Efficacy and Safety of a Single Dose of Ivermectin, Diethylcarbamazine, and Albendazole for Treatment of Lymphatic Filariasis in Côte d’Ivoire: An Open-label Randomized Controlled Trial
Abstract Background Improved drug regimens are needed to accelerate elimination of lymphatic filariasis in Africa. This study determined whether a single co-administered dose of ivermectin plus diethylcarbamazine plus albendazole [IDA] is noninferior to standard 3 annual doses of ivermectin plus alb...
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description | Abstract
Background
Improved drug regimens are needed to accelerate elimination of lymphatic filariasis in Africa. This study determined whether a single co-administered dose of ivermectin plus diethylcarbamazine plus albendazole [IDA] is noninferior to standard 3 annual doses of ivermectin plus albendazole (IA) used in many LF-endemic areas of Africa.
Methods
Treatment-naive adults with Wuchereria bancrofti microfilaremia in Côte d’Ivoire were randomized to receive a single dose of IDA (n = 43) or 3 annual doses of IA (n = 52) in an open-label, single-blinded trial. The primary endpoint was the proportion of participants who were microfilaria (Mf) negative at 36 months. Secondary endpoints were Mf clearance at 6, 12, and 24 months; inactivation of adult worm nests; and safety.
Results
At 36 months posttreatment with IDA, 18/33 (55%; 95% CI, 38–72%) cleared Mf versus 33/42 (79%; 67–91%) with IA (P = .045). At 6 and 12 months IDA was superior to IA in clearing Mf (89% [77–99%] and 71% [56–85%]), respectively, versus 34% (20–48%) and 26% (14–42%) (P < .001). IDA was equivalent to IA at 24 months (61% [45–77%] vs 54% [38–72%]; P = .53). IDA was superior to IA for inactivating adult worms at all time points. Both treatments were well tolerated, and there were no serious adverse events.
Conclusions
A single dose of IDA was superior to 2 doses of IA in reducing the overall Mf burden by 24 months. Reinfection may have contributed to the lack of sustained clearance of Mf with IDA.
Clinical Trials Registration
NCT02974049.
A single dose of ivermectin, diethylcarbamazine, and albendazole is superior to standard treatment with ivermectin and albendazole for microfilarial clearance at 6 and 12 months and equivalent to 2 annual doses of ivermectin and albendazole at 24 months. |
doi_str_mv | 10.1093/cid/ciz1050 |
format | Article |
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Background
Improved drug regimens are needed to accelerate elimination of lymphatic filariasis in Africa. This study determined whether a single co-administered dose of ivermectin plus diethylcarbamazine plus albendazole [IDA] is noninferior to standard 3 annual doses of ivermectin plus albendazole (IA) used in many LF-endemic areas of Africa.
Methods
Treatment-naive adults with Wuchereria bancrofti microfilaremia in Côte d’Ivoire were randomized to receive a single dose of IDA (n = 43) or 3 annual doses of IA (n = 52) in an open-label, single-blinded trial. The primary endpoint was the proportion of participants who were microfilaria (Mf) negative at 36 months. Secondary endpoints were Mf clearance at 6, 12, and 24 months; inactivation of adult worm nests; and safety.
Results
At 36 months posttreatment with IDA, 18/33 (55%; 95% CI, 38–72%) cleared Mf versus 33/42 (79%; 67–91%) with IA (P = .045). At 6 and 12 months IDA was superior to IA in clearing Mf (89% [77–99%] and 71% [56–85%]), respectively, versus 34% (20–48%) and 26% (14–42%) (P < .001). IDA was equivalent to IA at 24 months (61% [45–77%] vs 54% [38–72%]; P = .53). IDA was superior to IA for inactivating adult worms at all time points. Both treatments were well tolerated, and there were no serious adverse events.
Conclusions
A single dose of IDA was superior to 2 doses of IA in reducing the overall Mf burden by 24 months. Reinfection may have contributed to the lack of sustained clearance of Mf with IDA.
Clinical Trials Registration
NCT02974049.
A single dose of ivermectin, diethylcarbamazine, and albendazole is superior to standard treatment with ivermectin and albendazole for microfilarial clearance at 6 and 12 months and equivalent to 2 annual doses of ivermectin and albendazole at 24 months.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciz1050</identifier><identifier>PMID: 31641754</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Albendazole - adverse effects ; Animals ; Cote d'Ivoire - epidemiology ; Diethylcarbamazine - adverse effects ; Drug Therapy, Combination ; Elephantiasis, Filarial - drug therapy ; Filaricides - adverse effects ; Ivermectin - adverse effects ; Online Only ; Wuchereria bancrofti</subject><ispartof>Clinical infectious diseases, 2020-10, Vol.71 (7), p.e68-e75</ispartof><rights>The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. 2019</rights><rights>The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-381ecc0bc167d5446adf5266ef54a7ea51fa5f39490472da466b4a15f7332fd13</citedby><cites>FETCH-LOGICAL-c412t-381ecc0bc167d5446adf5266ef54a7ea51fa5f39490472da466b4a15f7332fd13</cites><orcidid>0000-0003-3873-7860</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31641754$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bjerum, Catherine M</creatorcontrib><creatorcontrib>Ouattara, Allassane F</creatorcontrib><creatorcontrib>Aboulaye, Méité</creatorcontrib><creatorcontrib>Kouadio, Olivier</creatorcontrib><creatorcontrib>Marius, Vanga K</creatorcontrib><creatorcontrib>Andersen, Britt J</creatorcontrib><creatorcontrib>Weil, Gary J</creatorcontrib><creatorcontrib>Koudou, Benjamin G</creatorcontrib><creatorcontrib>King, Christopher L</creatorcontrib><title>Efficacy and Safety of a Single Dose of Ivermectin, Diethylcarbamazine, and Albendazole for Treatment of Lymphatic Filariasis in Côte d’Ivoire: An Open-label Randomized Controlled Trial</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Abstract
Background
Improved drug regimens are needed to accelerate elimination of lymphatic filariasis in Africa. This study determined whether a single co-administered dose of ivermectin plus diethylcarbamazine plus albendazole [IDA] is noninferior to standard 3 annual doses of ivermectin plus albendazole (IA) used in many LF-endemic areas of Africa.
Methods
Treatment-naive adults with Wuchereria bancrofti microfilaremia in Côte d’Ivoire were randomized to receive a single dose of IDA (n = 43) or 3 annual doses of IA (n = 52) in an open-label, single-blinded trial. The primary endpoint was the proportion of participants who were microfilaria (Mf) negative at 36 months. Secondary endpoints were Mf clearance at 6, 12, and 24 months; inactivation of adult worm nests; and safety.
Results
At 36 months posttreatment with IDA, 18/33 (55%; 95% CI, 38–72%) cleared Mf versus 33/42 (79%; 67–91%) with IA (P = .045). At 6 and 12 months IDA was superior to IA in clearing Mf (89% [77–99%] and 71% [56–85%]), respectively, versus 34% (20–48%) and 26% (14–42%) (P < .001). IDA was equivalent to IA at 24 months (61% [45–77%] vs 54% [38–72%]; P = .53). IDA was superior to IA for inactivating adult worms at all time points. Both treatments were well tolerated, and there were no serious adverse events.
Conclusions
A single dose of IDA was superior to 2 doses of IA in reducing the overall Mf burden by 24 months. Reinfection may have contributed to the lack of sustained clearance of Mf with IDA.
Clinical Trials Registration
NCT02974049.
A single dose of ivermectin, diethylcarbamazine, and albendazole is superior to standard treatment with ivermectin and albendazole for microfilarial clearance at 6 and 12 months and equivalent to 2 annual doses of ivermectin and albendazole at 24 months.</description><subject>Albendazole - adverse effects</subject><subject>Animals</subject><subject>Cote d'Ivoire - epidemiology</subject><subject>Diethylcarbamazine - adverse effects</subject><subject>Drug Therapy, Combination</subject><subject>Elephantiasis, Filarial - drug therapy</subject><subject>Filaricides - adverse effects</subject><subject>Ivermectin - adverse effects</subject><subject>Online Only</subject><subject>Wuchereria bancrofti</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kcFuEzEURS0EoiWwYo-8YkMH7NiembBAitIWIkWqRMN69MZ-bow8duSZRpqs-A3-gyU7_oQvwSGlgg0Ly0_2vceyDiHPOXvN2Uy80c7ktedMsQfklCtRFaWa8Yd5ZqouZC3qE_Kk7z8zxnnN1GNyIngpeaXkKfl-Ya3ToEcKwdBrsDiMNFoK9NqFG4_0PPZ4OFjuMHWoBxfO6LnDYTN6DamFDvYu4Nnv-ty3GAzsY-7ZmOg6IQwdhuEAWI3ddgOD0_TSeUgOetdTF-jix7cBqfn55etyF13Ct3Qe6NUWQ-GhRU8_ZnLs3B4NXcQwpOh9HtcZ4J-SRxZ8j8_u9gn5dHmxXnwoVlfvl4v5qtCST4dC1By1Zq3mZWWUlCUYq6ZliVZJqBAUt6CsmMkZk9XUgCzLVgJXthJiag0XE_LuyN3eth0anX-UwDfb5DpIYxPBNf_eBLdpbuKuqVQtZDYyIa-OAJ1i3ye0913OmoPEJkts7iTm9Iu_n7vP_rGWAy-PgXi7_S_pFyCVq48</recordid><startdate>20201023</startdate><enddate>20201023</enddate><creator>Bjerum, Catherine M</creator><creator>Ouattara, Allassane F</creator><creator>Aboulaye, Méité</creator><creator>Kouadio, Olivier</creator><creator>Marius, Vanga K</creator><creator>Andersen, Britt J</creator><creator>Weil, Gary J</creator><creator>Koudou, Benjamin G</creator><creator>King, Christopher L</creator><general>Oxford University Press</general><scope>TOX</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>5PM</scope><orcidid>https://orcid.org/0000-0003-3873-7860</orcidid></search><sort><creationdate>20201023</creationdate><title>Efficacy and Safety of a Single Dose of Ivermectin, Diethylcarbamazine, and Albendazole for Treatment of Lymphatic Filariasis in Côte d’Ivoire: An Open-label Randomized Controlled Trial</title><author>Bjerum, Catherine M ; Ouattara, Allassane F ; Aboulaye, Méité ; Kouadio, Olivier ; Marius, Vanga K ; Andersen, Britt J ; Weil, Gary J ; Koudou, Benjamin G ; King, Christopher L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-381ecc0bc167d5446adf5266ef54a7ea51fa5f39490472da466b4a15f7332fd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Albendazole - adverse effects</topic><topic>Animals</topic><topic>Cote d'Ivoire - epidemiology</topic><topic>Diethylcarbamazine - adverse effects</topic><topic>Drug Therapy, Combination</topic><topic>Elephantiasis, Filarial - drug therapy</topic><topic>Filaricides - adverse effects</topic><topic>Ivermectin - adverse effects</topic><topic>Online Only</topic><topic>Wuchereria bancrofti</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bjerum, Catherine M</creatorcontrib><creatorcontrib>Ouattara, Allassane F</creatorcontrib><creatorcontrib>Aboulaye, Méité</creatorcontrib><creatorcontrib>Kouadio, Olivier</creatorcontrib><creatorcontrib>Marius, Vanga K</creatorcontrib><creatorcontrib>Andersen, Britt J</creatorcontrib><creatorcontrib>Weil, Gary J</creatorcontrib><creatorcontrib>Koudou, Benjamin G</creatorcontrib><creatorcontrib>King, Christopher L</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bjerum, Catherine M</au><au>Ouattara, Allassane F</au><au>Aboulaye, Méité</au><au>Kouadio, Olivier</au><au>Marius, Vanga K</au><au>Andersen, Britt J</au><au>Weil, Gary J</au><au>Koudou, Benjamin G</au><au>King, Christopher L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy and Safety of a Single Dose of Ivermectin, Diethylcarbamazine, and Albendazole for Treatment of Lymphatic Filariasis in Côte d’Ivoire: An Open-label Randomized Controlled Trial</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2020-10-23</date><risdate>2020</risdate><volume>71</volume><issue>7</issue><spage>e68</spage><epage>e75</epage><pages>e68-e75</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Abstract
Background
Improved drug regimens are needed to accelerate elimination of lymphatic filariasis in Africa. This study determined whether a single co-administered dose of ivermectin plus diethylcarbamazine plus albendazole [IDA] is noninferior to standard 3 annual doses of ivermectin plus albendazole (IA) used in many LF-endemic areas of Africa.
Methods
Treatment-naive adults with Wuchereria bancrofti microfilaremia in Côte d’Ivoire were randomized to receive a single dose of IDA (n = 43) or 3 annual doses of IA (n = 52) in an open-label, single-blinded trial. The primary endpoint was the proportion of participants who were microfilaria (Mf) negative at 36 months. Secondary endpoints were Mf clearance at 6, 12, and 24 months; inactivation of adult worm nests; and safety.
Results
At 36 months posttreatment with IDA, 18/33 (55%; 95% CI, 38–72%) cleared Mf versus 33/42 (79%; 67–91%) with IA (P = .045). At 6 and 12 months IDA was superior to IA in clearing Mf (89% [77–99%] and 71% [56–85%]), respectively, versus 34% (20–48%) and 26% (14–42%) (P < .001). IDA was equivalent to IA at 24 months (61% [45–77%] vs 54% [38–72%]; P = .53). IDA was superior to IA for inactivating adult worms at all time points. Both treatments were well tolerated, and there were no serious adverse events.
Conclusions
A single dose of IDA was superior to 2 doses of IA in reducing the overall Mf burden by 24 months. Reinfection may have contributed to the lack of sustained clearance of Mf with IDA.
Clinical Trials Registration
NCT02974049.
A single dose of ivermectin, diethylcarbamazine, and albendazole is superior to standard treatment with ivermectin and albendazole for microfilarial clearance at 6 and 12 months and equivalent to 2 annual doses of ivermectin and albendazole at 24 months.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>31641754</pmid><doi>10.1093/cid/ciz1050</doi><orcidid>https://orcid.org/0000-0003-3873-7860</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | Albendazole - adverse effects Animals Cote d'Ivoire - epidemiology Diethylcarbamazine - adverse effects Drug Therapy, Combination Elephantiasis, Filarial - drug therapy Filaricides - adverse effects Ivermectin - adverse effects Online Only Wuchereria bancrofti |
title | Efficacy and Safety of a Single Dose of Ivermectin, Diethylcarbamazine, and Albendazole for Treatment of Lymphatic Filariasis in Côte d’Ivoire: An Open-label Randomized Controlled Trial |
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