Anti-leishmanial Drug Discovery: Rising to the Challenges of a Highly Neglected Disease

Table 2

Anti-leishmanial Treatments

Drug Primary Use Comments
Pentavalent antimony (sodium stibogluconate, meglumine antimoniate) Cutaneous, Muco-cutaneous, Visceral Adverse effects include cardiotoxicity, pain, nausea. Will no longer be manufactured by GlaxoSmith Kline, UK after 2012.
Amphotericin B formulations (polyene antibiotic) Muco-cutaneous, Visceral, Cutaneous Impacts cell membrane integrity. No known MOA. Adverse effects include painful administration, anemia, hypokalemia, renal toxicity. Multiple formulations.
Pentamidine (diamidine) Cutaneous, Muco-cutaneous, Visceral No known MOA. Rare adverse effects but include pain, nausea, vomiting.
Fluconazole Cutaneous Effects ergosterol biosynthesis. Rare adverse effects but include pain, nausea, diarrhea.
Itracanazole Cutaneous Effects ergosterol biosynthesis. Adverse effects include pain, nausea, diarrhea.
Allopurinol Cutaneous Inhibits xanthine oxidase. Adverse effects include pain, nausea, rash, diarrhea.
Paromomycin (aminosidine, monomycin) Visceral, Cutaneous Impacts protein synthesis. Adverse effects include pain, nausea, diarrhea, liver toxicity, erythema, mild edema.
Ketoconazole Cutaneous Effects ergosterol biosynthesis. Adverse effects include hepatotoxicity, endocrine dysfunction.
Miltefosine (hexadecylphosphocholine) Visceral Impacts cell membrane integrity. No known MOA. Adverse effects include nausea, vomiting, diarrhea.
  • MOA, mechanism of action.

This Article

  1. MI April 2010 vol. 10 no. 2 72-75