Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
A combination of **bedaquiline** and **delamanid**, two oral small-molecule antimycobacterial drugs, is used as part of salvage or individualized regimens for multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis. **Bedaquiline** inhibits mycobacterial ATP synthase, thereby blocking energy generation in *Mycobacterium tuberculosis*. **Delamanid** is a prodrug activated by the mycobacterial F420 coenzyme system, where it inhibits synthesis of methoxy- and keto-mycolic acids, critical for the mycobacterial cell wall, and generates reactive nitrogen species. The combination is considered when therapy options are limited and there is extensive drug resistance, but carries an increased risk of QT interval prolongation. Large studies and limited clinical reports suggest this combination may be justified in select patients with careful cardiac monitoring[1][3].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on bedaquiline + delamanid.