TY - JOUR
T1 - New regimens of benznidazole for the treatment of chronic Chagas disease in adult participants in indeterminate form or with mild cardiac progression (NuestroBen study)
T2 - protocol for a phase III randomised, multicentre non-inferiority clinical trial
AU - Marques, Tayná
AU - Forsyth, Colin
AU - Barreira, Fabiana
AU - Lombas, Carola
AU - Blum de Oliveira, Bethania
AU - Laserna, Mónica
AU - Molina, Israel
AU - Bangher, Maria Del Carmen
AU - Javier Fernández, Rosmiro
AU - Lloveras, Susana
AU - Fernández, Marisa Liliana
AU - Scapellato, Pablo
AU - Patterson, Patricia
AU - Garcia, Wilson
AU - Ortiz, Lourdes
AU - Schijman, Alejandro
AU - Moreira, Otacilio C
AU - García, Lineth
AU - Viele, Kert
AU - Longhi, Silvia
AU - Vaillant, Michel
AU - Tipple, Craig
AU - Fraisse, Laurent
AU - Silvestre-Sousa, Andrea
AU - Sosa-Estani, Sergio
AU - Pinazo, María-Jesús
N1 - Funding:
The study is supported by the Drugs for Neglected Diseases initiative
(DNDi), ELEA-Phoenix S.A., and Fundación Mundo Sano-Argentina. The DNDi is
grateful to its donors, public and private, who have provided funding to DNDi since
its inception in 2003. A full list of DNDi’s donors can be found at http://www.dndi.
org/about/donors/
© Author(s) (or their employer(s)) 2025. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group.
PY - 2025/9/30
Y1 - 2025/9/30
N2 - INTRODUCTION: Chagas disease (CD) is one of the most neglected diseases in the world. In Latin America, CD is endemic in 21 countries, with an estimated 70 million people at risk of infection. Current treatments are limited to two nitroheterocyclic compounds: nifurtimox and benznidazole (BZN). Each has significant limitations, including long duration and safety concerns. However, data from recently completed studies suggest that reduced-duration regimens may be equally effective while enhancing safety.METHODS AND ANALYSIS: NuestroBen is a phase III, randomised, multicentre clinical trial designed to assess whether shorter (2- and 4-week) regimens of BZN are non-inferior to the standard 8-week treatment. A total of 540 adult participants with no evidence of organ damage (the indeterminate form) or with mild cardiac progression (mild electrocardiographic alterations and without systolic dysfunction or symptoms), all in the chronic phase of CD, will be recruited at six study sites in Argentina and two study sites in Bolivia. Participants will be randomised to receive one of the two shortened regimens of BZN (300 mg per day for 2 or 4 weeks) or standard treatment (300 mg per day for 8 weeks). The primary endpoint is sustained elimination of parasitaemia from the end of treatment through 12 months of follow-up. Secondary endpoints will assess sustained clearance of parasitaemia at 1, 4, 6 and 8 months of follow-up from the end of treatment, drug tolerability and adherence to treatment. NuestroBen will also evaluate whether two shortened regimens of BZN improve drug tolerability and treatment adherence compared with the current standard treatment while maintaining efficacy in participants with the indeterminate form of CD or with mild cardiac involvement.ETHICS AND DISSEMINATION: In Argentina, this study was approved by
Fundación de Estudios Farmacológicos y Medicamentos 'Luis M. Zieher' for its conduct at the
Instituto de Cardiología de Corrientes 'Juana Francisca Cabral' (reference: NuestroBen-2020/2021) and the
Instituto Nacional de Parasitología 'Dr. Mario Fatala Chaben' (reference: NuestroBen-2020/2021) by
Comité Institucional de Ética de Investigación en Salud for the
Centro de Chagas y Patología Regional de Santiago del Estero (reference: NuestroBen-2020-088/2021), by
Comité de Ética en Investigación for the
Hospital de Infecciosas F.J. Muñiz (reference: NuestroBen-2020-4037) and the
Hospital General de Agudos D.F. Santojanni (reference: NuestroBen-2020-4039) and by
Comité de Bioética for the
Fundación Huésped (reference: NuestroBen-2020/2021). In Bolivia, it was approved by
Comité de Ética en Investigación en Salud from the
Universidad Autónoma Juan Misael Saracho (reference: NuestroBen-2020/2025). All participants are asked to provide written informed consent to participate. Recruitment processes started in July 2023, and as of 15 June 2025, 140 participants have been recruited. Findings will be shared with Argentinian and Bolivian public health officials and with the Chagas and tropical medicine communities via international conferences. Findings will also be published in medical journals.
TRIAL REGISTRATION NUMBER: NCT04897516.
AB - INTRODUCTION: Chagas disease (CD) is one of the most neglected diseases in the world. In Latin America, CD is endemic in 21 countries, with an estimated 70 million people at risk of infection. Current treatments are limited to two nitroheterocyclic compounds: nifurtimox and benznidazole (BZN). Each has significant limitations, including long duration and safety concerns. However, data from recently completed studies suggest that reduced-duration regimens may be equally effective while enhancing safety.METHODS AND ANALYSIS: NuestroBen is a phase III, randomised, multicentre clinical trial designed to assess whether shorter (2- and 4-week) regimens of BZN are non-inferior to the standard 8-week treatment. A total of 540 adult participants with no evidence of organ damage (the indeterminate form) or with mild cardiac progression (mild electrocardiographic alterations and without systolic dysfunction or symptoms), all in the chronic phase of CD, will be recruited at six study sites in Argentina and two study sites in Bolivia. Participants will be randomised to receive one of the two shortened regimens of BZN (300 mg per day for 2 or 4 weeks) or standard treatment (300 mg per day for 8 weeks). The primary endpoint is sustained elimination of parasitaemia from the end of treatment through 12 months of follow-up. Secondary endpoints will assess sustained clearance of parasitaemia at 1, 4, 6 and 8 months of follow-up from the end of treatment, drug tolerability and adherence to treatment. NuestroBen will also evaluate whether two shortened regimens of BZN improve drug tolerability and treatment adherence compared with the current standard treatment while maintaining efficacy in participants with the indeterminate form of CD or with mild cardiac involvement.ETHICS AND DISSEMINATION: In Argentina, this study was approved by
Fundación de Estudios Farmacológicos y Medicamentos 'Luis M. Zieher' for its conduct at the
Instituto de Cardiología de Corrientes 'Juana Francisca Cabral' (reference: NuestroBen-2020/2021) and the
Instituto Nacional de Parasitología 'Dr. Mario Fatala Chaben' (reference: NuestroBen-2020/2021) by
Comité Institucional de Ética de Investigación en Salud for the
Centro de Chagas y Patología Regional de Santiago del Estero (reference: NuestroBen-2020-088/2021), by
Comité de Ética en Investigación for the
Hospital de Infecciosas F.J. Muñiz (reference: NuestroBen-2020-4037) and the
Hospital General de Agudos D.F. Santojanni (reference: NuestroBen-2020-4039) and by
Comité de Bioética for the
Fundación Huésped (reference: NuestroBen-2020/2021). In Bolivia, it was approved by
Comité de Ética en Investigación en Salud from the
Universidad Autónoma Juan Misael Saracho (reference: NuestroBen-2020/2025). All participants are asked to provide written informed consent to participate. Recruitment processes started in July 2023, and as of 15 June 2025, 140 participants have been recruited. Findings will be shared with Argentinian and Bolivian public health officials and with the Chagas and tropical medicine communities via international conferences. Findings will also be published in medical journals.
TRIAL REGISTRATION NUMBER: NCT04897516.
KW - Humans
KW - Nitroimidazoles/administration & dosage
KW - Trypanocidal Agents/administration & dosage
KW - Chagas Disease/drug therapy
KW - Adult
KW - Chronic Disease
KW - Argentina
KW - Clinical Trials, Phase III as Topic
KW - Female
KW - Disease Progression
KW - Male
KW - Randomized Controlled Trials as Topic
KW - Multicenter Studies as Topic
KW - Bolivia
KW - Equivalence Trials as Topic
KW - Treatment Outcome
KW - Middle Aged
UR - https://pubmed.ncbi.nlm.nih.gov/41027700/
U2 - 10.1136/bmjopen-2024-098079
DO - 10.1136/bmjopen-2024-098079
M3 - Article
C2 - 41027700
SN - 2044-6055
VL - 15
JO - BMJ Open
JF - BMJ Open
IS - 9
M1 - e098079
ER -