Drug intelligence / Profile preview

bedaquiline + delamanid + linezolid + moxifloxacin + pyrazinamide

Development stage
Unknown
Lead developer
Shenzhen Third People's Hospital
Modality
Small Molecules
Administration
Oral
01

Overview

This is a five-drug oral combination regimen specifically investigated for the treatment of rifampicin-resistant tuberculosis (RR-TB). Developed and evaluated in clinical trials by the Shenzhen Third People's Hospital, the regimen consists of bedaquiline, delamanid, linezolid, moxifloxacin, and pyrazinamide. Bedaquiline acts by inhibiting mycobacterial ATP synthase, while delamanid interferes with mycolic acid synthesis. Linezolid provides protein synthesis inhibition via the 50S ribosome, moxifloxacin targets DNA gyrase to prevent bacterial replication, and pyrazinamide is thought to disrupt mycobacterial cell membrane functions. This combination is part of a broader effort to create shortened, all-oral, and highly effective treatments for drug-resistant tuberculosis, reducing the burden of long-term injectable-based therapies.

Other names
BDeLMPy regimenShenzhen regimen
02

Targets

23S rRNA (23S ribosomal RNA)AtpE (ATP synthase subunit c of Mycobacterium tuberculosis)DNA gyraseMmpL3 (Mycobacterial membrane protein Large 3)

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