Literature DB >> 16597200

Miltefosine: oral treatment of leishmaniasis.

Jaime Soto1, Paula Soto.   

Abstract

The well-known problems of classic treatment of the leishmaniases with pentavalent antimony (reduced efficacy), difficulties of administration and increasing frequency and severity of adverse events have stimulated the search for new drugs to treat these diseases. Other injectable, oral and topical drugs have not been consistently effective, especially in the modern World. Beginning in 1998, Indian researchers conducted several trials with hexadecylphosphocholine (miltefosine) in patients with visceral leishmaniasis, and in 1999, clinical studies were initiated in Colombia for cutaneous disease. More than 2500 patients have been treated, including patients with diffuse cutaneous leishmaniasis, mucosal disease and patients coinfected with HIV. Cure rates between 91 and 100% were reached with a dose of 2.5 mg/kg/day for 28 days, with no difference between treatment-naive and relapsing patients. Mild gastrointestinal events were present in 35-60% of patients and 10-20% had mild transaminase and creatinine elevations. Miltefosine has potent leishmanicidal activity as a consequence of its interference in parasite metabolic pathways and the induction of apoptosis. Miltefosine is the first effective and safe oral agent with the potential to treat all major clinical presentations of leishmaniasis.

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Year:  2006        PMID: 16597200     DOI: 10.1586/14787210.4.2.177

Source DB:  PubMed          Journal:  Expert Rev Anti Infect Ther        ISSN: 1478-7210            Impact factor:   5.091


  14 in total

1.  Miltefosine efficiently eliminates Leishmania major amastigotes from infected murine dendritic cells without altering their immune functions.

Authors:  Klaus Griewank; Caroline Gazeau; Andreas Eichhorn; Esther von Stebut
Journal:  Antimicrob Agents Chemother       Date:  2009-12-07       Impact factor: 5.191

2.  [Cutaneous leishmaniasis--an import from Belize].

Authors:  Jakob Schnedl; Herbert Auer; Marcellus Fischer; Herbert Tomaso; Tom Pustelnik; Gerhard Mooseder
Journal:  Wien Klin Wochenschr       Date:  2007       Impact factor: 1.704

3.  Agonist potency at P2X7 receptors is modulated by structurally diverse lipids.

Authors:  A D Michel; E Fonfria
Journal:  Br J Pharmacol       Date:  2007-08-13       Impact factor: 8.739

4.  Broad Spectrum and Safety of Oral Treatment with a Promising Nitrosylated Chalcone in Murine Leishmaniasis.

Authors:  Ariane J Sousa-Batista; Douglas Escrivani-Oliveira; Camila Alves Bandeira Falcão; Cintia Iana Monteiro da Silva Philipon; Bartira Rossi-Bergmann
Journal:  Antimicrob Agents Chemother       Date:  2018-09-24       Impact factor: 5.191

5.  Leishmania (Viannia) panamensis: an in vitro assay using the expression of GFP for screening of antileishmanial drug.

Authors:  Rubén E Varela M; Diana Lorena Muñoz; Sara M Robledo; Bala K Kolli; Sujoy Dutta; Kwang Poo Chang; Carlos Muskus
Journal:  Exp Parasitol       Date:  2009-03-20       Impact factor: 2.011

6.  Successful treatment of multifocal cutaneous leishmaniasis with miltefosine.

Authors:  Bhushan Madke; Vidya Kharkar; Siddhi Chikhalkar; Sunanda Mahajan; Uday Khopkar
Journal:  Indian J Dermatol       Date:  2011 Sep-Oct       Impact factor: 1.494

7.  Comparison of cardiotoxicity between N-methyl-glucamine and miltefosine in the treatment of American cutaneous leishmaniasis.

Authors:  Daniel Holanda Barroso; Ciro Martins Gomes; Antônia Marilene da Silva; Raimunda Nonata Ribeiro Sampaio
Journal:  An Bras Dermatol       Date:  2021-05-15       Impact factor: 1.896

8.  Miltefosine in the treatment of leishmaniasis: Clinical evidence for informed clinical risk management.

Authors:  Shyam Sundar; Piero L Olliaro
Journal:  Ther Clin Risk Manag       Date:  2007-10       Impact factor: 2.423

9.  The impact of human immunodeficiency virus (HIV) co-infection on the economic burden of cutaneous leishmaniasis (CL) in Brazil and potential value of new CL drug treatments.

Authors:  Stephanie D Kruchten; Kristina M Bacon; Bruce Y Lee
Journal:  Am J Trop Med Hyg       Date:  2014-07-07       Impact factor: 2.345

10.  The Qi Site of Cytochrome b is a Promiscuous Drug Target in Trypanosoma cruzi and Leishmania donovani.

Authors:  Richard J Wall; Sandra Carvalho; Rachel Milne; Juan A Bueren-Calabuig; Sonia Moniz; Juan Cantizani-Perez; Lorna MacLean; Albane Kessler; Ignacio Cotillo; Lalitha Sastry; Sujatha Manthri; Stephen Patterson; Fabio Zuccotto; Stephen Thompson; Julio Martin; Maria Marco; Timothy J Miles; Manu De Rycker; Michael G Thomas; Alan H Fairlamb; Ian H Gilbert; Susan Wyllie
Journal:  ACS Infect Dis       Date:  2020-01-30       Impact factor: 5.084

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