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BE-PEP Bedaquiline
Bedaquiline inhibits bacterial ATP synthase, disrupting energy production in Mycobacterium tuberculosis.
Bedaquiline inhibits bacterial ATP synthase, disrupting energy production in Mycobacterium tuberculosis. Used for Multidrug-resistant tuberculosis (MDR-TB), Extensively drug-resistant tuberculosis (XDR-TB).
At a glance
| Generic name | BE-PEP Bedaquiline |
|---|---|
| Sponsor | Institute of Tropical Medicine, Belgium |
| Drug class | ATP synthase inhibitor |
| Target | Mycobacterial ATP synthase |
| Modality | Small molecule |
| Therapeutic area | Infectious Disease |
| Phase | Phase 3 |
Mechanism of action
Bedaquiline is a diarylquinoline that binds to the ATP synthase enzyme of tuberculosis bacteria, blocking ATP synthesis and causing rapid bactericidal activity. This mechanism is distinct from existing TB drugs and is effective against both drug-susceptible and multidrug-resistant tuberculosis strains. BE-PEP likely refers to a bedaquiline-containing combination regimen being evaluated in Phase 3 trials.
Approved indications
- Multidrug-resistant tuberculosis (MDR-TB)
- Extensively drug-resistant tuberculosis (XDR-TB)
Common side effects
- QT prolongation
- Hepatotoxicity
- Peripheral neuropathy
- Gastrointestinal disturbances
Key clinical trials
- Bedaquiline Enhanced Post ExpOsure Prophylaxis for Leprosy (Phase 2) (PHASE2)
- Bedaquiline Enhanced Post ExpOsure Prophylaxis for Leprosy (PHASE3)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- BE-PEP Bedaquiline CI brief — competitive landscape report
- BE-PEP Bedaquiline updates RSS · CI watch RSS
- Institute of Tropical Medicine, Belgium portfolio CI