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Miltefosine (Impavido): the first oral treatment against leishmaniasis
Authors:H.?Sindermann,S.?L.?Croft,K.?R.?Engel,W.?Bommer,H.?J.?Eibl,C.?Unger,J.?Engel  author-information"  >  author-information__contact u-icon-before"  >  mailto:Juergen.engel@zentaris.de"   title="  Juergen.engel@zentaris.de"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Zentaris AG, Weismüllerstrasse 45, 60314 Frankfurt am Main, Germany;(2) London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK;(3) Georg-August-University of Göttingen, Institute of Hygiene, Windausweg 2, 37073 Göttingen, Germany;(4) Max-Planck-Institut für Biophysikalische Chemie, Am Fassberg, 37077 Göttingen, Germany;(5) Klinik für Tumorbiologie, Breisacher Strasse 117, 79106 Freiburg, Germany
Abstract:Miltefosine is a novel antileishmanial drug that has significant selectivity in both in vitro and in vivo models. Clinical efficacy was demonstrated for the treatment of visceral leishmaniasis with the advantage of oral administration over the currently recommended antileishmanial drugs that require parenteral administration. Miltefosine produces high cure rates also in patients resistant to the standard antimonial therapy.
Keywords:Visceral leishmaniasis  Miltefosine  Oral activity  Antimonial resistance
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