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Single-Dose Tafenoquine to Prevent Relapse ofPlasmodium vivaxMalaria

Authors :
Kalehiwot M Wubie
Marcus V. G. Lacerda
Françoise Brand
Kim Fletcher
Alemseged Abdissa
Nillawan Buathong
Elizabeth Hardaker
Harald Noedl
Victoria M Rousell
Ermias Diro
Jörg-Peter Kleim
Monica R. F. Costa
Brian Angus
John J Breton
Alejandro Llanos-Cuentas
Lynda Kellam
Reginaldo Z Mia
Marcelo A M Brito
Martin Casapia
Hans-Peter Beck
Fe Espino
Raul Chuquiyauri
Wuelton Marcelo Monteiro
Rezika Mohammed
Donna D Clover
Fernando Val
Sisay Getie
Justin A. Green
Dhelio Batista Pereira
Daniel Yilma
Stephan Duparc
Mauro Shugiro Tada
Cherinet Abebe
Ahmed Zeynudin
Siôn W. Jones
Khadeeja Mohamed
David L. Saunders
Cletus O Ugwuegbulam
Gavin C. K. W. Koh
Chanthap Lon
Srivicha Krudsood
Source :
The New England Journal of Medicine
Publication Year :
2019
Publisher :
Massachusetts Medical Society, 2019.

Abstract

Background Treatment of Plasmodium vivax malaria requires the clearing of asexual parasites, but relapse can be prevented only if dormant hypnozoites are cleared from the liver (a treatment termed “radical cure”). Tafenoquine is a single-dose 8-aminoquinoline that has recently been registered for the radical cure of P. vivax. Methods This multicenter, double-blind, double-dummy, parallel group, randomized, placebo-controlled trial was conducted in Ethiopia, Peru, Brazil, Cambodia, Thailand, and the Philippines. We enrolled 522 patients with microscopically confirmed P. vivax infection (>100 to Results In the intention-to-treat population, the percentage of patients who were free from recurrence at 6 months was 62.4% in the tafenoquine group (95% confidence interval [CI], 54.9 to 69.0), 27.7% in the placebo group (95% CI, 19.6 to 36.6), and 69.6% in the primaquine group (95% CI, 60.2 to 77.1). The hazard ratio for the risk of recurrence was 0.30 (95% CI, 0.22 to 0.40) with tafenoquine as compared with placebo (P Conclusions Single-dose tafenoquine resulted in a significantly lower risk of P. vivax recurrence than placebo in patients with phenotypically normal G6PD activity. (Funded by GlaxoSmithKline and Medicines for Malaria Venture; DETECTIVE ClinicalTrials.gov number, NCT01376167. opens in new tab.)

Subjects

Subjects :
Male
double blind procedure
drug safety
Primaquine
Kaplan Meier method
Tafenoquine
Philippines
Plasmodium vivax
Kaplan-Meier Estimate
tafenoquine
Parasitemia
aminoquinoline derivative
030204 cardiovascular system & hematology
chloroquine
Hemoglobins
chemistry.chemical_compound
0302 clinical medicine
Chloroquine
Peru
Secondary Prevention
030212 general & internal medicine
Antimalarial Agent
disease free survival
methemoglobin
relapse
glucose 6 phosphate dehydrogenase
parasite clearance
biology
adult
Plasmodium vivax malaria
single drug dose
food and beverages
clinical trial
General Medicine
Thailand
enzyme activity
Intention to Treat Analysis
G6PD protein, human
female
Cytochrome P-450 CYP2D6
priority journal
retinal hypopigmentation
Aminoquinolines
disease severity
Drug Therapy, Combination
Cambodia
hypopigmentation
Brazil
recurrence risk
medicine.drug
combination drug therapy
Adolescent
hematocrit
Glucosephosphate Dehydrogenase
Disease-Free Survival
Article
Antimalarials
03 medical and health sciences
Pharmacotherapy
Double-Blind Method
retina disease
parasitic diseases
Malaria, Vivax
medicine
Humans
controlled study
human
procedures
cytochrome P450 2D6
dizziness
keratopathy
treatment duration
phase 3 clinical trial
antimalarial agent
isolation and purification
business.industry
statistical model
fungi
hemoglobin
medicine.disease
biology.organism_classification
major clinical study
Virology
purl.org/pe-repo/ocde/ford#3.02.00 [https]
phase 2 clinical trial
Logistic Models
multicenter study
chemistry
randomized controlled trial
placebo
Ethiopia
business
metabolism
Malaria

Details

ISSN :
15334406 and 00284793
Volume :
380
Database :
OpenAIRE
Journal :
New England Journal of Medicine
Accession number :
edsair.doi.dedup.....2d64bc83a97e78715cfe8f83b368a046
Full Text :
https://doi.org/10.1056/nejmoa1710775