Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Pentavalent antimony (Sbv) is a parenteral antimonial compound used as a standard treatment for cutaneous leishmaniasis. It is typically administered at a dose of 15-20mg/kg per day for 20 days. Despite being a standard treatment, it faces challenges such as therapeutic failure in up to 50% of patients, a prolonged healing period of 60 to 90 days for ulcerated lesions, and the parenteral route of administration which can hinder patient adherence, particularly in rural settings. Research has explored its use in combination with other agents, such as GM-CSF, to potentially improve cure rates, and with topical rSm29 functionalized onto gold nanoparticles to reduce inflammation and parasite load in experimental models.
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 Pentavalent antimony.