Population Pharmacokinetics Study of Benznidazole in Children With Chagas'Disease

Chagas' Disease Clinical Trial

— Pop PK Chagas  

Official title:

Population Pharmacokinetics Study of Benznidazole in Children With Chagas'Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01549236
• Other study ID #: DNDi-CD-PEDBZ-001
• Status: Completed
• Phase: Phase 4
• Start date: May 2011
• Est. completion date: October 2012

Study information

• Verified date: August 2012
• Source: Drugs for Neglected Diseases
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to describe the population pharmacokinetics parameters of benznidazole in children with acute or early chronic indeterminate form of Chagas Disease.

Description:

Treatment of Chagas disease (CD) has been always focused on pediatric population. Initially, treatment was recommended only to acute and congenital cases (including newborns diagnosed at birth), with good parasitological response of 60% to 85% of patients in the acute phase and more than 90% of congenitally infected infants treated in the first year of life.

Despite existing treatment recommendations for children with CD (from birth to 12y), there is no formulation available that meets the needs of target pediatric population, especially the younger age groups. Benznidazole (Bz), developed over 30 years ago and the main drug of choice, is only available in an 'adult' tablet strength of 100 mg (LAFEPE Benznidazol®).

With the lack of pediatric formulation, the 100mg tablet needs to be fractionated in ½ and ¼ tablets or prepared as extemporaneous formulations (macerated, diluted, suspension, etc) to adjust the dose to patient weight, often leading to sub or over-dosing, which may affect safety and efficacy of the treatment. With regards to children, there is an absolute lack of information on Bz PK in the pediatric population and its relationship with treatment safety and efficacy.

In order to respond to the need of a age-adapted, easy to use pediatric formulation, DNDi and LAFEPE have joined efforts to develop a 12.5 mg dispersible Bz tablet targeting treatment of CD in children < 20 Kg. Once this formulation is available, two pharmacokinetics studies are planned to be conducted: a comparative bioavailability study in adult healthy normal volunteers and a population pharmacokinetics study in young children.

The group of newborns, from birth to - 2 years-old children, has been included as they represent the population of congenital cases. Current estimates of positive serology for CD in women at reproductive age vary considerably from country-to-country ranging from 5-40%, with vertical transmission rates of up to 12%. There is consensus that congenital infection may remain an important mode of transmission for another generation, and appropriate treatment targeting newborns is a possible control strategy (with very high chances of cure) with the new pediatric formulation.

Children 2-12 years-old have also been included as a target population, to represent those who may have been infected via congenital or vector-borne transmission, and usually present with the early chronic indeterminate form of the disease. In CD endemic countries these groups of children are usually diagnosed through school or community screening programs, and also have a high chance of cure (> 60-75%) with Bz treatment.

Population PK has been chosen as the study design as it would minimise the number of samples per patient, an important requirement for studies conducted in the pediatric population. The dearth of PK data in adults and lack of information on the variability in the target population does not allow for power calculations and the use of optimal sampling design for definition of the timing of samples. Experts reviewed the available information and recommended sparse sampling, with 5 PK samples distributed over the absorption phase (1 sample), steady-state (2 samples) and elimination phase (2 samples). With a total of 5 PK measurements per patient and a total of 80 patients stratified by age, it is expected that PK curves and variability can be drawn with an adequate level of precision.

PK data obtained from this study is expected to inform an age-adapted Bz regimen for the pediatric population affected by CD.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 80
• Est. completion date: October 2012
• Est. primary completion date: August 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 12 Years

Eligibility

Inclusion Criteria:

• Age between newborn (1day) - 12 years

• Diagnosis of T. cruzi infection by:

• Direct microscopic examination or

• Conventional serology, at least two positive tests (ELISA, IIF or HAI)

• Written informed consent form by parent/ legal representative

• Children assent if > 7 years

Exclusion Criteria:

• Pre-term (< 37 weeks gestational age) or weight < 2500 g

• Female subject who has reached menarche

• Subjects presenting any other acute or chronic health conditions, that in the opinion of the PI, may interfere with the PK, efficacy and/or safety evaluation of the study drug

• Known history of hypersensitivity or serious adverse reactions to nitro- imidazoles

• History of CD treatment with benznidazole or nifurtimox in the past

• Immunocompromised patients (clinical history compatible with HIV infection, primary immunodeficiency or prolonged treatment with corticosteroids or other immunosuppressive drugs)

• Abnormal laboratory test values at screening for the following parameters: total WBC count, platelet count, ALT, AST, total bilirubin and creatinine.

Exception for this criterion is considered for newborns with congenital Chagas Disease, for whom ALT/AST and bilirubin will not be considered exclusion criteria unless considered clinically significant by the investigator.

• Inability to comply with follow-up and/or not having a permanent address

• Any condition that prevents the subject from taking oral medication

Related Conditions & MeSH terms

• Chagas Disease
• Chagas' Disease

Intervention

Drug:
• Benznidazole 12,5mg or 100mg
All 80 subjects recruited into the study will receive treatment with: - Benznidazole (Laboratório Farmacêutico do Estado de Pernambuco -LAFEPE - Recife - Brazil; tablet 12.5mg or 100mg), 7.5 mg/Kg/day PO (actual range of 5.5-8.5 mg/Kg/d), divided in two daily doses, for 60 days.

Locations

Country	Name	City	State
Argentina	Hospital General de Niños Ricardo Gutierrez	Buenos Aires
Argentina	Hospital de Niños "Doctor Héctor Quintana"	Jujuy
Argentina	Hospital Público Materno Infantil	Salta

Sponsors (2)

Lead Sponsor	Collaborator
Drugs for Neglected Diseases	LAT Research

Country where clinical trial is conducted

Argentina, 

References & Publications (5)

Andrade AL, Martelli CM, Oliveira RM, Silva SA, Aires AI, Soussumi LM, Covas DT, Silva LS, Andrade JG, Travassos LR, Almeida IC. Short report: benznidazole efficacy among Trypanosoma cruzi-infected adolescents after a six-year follow-up. Am J Trop Med Hyg. 2004 Nov;71(5):594-7. — View Citation

de Andrade AL, Zicker F, de Oliveira RM, Almeida Silva S, Luquetti A, Travassos LR, Almeida IC, de Andrade SS, de Andrade JG, Martelli CM. Randomised trial of efficacy of benznidazole in treatment of early Trypanosoma cruzi infection. Lancet. 1996 Nov 23;348(9039):1407-13. — View Citation

Garcia-Bournissen F, Altcheh J, Giglio N, Mastrantonio G, Della Védova CO, Koren G. Pediatric clinical pharmacology studies in Chagas disease: focus on Argentina. Paediatr Drugs. 2009;11(1):33-7. Review. — View Citation

Ribeiro I, Sevcsik AM, Alves F, Diap G, Don R, Harhay MO, Chang S, Pecoul B. New, improved treatments for Chagas disease: from the R&D pipeline to the patients. PLoS Negl Trop Dis. 2009 Jul 7;3(7):e484. doi: 10.1371/journal.pntd.0000484. Review. — View Citation

Sosa-Estani S, Segura EL. Etiological treatment in patients infected by Trypanosoma cruzi: experiences in Argentina. Curr Opin Infect Dis. 2006 Dec;19(6):583-7. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pharmacokinetics Endpoints	Plasma level concentrations of benznidazol determined in children at first day of treatment (Day 0), steady state phase (D7 and Day 30) and at the end of treatment (Day 60).; Population pharmacokinetics parameters of benznidazole in children, including CL, Vd, and Ka.; Individual AUC.; Individual Cmax.; Individual Cmin.; Individual t1/2 will be estimated using population parameters.	Day 60
Secondary	Efficacy Endpoints	Parasitological cure rate as determined by qualitative PCR at the end of treatment (Day 60).	Day 60
Secondary	Safety endpoints	Rate of Serious of Adverse Events and/or adverse events leading to treatment discontinuation.	Day 60
Secondary	Safety Endpoints	Rate and severity of adverse events.; Covariates to be evaluated: age, gender, weight, height, parasite load at baseline and phase of disease (acute vs chronic).	Day 60

External Links

•   Drugs for Neglected Diseases initiative