Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Pifazimine (B4154) is a riminophenazine derivative and a structural analogue of clofazimine, specifically developed for the treatment of multidrug-resistant tuberculosis (MDR-TB). Developed by the Institute of Medicinal Biotechnology of the Chinese Academy of Medical Sciences in collaboration with Beijing Xiehe Pharmaceutical Factory No. 2, pifazimine aims to provide a more potent and less toxic alternative to clofazimine, particularly by reducing the severe skin pigmentation side effects associated with the latter. Its mechanism of action involves the disruption of the mycobacterial respiratory chain; the drug is reduced by the bacterial NADH dehydrogenase (NDH-2), which subsequently leads to the generation of lethal reactive oxygen species (ROS) within the cell. Additionally, it may interfere with bacterial membrane function and bind to mycobacterial DNA. Clinical development has primarily focused on its inclusion in combination regimens for drug-resistant strains of *Mycobacterium tuberculosis*.
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 pifazimine.