting energy production, while pretomanid is a nitroimidazole that inhibits mycolic acid synthesis and causes respiratory poisoning in the bacteria. The regimen is currently being evaluated in the Phase 3 QUANTUM-TB trial to determine if it can shorten treatment duration to 4 or 6 months compared to the current standard of care.

Other names
Bedaquiline + Pretomanid + Quabodepistat
02

Targets

DendrinAtpE (Mycobacterium tuberculosis ATP synthase subunit c)DprE1 (Decaprenylphosphoryl-beta-D-ribose oxidase)

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