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 |
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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. 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><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1086/381785</identifier><identifier>PMID: 14976608</identifier><identifier>CODEN: JIDIAQ</identifier><language>eng</language><publisher>Chicago, IL: The University of Chicago Press</publisher><subject>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</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&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 & derivatives</subject><subject>Fosfomycin - therapeutic use</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gabon</subject><subject>Gametocytes</subject><subject>Hemoglobins - drug effects</subject><subject>Hemoglobins - metabolism</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Malaria</subject><subject>Malaria, Falciparum - drug therapy</subject><subject>Medical cures</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Parasitemia</subject><subject>Parasites</subject><subject>Plasmodium falciparum</subject><subject>Research Design</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10NGK1DAUBuAgijuu-gZKV9C7atI0Ocnl2nWdhQUVFcWbkKYJZmyTMWnBfXujHXZA8CoHzsefw4_QY4JfEiz4KyoICHYHbQijUHNO6F20wbhpaiKkPEEPct5hjFvK4T46Ia0EzrHYoA-XMU9-iNON8aHuRh8G_XeuXEzV-1HnKQ5-mSqnR-P3OpXxKjhrZh9Droo7d8kbHaruux-HZMNDdK_YbB8d3lP0-fLNp25bX797e9WdX9emZWSuBTQN7wm4XjOwlmEGwjaCMy4ko4Q0vaPgjAWmiWt7Y0XTynK9bgUfJB7oKXqx5u5T_LnYPKvJZ2PHUQcbl6wISC5bEAU--wfu4pJCuU01DZWYg4Rjmkkx52Sd2ic_6XSjCFZ_GlZrwwU-PaQt_WSHIztUWsDzA9DZ6NElHYzPR8eAt1LQ4s5WF5f9_z97sppdnmO6VRRjYJLgsq_Xvc-z_XW71-mH4kCBqe3Xb-riy0dgF9tOvaa_AXQ9o9E</recordid><startdate>20040301</startdate><enddate>20040301</enddate><creator>Borrmann, Steffen</creator><creator>Adegnika, Ayola A.</creator><creator>Matsiegui, Pierre-Blaise</creator><creator>Issifou, Saadou</creator><creator>Schindler, Andreas</creator><creator>Mawili-Mboumba, Denise P.</creator><creator>Baranek, Thomas</creator><creator>Wiesner, Jochen</creator><creator>Jomaa, Hassan</creator><creator>Kremsner, Peter G.</creator><general>The University of Chicago Press</general><general>University of Chicago Press</general><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>M7N</scope></search><sort><creationdate>20040301</creationdate><title>Fosmidomycin-Clindamycin for Plasmodium falciparum Infections in African Children</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-87226b17fba57ee50578e286568953112bf37fce75a1f4bce8249367a486d90d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Antimalarials</topic><topic>Antimalarials - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Blood</topic><topic>Body weight</topic><topic>Child</topic><topic>Clindamycin - adverse effects</topic><topic>Clindamycin - therapeutic use</topic><topic>Cohort Studies</topic><topic>Dosage</topic><topic>Drug Therapy, Combination</topic><topic>Fosfomycin - adverse effects</topic><topic>Fosfomycin - analogs & derivatives</topic><topic>Fosfomycin - therapeutic use</topic><topic>Fundamental and applied biological sciences. 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 & Medical Complete (Alumni)</collection><collection>Nursing & 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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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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