Study to Evaluate Fexinidazole Dosing Regimens for the Treatment of Adult Patients With Chagas Disease

NCT ID: NCT02498782

Last Updated: 2015-07-15

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 140 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-07-31
• Study Completion Date: 2016-02-29

Brief Summary

The hypothesis is to evaluate if the treatment with Fexinidazole will lead to a better sustained clearance of the parasites at 6 months of follow-up when in comparison to placebo in patients with chronic indeterminate CD.

Detailed Description

Chagas Disease (CD) ranks among the world's most neglected diseases. In Latin America, 21 countries are endemic for CD with an estimated 100 million people at risk of contracting the disease. Estimates from the 1980s indicated that some 16 million to 18 million individuals were infected. In the 1990s, after a series of multinational control initiatives, estimates of the number of infected people were revised to 9.8 million in 2001. The estimated burden of disease in terms of disability-adjusted life years (DALYs) declined from 2.7 million in 1990 to 586,000 in 2001. Recent estimates from PAHO (2006) indicate 7.54 million infected people and 55,185 new cases per year. New safe and effective treatments for Chagas Disease are urgently needed. Current chemotherapy options for CD have significant limitations, including long treatment durations, and safety and tolerability concerns. For many years, inhibitors of the sterol biosynthesis pathway, such as posaconazole and ravuconazole, were considered as the most promising new drugs candidates for Chagas Disease. Following the recent results of CHAGAZASOL, an investigator-initiated trial conducted in Barcelona, where a high recrudescence rate was observed in the posaconazole treatment arms (80-90%, versus 5% in the benznidazole arm), there is increased concern on the future of the class. Nitroimidazoles are a well-known class of pharmacologically active compounds, among which several have shown good activity against trypanosomes. While concerns over mutagenicity and safety have mitigated their potential as drug candidates, several members of this family are widely used as antibiotics, indicating that it is possible to select compounds with acceptable activity/toxicity profile in this class. Fexinidazole had been in preclinical development as a broad-spectrum antiprotozoal drug by Hoechst in the 1970s-1980s, but its clinical development was not pursued at the time. The molecule was ''rediscovered'' and selected for development by the Drugs for Neglected Diseases initiative (DNDi) as a new drug candidate for sleeping sickness, following a systematic review and profiling of more than 700 nitroheterocyclic compounds (mostly nitroimidazoles) from diverse sources, which included assessments of antiparasitic activity and mutagenic potential. Fexinidazole underwent extensive regulatory toxicology studies, including safety pharmacology (respiratory, cardiovascular, and general behaviour) and 4 weeks of repeated dose toxicokinetics studies in rat and dogs. 90-day toxicology studies were performed by Hoechst, allowing validation of the 3 months dosing in rat to a dose of 800 mg/kg/day and dog up to 125 mg/kg/day. Overall, Fexinidazole was found to be well tolerated, with no specific toxicity or other concerns.

During 2010-2011, DNDi carried out several Phase I clinical trials assessing the safety and pharmacokinetics of Fexinidazole in human volunteers given in single and multiple doses. A pivotal phase II/III clinical safety and efficacy study in sleeping sickness patients was started in 2012 and to-date shows encouraging safety and tolerability profile and exposure in patients.

Fexinidazole has previously been described as effective and superior to benznidazole or nifurtimox in one acute murine infection model with the T. cruzi Brazil 32 strain, but the methodologies used to establish cure are no longer considered the most accurate. More recently, in vitro studies performed at Institute Pasteur Korea (IPK) showed that Fexinidazole parent and metabolites (M1 and M2) are more or less equipotent versus T. cruzi in vitro (Tulahuen strain). Fexinidazole Sulfone (M2) is potent against a panel of T. cruzi strains (not including Colombiana or VL-10) albeit at higher concentrations than Benznidazole (2 to 4-fold). Fexinidazole Sulfone requires 72 to 96 hrs exposure at concentrations at or above 100 mM (31 mg/ml) with the Y strain; Benznidazole exhibits the same kinetics but requires exposure at the lower concentration of 12.5 mM (3.3 mg/ml).

Conditions

Chagas Disease; Trypanosomiasis, South American; South American Trypanosomiasis; Disease, Chagas

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Fexinidazole, 1800 mg, 2 weeks

1800mg (High Dose) 2 weeks (HD - 2 weeks) Group: Fexinidazole, 1800 mg QD for 2 weeks, followed by placebo to complete 8 weeks (total dose: 25,2 g)

Group Type: ACTIVE_COMPARATOR

Fexinidazole

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Fexinidazole, 1800 mg, 4 weeks

1800mg (High Dose) 4 weeks (HD - 4 weeks) Group: Fexinidazole, 1800 mg QD for 4 weeks, followed by placebo to complete 8 weeks (total dose: 50,4 g)

Group Type: ACTIVE_COMPARATOR

Fexinidazole

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Fexinidazole, 1800 mg, 8 weeks

1800mg (High Dose) 8 weeks (HD - 8 weeks) Group: Fexinidazole, 1800 mg QD, for 8 weeks (total dose: 100,8 g)

Group Type: ACTIVE_COMPARATOR

Fexinidazole

Intervention Type: DRUG

Fexinidazole, 1200 mg, 2 weeks

1200mg (Dose 2 weeks) 2 weeks (LD - 2 weeks) Group: Fexinidazole, 1200 mg QD for 2 weeks, followed by placebo to complete 8 weeks (total dose: 16,8 g)

Group Type: ACTIVE_COMPARATOR

Fexinidazole

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Fexinidazole, 1200 mg, 4 weeks

1200mg (Low Dose) 4 weeks (LD - 4 weeks) Group: Fexinidazole, 1200 mg QD for 4 weeks, followed by placebo to complete 8 weeks (total dose: 33,6 g)

Group Type: ACTIVE_COMPARATOR

Fexinidazole

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Fexinidazole, 1200 mg, 8 weeks

1200mg (Low Dose) 8 weeks (LD - 8 weeks) Group: Fexinidazole, 1200 mg QD for 8 weeks (total dose: 67,2 g)

Group Type: ACTIVE_COMPARATOR

Fexinidazole

Intervention Type: DRUG

Placebo

Placebo (8 weeks) Group: Fexinidazole matched placebo tablets QD for 8 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Interventions

Fexinidazole

Intervention Type: DRUG

Placebo

Intervention Type: DRUG

Other Intervention Names

1Himidazole,1methyl2[4methylthio)phenoxymethyl] 5nitroimidazole

Eligibility Criteria

Inclusion Criteria

• Confirmed diagnosis of T. cruzi infection by Serial qualitative PCR (three samples collected over a single day, at least one of which must be positive) AND Conventional serology (a minimum of two out of three positive tests must be positive [Conventional ELISA, Recombinant Elisa or IIF)
• Women in reproductive age must have a negative serum pregnancy test at screening, must not be breastfeeding, and consistently use a highly effective contraceptive method during the entire trial.
• Normal EKG (PR ≤200 msec, QRS ≤120 msec, and QTc ≥400msec and ≤450 msec interval durations) at screening

Exclusion Criteria

• Signs and/or symptoms of chronic cardiac and/or digestive form of CD (as per Study Manual of Operations)
• History of cardiomyopathy, heart failure or ventricular arrhythmia
• Any other acute or chronic health conditions that, in the opinion of the PI, may interfere with the efficacy and/or safety evaluation of the study drug (such as acute infections, history of HIV infection, diabetes, liver and renal disease requiring medical treatment)
• Laboratory test values considered clinically significant or out of the allowable range at screening as follows:

• Total WBC must be within the normal range, with an acceptable margin of +/- 5% (3,800 - 10,500 / mm3).
• Platelets must be within the normal range up to 550,000 / mm3
• Total bilirubin must be within the normal range Transaminases (ALT and AST) must be within the normal range, with an acceptable margin of 25% above the upper limit of normality (ULN), < 1.25 x ULN.
• Creatinine must be within an acceptable margin of 10% above the ULN, <1.10 x ULN.
• Alkaline phosphatase must be within the normal range up to Grade 1 CTCAE (< 2.5 x ULN)
• GGT must be within the normal range up to 2x ULN.
• Potassium, Magnesium, Calcium must be within the normal range
• History of alcohol abuse or any other drug addiction (as specified in the Study Manual of Operations).
• Any condition that prevents the patient from taking oral medication.
• Patients with contra-indication (known hypersensitivity) to other nitroimidazoles, e.g. metronidazole.
• Any concomitant use of antimicrobial or anti-parasitic agents.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Drugs for Neglected Diseases

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Faustino Torrico, MD

Role: PRINCIPAL_INVESTIGATOR

Plataforma de Antención Integral de Pacientes con Enfermedad de Chagas, Cochabamba, Bolivia

Joaquim Gascón, MD

Role: PRINCIPAL_INVESTIGATOR

Centro de Salud Internacional, Hospital Clínico de Barcelona

Lourdes O Daza, MD

Role: PRINCIPAL_INVESTIGATOR

Plataforma de Antención Integral de Pacientes con Enfermedad de Chagas, Tarija, Bolivia

Locations

Plataforma Atención Integral de Pacientes con Enfermedad de Chagas

Cochabamba, , Bolivia

Site Status: RECRUITING

Plataforma de Atención Integral de Pacientes con Enfermedad de Chagas

Tarija, , Bolivia

Site Status: RECRUITING

Countries

Bolivia

Central Contacts

Isabela Ribeiro, MD

Role: CONTACT

iribeiro@dndi.org

+552125290400

Fabiana BS Rocha, MD

Role: CONTACT

fbarreira@dndi.org

+552125290400 ext. 0416

Facility Contacts

Faustino Torrico, MD

Role: primary

foxtorrico@yahoo.com

59177411905

Cristina Alonso, MD

Role: backup

calonso@dndi.org

59172211312

Lourdes O Daza, MD

Role: primary

lourdesortizd@yahoo.es

5916672252

Erika Ribeiro, Pharm D

Role: backup

ecorreia@dndi.org

59175969924

References

Torrico F, Gascon J, Ortiz L, Pinto J, Rojas G, Palacios A, Barreira F, Blum B, Schijman AG, Vaillant M, Strub-Wourgaft N, Pinazo MJ, Bilbe G, Ribeiro I. A Phase 2, Randomized, Multicenter, Placebo-Controlled, Proof-of-Concept Trial of Oral Fexinidazole in Adults With Chronic Indeterminate Chagas Disease. Clin Infect Dis. 2023 Feb 8;76(3):e1186-e1194. doi: 10.1093/cid/ciac579.

Reference Type: DERIVED

PMID: 35925555 (View on PubMed)

Other Identifiers

DNDi-CH-FEXI-001

Identifier Type: -

Identifier Source: org_study_id