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Status unknownNCT02498782Updated Jul 15, 2015

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

A Phase 2 interventional study of Fexinidazole and Placebo in Chagas Disease, Trypanosomiasis, South American and South American Trypanosomiasis, sponsored by Drugs for Neglected Diseases. Status unknown at 2 sites in Bolivia. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2015-07-15.

Sponsored by Drugs for Neglected Diseases · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jul 2015), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
140
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study 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.

Read the 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).

02

Conditions studied

  • Chagas Disease
  • Trypanosomiasis, South American
  • South American Trypanosomiasis
  • Disease, Chagas

Keywords

  • Chagas Disease
  • Dosage forms
  • Regimens
03

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
140 participants (estimated)

Study arms

  • Active comparator
    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)

    Drug: Fexinidazole · Drug: Placebo

  • Active comparator
    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)

    Drug: Fexinidazole · Drug: Placebo

  • Active comparator
    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)

    Drug: Fexinidazole

  • Active comparator
    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)

    Drug: Fexinidazole · Drug: Placebo

  • Active comparator
    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)

    Drug: Fexinidazole · Drug: Placebo

  • Active comparator
    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)

    Drug: Fexinidazole

  • Placebo comparator
    Placebo

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

    Drug: Placebo

Interventions

  • DrugFexinidazole

    Also known as: 1Himidazole,1methyl2[4methylthio)phenoxymethyl] 5nitroimidazole

  • DrugPlacebo
05

What researchers measure

Primary outcomes

  1. Parasitological cure rate (PCR)

    Parasitological cure rate as determined by serial negative qualitative PCR results (3 negative PCR results, from 3 samples to be collected in the same day) at end of treatment (8 weeks) and sustained parasitological clearance until 6 months follow-up.

    Time frame: 8 weeks and sustained until 6 months

  2. Adverse events

    Incidence and severity of adverse events (clinical, laboratory and EKG)

    Time frame: 7 months

  3. Serious Adverse events

    Incidence of Serious Adverse Events and/or adverse events leading to treatment discontinuation

    Time frame: 7 months

Secondary outcomes

  1. Parasite Clearance (qualitative PCR)

    Parasite clearance at weeks 2, 3, 4, 6, 10, and at 4 and 6 months follow-up as measured by qualitative PCR

    Time frame: weeks 2, 3, 4, 6, 10, and at 4 and 6 months follow-up

  2. Parasite load

    Change in parasite load over time assessed at weeks 2, 3, 4, 6, 10, and at 4 and 6 months follow-up as measured by quantitative PCR

    Time frame: weeks 2, 3, 4, 6, 10 and 4 and 6 months

  3. Serological response

    Serological response (conventional and non-conventional serologies) (incidence of conversion to negative and changes in titers over time) assessed at week 10 and at 4 and 6 months follow-up.

    Time frame: week 10, 4 and 6 months

  4. Blood culture for parasite genotyping

    Blood culture and in vitro drug and susceptibility testing of isolated parasite strains at 6 months.

    Time frame: 6 months

Other outcomes

  1. Plasma level concentrations

    Plasma level concentrations of Fexinidazole and its metabolites M1 (sulfoxide) and M2 (sulfone) will be determined at D0 (pre-dose), at randomly selected time after first day of treatment administration (day 1, post-dose), at steady-state phase (week 2-9), and at week 10

    Time frame: D0 (pre-dose), at randomly selected time at day 1, post-dose, at steady-state phase (week 2-9), and at week 10

06

Study locations

2 of 2 sites recruiting
  • Plataforma Atención Integral de Pacientes con Enfermedad de Chagas
    Cochabamba, Bolivia
    • Faustino Torrico, MD · Contact · foxtorrico@yahoo.com · 59177411905
    • Cristina Alonso, MD · Contact · calonso@dndi.org · 59172211312
    • Faustino Torrico, MD · Principal investigator
    Recruiting
  • Plataforma de Atención Integral de Pacientes con Enfermedad de Chagas
    Tarija, Bolivia
    Recruiting
07

Registry details

Key details

Study ID
NCT02498782
Lead sponsor
Drugs for Neglected Diseases
Responsible party
Sponsor
First posted
Jul 15, 2015
Start date
Jul 2014
Primary completion
Sep 2015 (estimated)
Completion
Feb 2016 (estimated)
Last update
Jul 15, 2015

Study contacts

Isabela Ribeiro, MD
Contact
iribeiro@dndi.org
+552125290400
Fabiana BS Rocha, MD
Contact
fbarreira@dndi.org
+552125290400 ext. 0416
Faustino Torrico, MD
principal investigator · Plataforma de Antención Integral de Pacientes con Enfermedad de Chagas, Cochabamba, Bolivia
Joaquim Gascón, MD
principal investigator · Centro de Salud Internacional, Hospital Clínico de Barcelona
Lourdes O Daza, MD
principal investigator · Plataforma de Antención Integral de Pacientes con Enfermedad de Chagas, Tarija, Bolivia

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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