Evidence map›Paper›PMID 25824212›Full record

Trial reportAntimicrobial agents and chemotherapy2015

Population pharmacokinetics of benznidazole in adult patients with Chagas disease.

D Soy, E Aldasoro, L Guerrero, E Posada, N Serret, T Mejía, J A Urbina, J Gascón

2 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 34 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 4 pooled it
5.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01755403 phase4completednot on this map

Population Pharmacokinetics in Benznidazole-treated Adults With Chronic Chagas Disease. Benznidazole Pharmacokinetics and Adverse Reactions Relationship.

TypeinterventionalSponsorBarcelona Centre for International Health ResearchRan2012 to 2013Enrolled52ConditionsChagas DiseaseArmsBenznidazole
NCT03981523 phase2completednot on this mapstarted 2019, after this paper: background citation

New Chemotherapy Regimens and Biomarkers for Chagas Disease

TypeinterventionalSponsorUniversity of Texas, El PasoRan2019 to 2024Enrolled450ConditionsTrypanosoma Cruzi Infection, Chagas DiseaseArmsBenznidazole, Nifurtimox
3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 4 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Ideal benznidazole dose regimen in chronic chagasic patients: a systematic review.Revista do Instituto de Medicina Tropical de Sao Paulo · 2020
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  12. Nanomedicines against Chagas disease: a critical review.Beilstein journal of nanotechnology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

D SoyPharmacy Service, Hospital Clinic Barcelona, Barcelona, Spain Institut de Investigació Biomèdica Agustí Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain CIBERES (CIBER de Enfermedades Respiratorias, 06/06/0028), Spain dsoy@clinic.ub.es.
E AldasoroInternational Health Service, Hospital Clinic Barcelona, Barcelona, Spain ISGlobal, Barcelona Center for International Health Research (CRESIB), Barcelona, Spain.
L GuerreroCIBERES (CIBER de Enfermedades Respiratorias, 06/06/0028), Spain CELLEX Laboratory, University of Barcelona, Barcelona, Spain.
E PosadaInternational Health Service, Hospital Clinic Barcelona, Barcelona, Spain ISGlobal, Barcelona Center for International Health Research (CRESIB), Barcelona, Spain.
N SerretInternational Health Service, Hospital Clinic Barcelona, Barcelona, Spain ISGlobal, Barcelona Center for International Health Research (CRESIB), Barcelona, Spain.
T MejíaInternational Health Service, Hospital Clinic Barcelona, Barcelona, Spain ISGlobal, Barcelona Center for International Health Research (CRESIB), Barcelona, Spain.
J A UrbinaInstituto Venezolano de Investigaciones Científicas, Caracas, Venezuela.
J GascónInternational Health Service, Hospital Clinic Barcelona, Barcelona, Spain ISGlobal, Barcelona Center for International Health Research (CRESIB), Barcelona, Spain.
Barcelona Institute for Global Health · ESHospital Clínic de Barcelona · ESUniversitat de Barcelona · ESInstituto Venezolano de Investigaciones Científicas · VE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of the present study was to build a population pharmacokinetic (popPK) model to characterize benznidazole (BNZ) pharmacokinetics in adults with chronic Chagas disease. This study was a prospective, open-label, single-center clinical trial approved by the local ethics committee. Patients received BNZ at 2.5 mg/kg of body weight/12 h (Abarax, Elea Laboratory, Argentina) for 60 days. Plasma BNZ samples were taken several times during the study and analyzed by high-performance liquid chromatography with UV-visible detection (HPLC-UV). The popPK analysis was done with NONMEMv.7.3. Demographic and biological data were tested as covariates. Intraindividual, interoccasion, and residual variabilities were modeled. Internal and external validations were completed to assess the robustness of the model. Later on, simulations were performed to generate BNZ concentration-time course profiles for different dosage regimens. A total of 358 plasma BNZ concentrations from 39 patients were included in the analysis. A one-compartment PK model characterized by clearance (CL/F) and the apparent volume of distribution (V/F), with first-order absorption (Ka) and elimination, adequately described the data (CL/F, 1.73 liters/h; V/F, 89.6 liters; and Ka, 1.15 h(-1)). No covariates were found to be significant for CL/F and V/F. Internal and external validations of the final model showed adequate results. Data from simulations revealed that a dose of 2.5 mg/kg/12 h might lead to overexposure in most patients. A lower dose (2.5 mg/kg/24 h) was able to achieve trough BNZ plasma concentrations within the accepted therapeutic range of 3 to 6 mg/liter. In summary, we developed a population PK model for BNZ in adults with chronic Chagas disease. Dosing simulations showed that a BNZ dose of 2.5 mg/kg/24 h will adequately keep BNZ trough plasma concentrations within the recommended target range for the majority of patients. (This study has been registered at EudraCT under number 2011-002900-34 and at ClinicalTrials.gov under number NCT01755403.).

Indexed as

AdultChagas DiseaseFemaleHumansMaleMiddle AgedNitroimidazolesTrypanocidal AgentsYoung AdultbenzonidazoleNitroimidazolesTrypanocidal Agents

Identifiers

PMID25824212
PMCPMC4432184
OpenAlexW2168925952

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.