Publication:
Arterolane, a new synthetic trioxolane for treatment of uncomplicated Plasmodium falciparum malaria: A phase II, multicenter, randomized, dose-finding clinical trial

dc.contributor.authorNeena Valechaen_US
dc.contributor.authorSornchai Looareesuwanen_US
dc.contributor.authorAndreas Martenssonen_US
dc.contributor.authorSalim Mohammed Abdullaen_US
dc.contributor.authorSrivicha Krudsooden_US
dc.contributor.authorNoppadon Tangpukdeeen_US
dc.contributor.authorSanjib Mohantyen_US
dc.contributor.authorSaroj K. Mishraen_US
dc.contributor.authorP. K. Tyagien_US
dc.contributor.authorS. K. Sharmaen_US
dc.contributor.authorJoerg Moehrleen_US
dc.contributor.authorAnirudh Gautamen_US
dc.contributor.authorArjun Royen_US
dc.contributor.authorJyoti K. Paliwalen_US
dc.contributor.authorMonica Kotharien_US
dc.contributor.authorNilanjan Sahaen_US
dc.contributor.authorAditya P. Dashen_US
dc.contributor.authorAnders Björkmanen_US
dc.contributor.otherNational Institute of Malaria Research Indiaen_US
dc.contributor.otherIspat General Hospitalen_US
dc.contributor.otherRanbaxy Research Laboratoryen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherKarolinska University Hospitalen_US
dc.contributor.otherZanzibar Malaria Research Unit of Karolinska Instituteen_US
dc.contributor.otherIfakara Health Instituteen_US
dc.contributor.otherMedicines for Malaria Ventureen_US
dc.date.accessioned2018-09-24T09:21:12Z
dc.date.available2018-09-24T09:21:12Z
dc.date.issued2010-09-15en_US
dc.description.abstractBackground: Drug-resistant Plasmodium falciparum malaria necessitates development of novel drugs for treatment. The present study assessed the efficacy and safety of 3 dose levels of arterolane (RBx 11160), a synthetic trioxolane, for treatment of acute uncomplicated falciparum malaria. Methods: In this randomized, double-blind, multicenter, parallel-group, dose-finding, phase II trial, 230 patients from 4 centers in Thailand, India, and Tanzania (mainland and Zanzibar) received either 50 mg (n=78), 100 mg (n=76), or 200 mg (n=76) of arterolane once daily for 7 days. Patients (aged 13-65 years) with asexual parasite density of 1000-100,000 parasites/μL were included and were followed up for 28 days. The median time to 90% parasite clearance (PC90) was evaluated. Results: The median PC90was longer in the group receiving the 50-mg dose (19.4 h), compared with the groups receiving the 100-mg dose (12.8 h) and 200-mg dose (12.6 h) (P < .01). The polymerase chain reaction- corrected adequate clinical and parasitological responses on day 28 were 63%, 71%, and 72% for the groups receiving the 50-mg, 100-mg, and 200-mg doses, respectively, by intention-to-treat analysis (odds ratio, 1.55; 95% confidence interval, 0.78-3.06, for comparison of the 200-mg and 50-mg dose groups). Treatment was generally well tolerated. No patient died or experienced any serious adverse event. Mild complaints were reported in <10% of the patients and were similar in the 3 groups. Biochemistry and hematological analyses did not show any sign of drug toxicity in any patient. Conclusion: Arterolane at daily doses of 100 and 200 mg is a rapidly acting, effective, and safe synthetic antimalarial drug, which may potentially represent an alternative to artemisinin derivatives in antimalarial combination therapy. © 2010 by the Infectious Diseases Society of America. All rights reserved.en_US
dc.identifier.citationClinical Infectious Diseases. Vol.51, No.6 (2010), 684-691en_US
dc.identifier.doi10.1086/655831en_US
dc.identifier.issn10584838en_US
dc.identifier.other2-s2.0-77955951674en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29532
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955951674&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleArterolane, a new synthetic trioxolane for treatment of uncomplicated Plasmodium falciparum malaria: A phase II, multicenter, randomized, dose-finding clinical trialen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77955951674&origin=inwarden_US

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