Mostrar el registro sencillo del ítem

dc.contributor.author
Torrico, Faustino  
dc.contributor.author
Gascón, Joaquim  
dc.contributor.author
Ortiz, Lourdes  
dc.contributor.author
Pinto, Jimy  
dc.contributor.author
Rojas, Gimena  
dc.contributor.author
Palacios, Alejandro  
dc.contributor.author
Barreira, Fabiana  
dc.contributor.author
Blum, Bethania  
dc.contributor.author
Schijman, Alejandro Gabriel  
dc.contributor.author
Vaillant, Michel  
dc.contributor.author
Strub Wourgaft, Nathalie  
dc.contributor.author
Pinazo, Maria Jesus  
dc.contributor.author
Graeme, Bilbe  
dc.contributor.author
Ribeiro, Isabela  
dc.date.available
2023-09-18T09:58:11Z  
dc.date.issued
2023-02-01  
dc.identifier.citation
Torrico, Faustino; Gascón, Joaquim; Ortiz, Lourdes; Pinto, Jimy; Rojas, Gimena; et al.; A Phase 2, Randomized, Multicenter, Placebo-Controlled, Proof-of-Concept Trial of Oral Fexinidazole in Adults with Chronic Indeterminate Chagas Disease; Oxford University Press; Clinical Infectious Diseases; 76; 3; 1-2-2023; E1186-E1194  
dc.identifier.issn
1058-4838  
dc.identifier.uri
http://hdl.handle.net/11336/211744  
dc.description.abstract
Background: Chagas disease (CD) has significant global health impact, but safe, effective treatments remain elusive. The nitroimidazole fexinidazole is a potential treatment. Methods: This double-blind, randomized, placebo-controlled, dose-finding, proof-of-concept study was conducted in Bolivia. Adults with serologically confirmed chronic indeterminate CD and positive PCR were randomly assigned to 1 of 6 fexinidazole regimens (1200 or 1800 mg/day for 2, 4, or 8 weeks) or placebo. Target recruitment was 20 patients/arm. The primary endpoint was sustained parasitological clearance by serial negative qPCR from end of treatment (EOT) until 6 months follow-up in the intention-To-Treat (ITT) population. Follow-up was extended to 12 months. Results: Enrollment was interrupted after 4/47 patients presented with transient asymptomatic grade 3 and 4 neutropenia. Treatment of ongoing patients was stopped in all patients administered >2 weeks. A total of 40 patients received treatment with fexinidazole from 3 days to 8 weeks. Delayed-onset neutropenia (n = 8) and increased liver enzymes (n = 8) were found in fexinidazole patients vs none in the placebo arm. In the ITT analysis, sustained parasitological clearance from EOT to 12 months follow-up varied between 66.7% (1200 mg-2 week) and 100.0% (1800 mg-2 week). Rapid, sustained clearance of parasitemia was observed in all treated patients with available data, but not in any patients in the placebo group, at 12 months (P =. 0056). Further exploratory exposure-response analysis suggested low dosages of fexinidazole may be safe and effective. Conclusions: Further evaluation is needed to establish fexinidazole's minimum effective dosage and risk-benefit relationship. Results suggest potential for effective treatment regimens <10 days.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Oxford University Press  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
CHAGAS DISEASE  
dc.subject
FEXINIDAZOLE  
dc.subject
NEGLECTED TROPICAL DISEASES  
dc.subject
TRYPANOSOMA CRUZI  
dc.subject.classification
Enfermedades Infecciosas  
dc.subject.classification
Ciencias de la Salud  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
A Phase 2, Randomized, Multicenter, Placebo-Controlled, Proof-of-Concept Trial of Oral Fexinidazole in Adults with Chronic Indeterminate Chagas Disease  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2023-09-15T12:45:56Z  
dc.identifier.eissn
1537-6591  
dc.journal.volume
76  
dc.journal.number
3  
dc.journal.pagination
E1186-E1194  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Chicago  
dc.description.fil
Fil: Torrico, Faustino. Universidad Mayor de San Simón; Bolivia  
dc.description.fil
Fil: Gascón, Joaquim. Instituto de Salud Global de Barcelona; España  
dc.description.fil
Fil: Ortiz, Lourdes. Universidad Juan Misael Saracho de Tarija; Bolivia  
dc.description.fil
Fil: Pinto, Jimy. Universidad Mayor de San Simón; Bolivia  
dc.description.fil
Fil: Rojas, Gimena. Universidad Mayor de San Simón; Bolivia  
dc.description.fil
Fil: Palacios, Alejandro. Universidad Juan Misael Saracho de Tarija; Bolivia  
dc.description.fil
Fil: Barreira, Fabiana. Drugs For Neglected Diseases Initiative; Suiza  
dc.description.fil
Fil: Blum, Bethania. Drugs For Neglected Diseases Initiative; Suiza  
dc.description.fil
Fil: Schijman, Alejandro Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina  
dc.description.fil
Fil: Vaillant, Michel. Centre National de la Recherche Scientifique; Francia  
dc.description.fil
Fil: Strub Wourgaft, Nathalie. Drugs For Neglected Diseases Initiative; Suiza  
dc.description.fil
Fil: Pinazo, Maria Jesus. Drugs For Neglected Diseases Initiative; Suiza  
dc.description.fil
Fil: Graeme, Bilbe. Drugs For Neglected Diseases Initiative; Suiza  
dc.description.fil
Fil: Ribeiro, Isabela. Drugs For Neglected Diseases Initiative; Suiza  
dc.journal.title
Clinical Infectious Diseases  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/cid/article/76/3/e1186/6655743  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1093/cid/ciac579