Skip to main content
OpenTrials
Completed

NCT Number: NCT04918927

Favipiravir +/- Nitazoxanide: Early Antivirals Combination Therapy in COVID-19

The 2020 pandemic of SARS-CoV-2 causing COVID-19 disease is an unprecedented global emergency. COVID-19 appears to be a disease with an early phase where the virus replicates, coinciding with first presentation of symptoms, followed by a later 'inflammatory' phase which results in severe disease in some individuals. It is known from other rapidly progressive infections such as sepsis and influenza that early treatment with antimicrobials is associated with better outcome. The hypothesis is that this holds for COVID-19 and that early antiviral treatment may prevent progression to the later phase of the disease.

The plan is to conduct a proof-of-principle placebo-controlled clinical trial of favipiravir plus or minus nitazoxanide in health workers, their household members and IMSS beneficiaries. Participants with or without symptomatic COVID-19 or tested positive will be assigned to receive favipiravir plus nitazoxanide or favipiravir plus nitazoxanide placebo. The primary outcome will be the difference in the amount of virus ('viral load') in the upper respiratory tract after 5 days of therapy. Secondary outcomes will include hospitalization, major morbidity and mortality, pharmacokinetics, and impact of antiviral therapy on viral genetic mutation rate.

If favipiravir with nitazoxanide demonstrates important antiviral effects without significant toxicity, there will be a strong case for a larger trial in people at high risk of hospitalization or intensive care admission, for example older patients and/or those with comorbidities and with early disease.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Covid19 COVID-19 Coronaviridae Infections Coronavirus Infections Infections Lung Diseases Nidovirales Infections Pneumonia Pneumonia, Viral RNA Virus Infections Respiratory Tract Diseases Respiratory Tract Infections Virus Diseases

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hospital de Infectología "Daniel Méndez Hernández" del Centro Médico Nacional La Raza

Mexico City, Azcapotzalco, 02290, Mexico

About this study

FANTAZE is a Phase IIA randomised, double-blind, placebo-controlled, interventional trial.Participants will be adults who have developed the early symptoms of COVID-19 within the first 5 days, or tested positive for SARS-CoV-2 within the first 7 days of symptom onset, or not presenting symptoms but tested positive within the last 48 hours (date/time of test must be within 48 hours of enrolment).

Eligible participants will be randomised 1:1 to receive one of the following combinations:

Favipiravir + Nitazoxanide (both active); Favipiravir active + Nitazoxanide placebo;

All participants will be enrolled and followed up for 28 days. A saliva sample for virological analysis and safety blood samples will be collected at baseline, as well as a diagnostic nose and throat swab, if the participant hasn't been tested for COVID-19 yet. Following randomisation, participants will take trial medication for 7 days and during this period will take a daily saliva sample and complete a symptoms diary including four daily temperature measurements.

Participants will have two follow-up visits at Day 7 and Day 14 where they will be assessed and undergo blood tests for toxicity and pharmacokinetic assessment (on Day 7 only) and provide stool samples. Participants will have a telephone follow up three (3) weeks after their last day of treatment (Day 7) and further information will be collected through a questionnaire.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Health workers, their household members and, IMSS beneficiaries with the following:
  • Symptoms compatible with COVID-19 disease (Fever >37.8oC on at least one occasion AND either cough and/ or anosmia) within the first 5 days of symptom onset (date/time of enrolment must be within the first 5 days of symptom onset)
  • OR ANY symptoms compatible with COVID-19 disease (may include, but are not limited to fever, cough, shortness of breath, malaise, myalgia, headache, coryza) and tested positive for SARS-CoV-2 within the first 7 days of symptom onset (date/time of enrolment must be within the first 7 days of symptom onset)
  • OR no symptoms but tested positive for SARS-CoV-2 within the last 48 hours (date/time of test must be within 48 hours of enrolment)
  • Male or female aged 18 years to 70 years old inclusive at screening
  • Willing and able to take daily saliva samples
  • Able to provide full informed consent and willing to comply with trial-related procedures

Exclusion criteria

  • Known hypersensitivity to any of the active ingredients or excipients in favipiravir, and in nitazoxanide and matched placebo
  • Chronic liver disease at screening (known cirrhosis of any aetiology, chronic hepatitis (e.g. autoimmune, viral, steatohepatitis), cholangitis or any known elevation of liver aminotransferases with AST or ALT > 3 X ULN)*
  • Chronic kidney disease (stage 3 or beyond) at screening: eGFR < 60 ml/min/1.73m2*
  • HIV infection, if untreated, detectable viral load or on protease inhibitor therapy
  • Any clinical condition which the investigator considers would make the participant unsuitable for the trial
  • Concomitant medications known to interact with favipiravir, and with nitazoxanide and matched placebo, and carry risk of toxicity for the participant (See Appendix 4)
  • Current severe illness requiring hospitalisation
  • Pregnancy and/ or breastfeeding
  • Eligible female participants of childbearing potential and male participants with a partner of childbearing potential not willing to use highly effective contraceptive measures during the trial and within the time point specified following last trial treatment dose.
  • Participants enrolled in any other interventional drug or vaccine trial (co-enrolment in observational studies is acceptable).
  • Considering the importance of early treatment of COVID-19 to impact viral load, the absence of chronic liver/ kidney disease will be confirmed verbally by the participant during pre- screening and Screening/Baseline visit. Safety blood samples will be collected at Screening/Baseline visit (Day 1) and test results will be examined as soon as they become available within 24 hours.

Treatment and study plan

Favipiravir

Drug

Oral Favipiravir 1800 mg twice daily on Day 1, followed by 400 mg four (4) times daily from Day 2 to Day 7

Nitazoxanide

Drug

Nitazoxanide at 1000 mg twice daily on Day 1 followed by 500 mg four (4) times daily from Day 2 to Day 7

Other names: Daxon

Nitazoxanide Placebo

Other

Nitazoxanide matched placebo at 1000 mg twice daily on Day 1 followed by 500 mg four (4) times daily from Day 2 to Day 7.

Other names: Daxon Placebo

Primary outcomes

  1. Upper respiratory tract viral load at Day 5.

    Time frame: Day 5 from randomisation

    Quantitative polymerase chain reaction (PCR) performed on saliva samples at Day 5 of therapy

Secondary outcomes

  1. Percentage of participants with undetectable upper respiratory tract viral load after 5 days of therapy

    Time frame: Day 5 from randomisation

    Method of measurement: quantitative polymerase chain reaction (PCR) performed on saliva samples.

  2. Proportion of participants with undetectable stool viral load after 7 days of therapy and 14 days post-randomisation.

    Time frame: Day 7 and Day 14 from randomization

    Method of measurement: PCR performed on stool samples

  3. Rate of decrease in upper respiratory tract viral load during 7 days of therapy.

    Time frame: From day of randomisation to day 7

    Method of measurement: PCR performed on daily saliva samples

  4. Duration of fever following commencement of medication

    Time frame: From day of randomisation to day 7

    Methods of measurement: daily body temperature records between Day 1 and Day 7 post-randomisation

  5. Proportion of participants with hepatotoxicity after 7day of therapy and 14 days post-randomisation.

    Time frame: Day 7 and day 14 from randomisation.

    Method of measurement: standard diagnostic laboratory assays for liver transaminases, alkaline phosphatase and bilirubin.

  6. Proportion of participants with other medication-related toxicity after 7 days of therapy and 14 days post-randomisation.

    Time frame: Day 7 and Day 14 from randomisation.

    Methods of measurement: determination of medication-related adverse events by investigators.

  7. Proportion of participants admitted to hospital with COVID-19 related illness.

    Time frame: 28 days from randomisation.

    Methods of measurement: participant self-report, review of hospital records and discharge summaries

  8. Proportion of participants admitted to ICU with COVID-19 related illness.

    Time frame: 28 days from randomisation.

    Methods of measurement: participant self-report, review of hospital records and discharge summaries.

  9. Proportion of participants who have died with COVID-19 related illness

    Time frame: 28 days from randomisation.

    Methods of measurement: next of kin report, review of hospital records and discharge summaries.

  10. Pharmacokinetic analysis of favipiravir and tizoxanide: Clearance (CL)

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the following primary PK parameter: Clearance (CL).

  11. Pharmacokinetic analysis of favipiravir and tizoxanide: Volume of distribution (V)

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the following primary PK parameter: Volume of distribution (V),

  12. Pharmacokinetic analysis of favipiravir and tizoxanide: Absorption rate constant (Ka)

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the following primary PK parameter: Absorption rate constant (Ka).

  13. Pharmacokinetic analysis of favipiravir and tizoxanide: Maximum concentration (Cmax)

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the previous described primary PK parameters from which the following secondary parameter will be derived: Maximum concentration (Cmax),

  14. Pharmacokinetic analysis of favipiravir and tizoxanide: Time to maximum concentration (Tmax)

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the previous described primary PK parameters from which the following secondary parameter will be derived: Time to maximum concentration (Tmax),

  15. Pharmacokinetic analysis of favipiravir and tizoxanide: Elimination rate constant (Ke)

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the previous described primary PK parameters from which the following secondary parameter will be derived: Elimination rate constant (Ke),

  16. Pharmacokinetic analysis of favipiravir and tizoxanide: Area Under the Curve extrapolated to infinity (AUC 80-inf).

    Time frame: Day 7 from randomization

    Methods of measurement: assay of favipiravir and tizoxanide levels in plasma at Day 7 of therapy. All participants from each arm will provide a pre-dose sample and two post-dose (30 to 60 min) samples on Day 7 of therapy. A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic data.

    The model will estimate the previous described primary PK parameters from which the following secondary parameter will be derived:

    Area Under the Curve extrapolated to infinity (AUC 80-inf)),

  17. Pharmacodynamic analysis of favipiravir and tizoxanide: Rate of viral load decline (delta)

    Time frame: Day 7 from randomization

    A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic and viral load (pharmacodynamic) data.

    The model will estimate the following pharmacodynamic parameter: Rate of viral decline (delta) Maximum increase in viral load under drug treatment (Emax), Concentration to achieve half the maximum possible effects (EC50)

  18. Pharmacodynamic analysis of favipiravir and tizoxanide: Maximum increase in viral load under drug treatment (Emax).

    Time frame: Day 7 from randomization

    A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic and viral load (pharmacodynamic) data.

    The model will estimate the following pharmacodynamic parameter: Maximum increase in viral load under drug treatment (Emax).

  19. Pharmacodynamic analysis of favipiravir and tizoxanide: Concentration to achieve half the maximum possible effects (EC50)

    Time frame: Day 7 from randomization

    A nonlinear mixed effects model will be fitted jointly to favipiravir and tizoxanide pharmacokinetic and viral load (pharmacodynamic) data.

    The model will estimate the following pharmacodynamic parameter: Concentration to achieve half the maximum possible effects (EC50)

  20. Exploratory: proportion of participants with deleterious or resistance-conferring mutations in SARS-CoV-2.

    Time frame: Day 7 from randomization

    Method of measurement: deep sequencing of virus and bioinformatic analysis.

Sponsors and collaborators

Lead sponsor

Coordinación de Investigación en Salud, Mexico

Other Gov

Collaborators

  • Centro de Investigacion y Estudios Avanzados del Instituto Politecnico Nacional (CINVESTAV)
  • Hakken Enterprise
  • Siegfried Rhein S.A. de C.V.
  • Strides Pharma Science Limited
  • Univeridad Autonoma de Guadalajara
  • University College, London

Registry information

Official study title

Favipiravir and/or Nitazoxanide: a Randomized, Double-blind, Placebo-controlled Trial of Early Antiviral Therapy in COVID-19 (FANTAZE)

Acronym: FANTAZE

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jun 9, 2021
Registry last updated
Mar 24, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.