Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Meglumine antimoniate is a pentavalent antimonial compound that serves as a cornerstone in the treatment of leishmaniasis, a parasitic disease caused by species of the genus *Leishmania*. It is primarily indicated for visceral, cutaneous, and mucocutaneous leishmaniasis. The drug acts as a prodrug, undergoing reduction to the more toxic trivalent antimony (SbIII) within the parasite or host cells. This active form disrupts the parasite's energy metabolism by inhibiting glycolysis and fatty acid oxidation, and it interferes with the thiol-based redox system by inhibiting trypanothione reductase, leading to oxidative stress and parasite death. While effective, its use is associated with significant side effects, including cardiotoxicity, pancreatitis, and nephrotoxicity, and it requires parenteral administration, typically via intramuscular or intralesional routes.
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 meglumine antimoniate.