Fosmidomycin-Clindamycin for Plasmodium falciparum Infections in African Children

Background. Fosmidomycin is a new antimalarial drug with a novel mechanism of action. Studies in Africa that have evaluated fosmidomycin as monotherapeutic agent demonstrated its excellent tolerance, but 3-timesdaily treatment regimens of ⩾4 days were required to achieve radical cure, prompting furt...

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Veröffentlicht in:The Journal of infectious diseases 2004-03, Vol.189 (5), p.901-908
Hauptverfasser: Borrmann, Steffen, Adegnika, Ayola A., Matsiegui, Pierre-Blaise, Issifou, Saadou, Schindler, Andreas, Mawili-Mboumba, Denise P., Baranek, Thomas, Wiesner, Jochen, Jomaa, Hassan, Kremsner, Peter G.
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container_issue 5
container_start_page 901
container_title The Journal of infectious diseases
container_volume 189
creator Borrmann, Steffen
Adegnika, Ayola A.
Matsiegui, Pierre-Blaise
Issifou, Saadou
Schindler, Andreas
Mawili-Mboumba, Denise P.
Baranek, Thomas
Wiesner, Jochen
Jomaa, Hassan
Kremsner, Peter G.
description Background. Fosmidomycin is a new antimalarial drug with a novel mechanism of action. Studies in Africa that have evaluated fosmidomycin as monotherapeutic agent demonstrated its excellent tolerance, but 3-timesdaily treatment regimens of ⩾4 days were required to achieve radical cure, prompting further research to identify and validate a suitable combination partner to enhance its efficacy. Methods. We conducted a randomized, controlled, open-label study to evaluate the efficacy and safety of fosmidomycin combined with clindamycin (n = 12; 30 and 5mg/kg body weight every 12 h for 5 days, respectively), compared with fosmidomycin alone (n = 12; 30 mg/kg body weight every 12 h for 5 days) and clindamycin alone (n = 12; 5 mg/kg body weight every 12 h for 5 days) for the clearance of asymptomatic Plasmodium falciparum infections in schoolchildren in Gabon aged 7–14 years. Results. Asexual parasites were rapidly cleared in children treated with fosmidomycin-clindamycin (median time, 18 h) and fosmidomycin alone (25 h) but slowly in children treated with clindamycin alone (71 h; P = .004). However, only treatment with fosmidomycin-clindamycin or clindamycin alone led to the radical elimination of asexual parasites as measured by day 14 and 28 cure rates of 100%. Asexual parasites reappeared by day 28 in 7 children who received fosmidomycin (day 14 cure rate, 92% [11/12; day 28 cure rate, 42% [5/12]). All regimens were well tolerated, and no serious adverse events occurred. Conclusion. The combination of fosmidomycin and clindamycin is well tolerated and superior to either agent on its own with respect to the rapid and radical clearance of P. falciparum infections in African children.
doi_str_mv 10.1086/381785
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Fosmidomycin is a new antimalarial drug with a novel mechanism of action. Studies in Africa that have evaluated fosmidomycin as monotherapeutic agent demonstrated its excellent tolerance, but 3-timesdaily treatment regimens of ⩾4 days were required to achieve radical cure, prompting further research to identify and validate a suitable combination partner to enhance its efficacy. Methods. We conducted a randomized, controlled, open-label study to evaluate the efficacy and safety of fosmidomycin combined with clindamycin (n = 12; 30 and 5mg/kg body weight every 12 h for 5 days, respectively), compared with fosmidomycin alone (n = 12; 30 mg/kg body weight every 12 h for 5 days) and clindamycin alone (n = 12; 5 mg/kg body weight every 12 h for 5 days) for the clearance of asymptomatic Plasmodium falciparum infections in schoolchildren in Gabon aged 7–14 years. Results. Asexual parasites were rapidly cleared in children treated with fosmidomycin-clindamycin (median time, 18 h) and fosmidomycin alone (25 h) but slowly in children treated with clindamycin alone (71 h; P = .004). However, only treatment with fosmidomycin-clindamycin or clindamycin alone led to the radical elimination of asexual parasites as measured by day 14 and 28 cure rates of 100%. Asexual parasites reappeared by day 28 in 7 children who received fosmidomycin (day 14 cure rate, 92% [11/12; day 28 cure rate, 42% [5/12]). All regimens were well tolerated, and no serious adverse events occurred. Conclusion. 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Psychology ; Gabon ; Gametocytes ; Hemoglobins - drug effects ; Hemoglobins - metabolism ; Humans ; Infections ; Infectious diseases ; Malaria ; Malaria, Falciparum - drug therapy ; Medical cures ; Medical sciences ; Microbiology ; Parasitemia ; Parasites ; Plasmodium falciparum ; Research Design</subject><ispartof>The Journal of infectious diseases, 2004-03, Vol.189 (5), p.901-908</ispartof><rights>Copyright 2003 Infectious Diseases Society of America</rights><rights>2004 by the Infectious Diseases Society of America 2004</rights><rights>2004 INIST-CNRS</rights><rights>Copyright University of Chicago, acting through its Press Mar 1 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-87226b17fba57ee50578e286568953112bf37fce75a1f4bce8249367a486d90d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30075910$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30075910$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15764983$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14976608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borrmann, Steffen</creatorcontrib><creatorcontrib>Adegnika, Ayola A.</creatorcontrib><creatorcontrib>Matsiegui, Pierre-Blaise</creatorcontrib><creatorcontrib>Issifou, Saadou</creatorcontrib><creatorcontrib>Schindler, Andreas</creatorcontrib><creatorcontrib>Mawili-Mboumba, Denise P.</creatorcontrib><creatorcontrib>Baranek, Thomas</creatorcontrib><creatorcontrib>Wiesner, Jochen</creatorcontrib><creatorcontrib>Jomaa, Hassan</creatorcontrib><creatorcontrib>Kremsner, Peter G.</creatorcontrib><title>Fosmidomycin-Clindamycin for Plasmodium falciparum Infections in African Children</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><addtitle>J Infect Dis</addtitle><description>Background. Fosmidomycin is a new antimalarial drug with a novel mechanism of action. Studies in Africa that have evaluated fosmidomycin as monotherapeutic agent demonstrated its excellent tolerance, but 3-timesdaily treatment regimens of ⩾4 days were required to achieve radical cure, prompting further research to identify and validate a suitable combination partner to enhance its efficacy. Methods. We conducted a randomized, controlled, open-label study to evaluate the efficacy and safety of fosmidomycin combined with clindamycin (n = 12; 30 and 5mg/kg body weight every 12 h for 5 days, respectively), compared with fosmidomycin alone (n = 12; 30 mg/kg body weight every 12 h for 5 days) and clindamycin alone (n = 12; 5 mg/kg body weight every 12 h for 5 days) for the clearance of asymptomatic Plasmodium falciparum infections in schoolchildren in Gabon aged 7–14 years. Results. Asexual parasites were rapidly cleared in children treated with fosmidomycin-clindamycin (median time, 18 h) and fosmidomycin alone (25 h) but slowly in children treated with clindamycin alone (71 h; P = .004). However, only treatment with fosmidomycin-clindamycin or clindamycin alone led to the radical elimination of asexual parasites as measured by day 14 and 28 cure rates of 100%. Asexual parasites reappeared by day 28 in 7 children who received fosmidomycin (day 14 cure rate, 92% [11/12; day 28 cure rate, 42% [5/12]). All regimens were well tolerated, and no serious adverse events occurred. Conclusion. The combination of fosmidomycin and clindamycin is well tolerated and superior to either agent on its own with respect to the rapid and radical clearance of P. falciparum infections in African children.</description><subject>Antimalarials</subject><subject>Antimalarials - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Blood</subject><subject>Body weight</subject><subject>Child</subject><subject>Clindamycin - adverse effects</subject><subject>Clindamycin - therapeutic use</subject><subject>Cohort Studies</subject><subject>Dosage</subject><subject>Drug Therapy, Combination</subject><subject>Fosfomycin - adverse effects</subject><subject>Fosfomycin - analogs &amp; derivatives</subject><subject>Fosfomycin - therapeutic use</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Gabon</topic><topic>Gametocytes</topic><topic>Hemoglobins - drug effects</topic><topic>Hemoglobins - metabolism</topic><topic>Humans</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Malaria</topic><topic>Malaria, Falciparum - drug therapy</topic><topic>Medical cures</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Parasitemia</topic><topic>Parasites</topic><topic>Plasmodium falciparum</topic><topic>Research Design</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borrmann, Steffen</creatorcontrib><creatorcontrib>Adegnika, Ayola A.</creatorcontrib><creatorcontrib>Matsiegui, Pierre-Blaise</creatorcontrib><creatorcontrib>Issifou, Saadou</creatorcontrib><creatorcontrib>Schindler, Andreas</creatorcontrib><creatorcontrib>Mawili-Mboumba, Denise P.</creatorcontrib><creatorcontrib>Baranek, Thomas</creatorcontrib><creatorcontrib>Wiesner, Jochen</creatorcontrib><creatorcontrib>Jomaa, Hassan</creatorcontrib><creatorcontrib>Kremsner, Peter G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borrmann, Steffen</au><au>Adegnika, Ayola A.</au><au>Matsiegui, Pierre-Blaise</au><au>Issifou, Saadou</au><au>Schindler, Andreas</au><au>Mawili-Mboumba, Denise P.</au><au>Baranek, Thomas</au><au>Wiesner, Jochen</au><au>Jomaa, Hassan</au><au>Kremsner, Peter G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fosmidomycin-Clindamycin for Plasmodium falciparum Infections in African Children</atitle><jtitle>The Journal of infectious diseases</jtitle><stitle>J Infect Dis</stitle><addtitle>J Infect Dis</addtitle><date>2004-03-01</date><risdate>2004</risdate><volume>189</volume><issue>5</issue><spage>901</spage><epage>908</epage><pages>901-908</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><coden>JIDIAQ</coden><abstract>Background. Fosmidomycin is a new antimalarial drug with a novel mechanism of action. Studies in Africa that have evaluated fosmidomycin as monotherapeutic agent demonstrated its excellent tolerance, but 3-timesdaily treatment regimens of ⩾4 days were required to achieve radical cure, prompting further research to identify and validate a suitable combination partner to enhance its efficacy. Methods. We conducted a randomized, controlled, open-label study to evaluate the efficacy and safety of fosmidomycin combined with clindamycin (n = 12; 30 and 5mg/kg body weight every 12 h for 5 days, respectively), compared with fosmidomycin alone (n = 12; 30 mg/kg body weight every 12 h for 5 days) and clindamycin alone (n = 12; 5 mg/kg body weight every 12 h for 5 days) for the clearance of asymptomatic Plasmodium falciparum infections in schoolchildren in Gabon aged 7–14 years. Results. Asexual parasites were rapidly cleared in children treated with fosmidomycin-clindamycin (median time, 18 h) and fosmidomycin alone (25 h) but slowly in children treated with clindamycin alone (71 h; P = .004). However, only treatment with fosmidomycin-clindamycin or clindamycin alone led to the radical elimination of asexual parasites as measured by day 14 and 28 cure rates of 100%. Asexual parasites reappeared by day 28 in 7 children who received fosmidomycin (day 14 cure rate, 92% [11/12; day 28 cure rate, 42% [5/12]). All regimens were well tolerated, and no serious adverse events occurred. Conclusion. The combination of fosmidomycin and clindamycin is well tolerated and superior to either agent on its own with respect to the rapid and radical clearance of P. falciparum infections in African children.</abstract><cop>Chicago, IL</cop><pub>The University of Chicago Press</pub><pmid>14976608</pmid><doi>10.1086/381785</doi><tpages>8</tpages></addata></record>
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source Jstor Complete Legacy; Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection
subjects Antimalarials
Antimalarials - therapeutic use
Biological and medical sciences
Blood
Body weight
Child
Clindamycin - adverse effects
Clindamycin - therapeutic use
Cohort Studies
Dosage
Drug Therapy, Combination
Fosfomycin - adverse effects
Fosfomycin - analogs & derivatives
Fosfomycin - therapeutic use
Fundamental and applied biological sciences. Psychology
Gabon
Gametocytes
Hemoglobins - drug effects
Hemoglobins - metabolism
Humans
Infections
Infectious diseases
Malaria
Malaria, Falciparum - drug therapy
Medical cures
Medical sciences
Microbiology
Parasitemia
Parasites
Plasmodium falciparum
Research Design
title Fosmidomycin-Clindamycin for Plasmodium falciparum Infections in African Children
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