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Amphotericin B lipid complex: in visceral leishmaniasis
David R Goldsmith1, Caroline M Perry
1Adis International Limited, Auckland, New Zealand. demail@adis.co.nz
Drugs
|August 27, 2004
Summary
Amphotericin B lipid complex offers high cure rates for visceral leishmaniasis (VL), even in antimonial-resistant cases. This antifungal drug formulation is well-tolerated, with infusion reactions being the most common side effect.
Area of Science:
- Infectious Diseases
- Pharmacology
- Tropical Medicine
Background:
- Visceral leishmaniasis (VL) is a serious parasitic disease.
- Antimonial drugs are a common treatment for VL, but resistance is increasing.
- Amphotericin B lipid complex (ABLC) is a lipid formulation of amphotericin B, an antifungal with activity against Leishmania spp.
Purpose of the Study:
- To evaluate the efficacy and tolerability of ABLC in patients with VL.
- To compare ABLC with other amphotericin B formulations and standard treatments.
Main Methods:
- Randomised, open-label, dose-ranging studies were conducted.
- Short-course, once-daily intravenous infusions of ABLC were administered.
- Studies included patients with antimonial-resistant VL, previously untreated VL, and HIV-infected patients with VL.
Main Results:
- High rates of apparent (93-100%) and definitive (79-100%) cures were observed with ABLC in Indian patients with antimonial-resistant VL.
- ABLC demonstrated comparable efficacy to liposomal amphotericin B and conventional amphotericin B deoxycholate formulation in a mixed Indian population.
- In HIV-infected patients with VL, ABLC showed similar effectiveness to meglumine antimonate in a small pilot study in southern Europe.
- Infusion-related reactions were the most frequent adverse events associated with ABLC.
Conclusions:
- Short-course ABLC treatment is effective and well-tolerated for visceral leishmaniasis, including antimonial-resistant cases.
- ABLC represents a viable alternative treatment option for VL, particularly in resource-limited settings.
- Further research is warranted to explore ABLC's role in HIV-VL co-infection.