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Hydroxychloroquine and Nitazoxanide Combination Therapy for COVID-19

Primary Purpose

COVID-19

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Hydroxychloroquine plus Nitazoxanide
Standard care
Sponsored by
Tanta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 focused on measuring Hydroxychloroquine, Nitazoxanide, COVID-19

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Confirmed cases of COVID-19 (Positive RT-PCR)
  • Newly diagnosed symptomatic patients.
  • Adults (18-65 Years old)
  • Both sexes

Exclusion Criteria:

  • Patients with abnormal liver function (ALT, AST), chronic kidney disease or dialysis (CrCl< 30 ml/min)
  • Pregnant women or women who are breastfeeding
  • Immunocompromised patients taking medication upon screening
  • Subjects with comorbid condition like hypertension, cardiovascular disease, diabetes mellites, asthma, COPD, malignancy
  • Patients having allergy to Hydroxychloroquine and/or Nitazoxanide
  • Patients with contraindication towards the study medication including retinopathy, G6PD deficiency and QT prolongation.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Hydroxychloroquine plus Nitazoxanide

    Standard care

    Arm Description

    200 mg of Hydroxychloroquine orally three times daily for 10 days plus 500 mg of Nitazoxanide orally twice daily for 6 days

    Standard care delivered in the COVID-19 isolation hospitals.

    Outcomes

    Primary Outcome Measures

    Number of patients with COVID-19-negative PCR
    PCR analysis of COVID-19 RNA in patients

    Secondary Outcome Measures

    Number of patients with improved respiratory rate
    improved breaths per minute for the patients
    Number of patients with improved PaO2
    Change in PaO2 in mmHg of the patients
    Number of patients with normalized Serum IL6
    Serum IL6 in pg/mL of the patients
    Number of patients with normalized Serum TNFα
    Serum TNFα in pg/mL of the patients
    Number of patients with normalized Serum iron
    Serum iron in microgram/dL of the patients
    Number of patients with normalized Serum ferritin
    Serum ferritinin microgram/L of the patients
    Number of patients with normalized International normalized ratio "INR" for prothrombin time
    International normalized ratio "INR" for prothrombin time of 2
    Number of patients with normalized complete blood count "CBC"
    CBC for lymphocyte count in cells/microliter
    The Mortality rate among treated patients
    Mortality rate [number of dead patients/total number of treated patients]

    Full Information

    First Posted
    April 18, 2020
    Last Updated
    April 22, 2020
    Sponsor
    Tanta University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04361318
    Brief Title
    Hydroxychloroquine and Nitazoxanide Combination Therapy for COVID-19
    Official Title
    Clinical Trial Evaluating Safety and Efficacy of Hydroxychloroquine and Nitazoxanide Combination as Adjuvant Therapy in Covid-19 Newly Diagnosed Egyptian Patients: A Tanta University Hope
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    May 2020 (Anticipated)
    Primary Completion Date
    October 2020 (Anticipated)
    Study Completion Date
    December 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Tanta University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    In December 2019, a new infectious respiratory disease emerged in Wuhan, Hubei province, China. An initial cluster of infections was linked to Huanan seafood market, potentially due to animal contact. Subsequently, human-to-human transmission occurred and the disease, now termed coronavirus disease 19 (COVID-19) rapidly spread within China and all over the world. A novel coronavirus, SARS-coronavirus 2 (SARS-CoV-2), which is closely related to SARS-CoV, was detected in patients and is believed to be the etiologic agent of the new lung disease. The causative agent of the current COVID-19 pandemic, SARS-CoV-2, is a single stranded positive sense RNA virus that is closely related to severe acute respiratory syndrome coronavirus (SARS-CoV).
    Detailed Description
    Selected Drugs Hydroxychloroquine (an analog of chloroquine) has been demonstrated to have an anti-SARS-CoV activity in vitro. Hydroxychloroquine clinical safety profile is better than that of chloroquine (during long-term use) and allows higher daily dose and has fewer concerns about drug-drug interactions. Hydroxychloroquine has long-term safety (600 mg/day for 12 to 18 months was safe). Hydroxychloroquine effectively inhibited both the entry, transport and the post-entry stages of SARS-CoV-2, similar to the chloroquine, and one study found Hydroxychloroquine to be a more potent agent than chloroquine in inhibiting SARS-CoV-2 in vitro. Hydroxychloroquine acts as a weak base that can change the pH of acidic intracellular organelles including endosomes/lysosomes, essential for the membrane fusion. Besides, the significant decrease in the production of pro-inflammatory markers and cytokines with Hydroxychloroquine has made this agent a successful disease modifying anti-inflammatory agent in the treatment of various autoimmune diseases. An additional issue to be considered in severely sick patients is cytokine storm associated with disease severity of SARS-CoV-2. There are no currently available data from randomized clinical trials (RCTs) to inform clinical guidance on the use, dosing, or duration of Hydroxychloroquine for prophylaxis or treatment of SARS-CoV-2 infection. Although optimal dosing and duration of Hydroxychloroquine for treatment of COVID-19 are unknown, some U.S. clinicians have reported anecdotally different Hydroxychloroquine dosing such as 400 mg twice daily on day one, then daily for 5 days; 400 mg twice daily on day one, then 200 mg twice daily for 4 days; 600 mg twice daily on day one, then 400 mg daily on days 2-5. In a recent clinical trial, Hydroxychloroquine sulfate 200 mg, three times per day during ten days was used in patients with COVID-19. Nitazoxanide is originally developed as an antiprotozoal agent and has a broad-spectrum antiviral activity undergoing development for the treatment of influenza and other viral respiratory infections. In addition to its antiviral activity, Nitazoxanide inhibits the production of pro-inflammatory cytokines TNF-α, IL-2, IL-4, IL-5, IL-6, IL-8 and IL-10 in peripheral blood mononuclear cells. Nitazoxanide could improve outcomes in patients infected with MERS-CoV by suppressing overproduction of pro-inflammatory cytokines, including IL-6. Nitazoxanide has been tested in clinical setting for the treatment of acute uncomplicated influenza, where the subjects received either 600 or 300 mg of Nitazoxanide or placebo orally twice daily for five days and were followed for 28 days. Subjects who received Nitazoxanide 600 mg twice daily experienced shorter times to alleviation of symptoms compared with subjects who received 300 mg Nitazoxanide twice daily, which in turn, was shorter than placebo. According to the National Health Commission of the People's Republic of China, there is lack of effective antiviral therapy against COVID-19. Nearly all patients who suffered from COVID-19-associated pneumonia accepted oxygen therapy and WHO recommended extracorporeal membrane oxygenation (ECMO) to patients with refractory hypoxemia. Rescue treatment with convalescent plasma and immunoglobulin G are delivered to some critical cases according to their condition. The rationale of the use of Hydoxychloroquine and Nitazoxanide combination for treatment of COVID-19 infected patients is based on the antiviral and anti-inflammatory activity of the selected drugs. Since the two drugs exhibit different modes of action, it would be of value in containing the viral infection through targeting different sites in the pathophysiology of the disease. Diagnostic criteria The viral research institution in China has conducted preliminary identification of the SARS-CoV-2 through the classical Koch's postulates and observing its morphology through electron microscopy. So far, the golden clinical diagnosis method of COVID-19 is nucleic acid detection in the nasal and throat swab sampling or other respiratory tract samplings by real-time PCR and further confirmation by next-generation sequencing. Side effects of Hydroxychloroquine The most common adverse effects are mild nausea and occasional stomach cramps with mild diarrhea, reduced appetite and vomiting The most serious adverse effects are retinopathy and heart problems Long term use may cause liver toxicity Contraindications of Hydroxychloroquine Heart conditions, diabetes or psoriasis. The drug transfers into breast milk so should be used with care by pregnant or nursing women Interactions of Hydroxychloroquine Antacids may decrease the absorption of Hydroxychloroquine. Both neostigmine and pyridostigmine antagonize the action of Hydroxychloroquine. There may be a link between Hydroxychloroquine and hemolytic anemia in those with glucose-6-phosphate dehydrogenase deficiency. Digoxin; concomitant administration with Hydroxychloroquine may result in increased serum digoxin levels. Insulin or antidiabetic drugs; concomitant administration with Hydroxychloroquine may enhance the effects of the hypoglycemic treatment. Hydroxychloroquine prolongs the QT interval and may increase the risk of inducing ventricular arrhythmias if used concurrently with other arrhythmogenic drugs. Mefloquine and other drugs that lower the convulsive threshold, when co-administered with Hydroxychloroquine, there may be an increased risk of convulsions. Concurrent use of Hydroxychloroquine with antiepileptics may impair the antiepileptic activity. Cyclosporin when used concomitantly with Hydroxychloroquine, an increased plasma cyclosporin level was reported. Side effects of Nitazoxanide The most common adverse effects are GIT as nausea and occasional stomach cramps with mild diarrhea, reduced appetite and vomiting. Nervous system side effects as headache, dizziness, somnolence, insomnia, tremor, and hypesthesia have been reported in less than 1% of the patients. Contraindications of Nitazoxanide There are no data on the excretion of Nitazoxanide into human milk. The manufacturer recommends that caution be used when administering Nitazoxanide to nursing women. Tizoxanide (the active metabolite of Nitazoxanide) is highly bound to plasma protein (> 99.9%). Therefore, it is necessary to monitor for adverse reactions when administering Nitazoxanide concurrently with other highly plasma protein-bound drugs with narrow therapeutic indices, as competition for binding sites may occur (e.g., warfarin). Warning Nitazoxanide should be used with caution in patients with significant renal and hepatic impairment. Research Objectives The pandemic disease COVID-19 is particularly of major importance in Egypt where a heavy population lives. There is an acute need for comprehensive, continuous, and cost-effective health care delivery for infected people. Early detection and strategies for prevention of progression of COVID-19 would make a major difference for these patients and would also be economically beneficial for a resource-constrained country. This research proposal was employed as a practical strategy for providing a suitable drug combination for possible treatment of COVID-19 infected patients. This drug combination may help to prevent the progression of respiratory complications. This can be achieved through different goals as follows: Screening of different drugs related to different pharmacological classes depending on its possible activity against COVID-19 virus. Providing cost-effective and easy-to-implement treatment strategy for infected patients and/or patients with high risk of developing respiratory failure. Finally, this clinical strategy remains an important goal in improving the Egyptian health state which can save people life and save a lot of money. Scope of Work The scope of work will be conducted through: Use of new drug combination of Hydroxychloroquine and Nitazoxanide for treatment of COVID-19 infected people. Since the two drugs exhibit different modes of action, it would be of value in containing the viral infection through targeting different sites in the pathophysiology of the disease. Evaluation of the effect of new drug combination on the symptomatic treatment of newly diagnosed COVID-19 patients through a clinical trial designed according to WHO (clinical management of severe acute respiratory infection (SARI) when COVID-19 disease is suspected) interim guidance published at 13 March 2020. Investigating the impact of new drug combination on the prevention of severe compilations such as acute respiratory distress syndrome (ARDS).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    COVID-19
    Keywords
    Hydroxychloroquine, Nitazoxanide, COVID-19

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare Provider
    Masking Description
    a double blind randomized controlled parallel study
    Allocation
    Randomized
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Hydroxychloroquine plus Nitazoxanide
    Arm Type
    Experimental
    Arm Description
    200 mg of Hydroxychloroquine orally three times daily for 10 days plus 500 mg of Nitazoxanide orally twice daily for 6 days
    Arm Title
    Standard care
    Arm Type
    Active Comparator
    Arm Description
    Standard care delivered in the COVID-19 isolation hospitals.
    Intervention Type
    Combination Product
    Intervention Name(s)
    Hydroxychloroquine plus Nitazoxanide
    Other Intervention Name(s)
    drug therapy
    Intervention Description
    Both hydroxychloroquine & nitazoxanide will be administered orally to participating patients
    Intervention Type
    Other
    Intervention Name(s)
    Standard care
    Intervention Description
    Oxygen administered via ventilator. In addition, antipyretic "paracetamol" may be added if necessary
    Primary Outcome Measure Information:
    Title
    Number of patients with COVID-19-negative PCR
    Description
    PCR analysis of COVID-19 RNA in patients
    Time Frame
    within 10 days to become PCR negative
    Secondary Outcome Measure Information:
    Title
    Number of patients with improved respiratory rate
    Description
    improved breaths per minute for the patients
    Time Frame
    within 30 days
    Title
    Number of patients with improved PaO2
    Description
    Change in PaO2 in mmHg of the patients
    Time Frame
    within 30 days
    Title
    Number of patients with normalized Serum IL6
    Description
    Serum IL6 in pg/mL of the patients
    Time Frame
    within 30 days
    Title
    Number of patients with normalized Serum TNFα
    Description
    Serum TNFα in pg/mL of the patients
    Time Frame
    within 30 days
    Title
    Number of patients with normalized Serum iron
    Description
    Serum iron in microgram/dL of the patients
    Time Frame
    within 30 days
    Title
    Number of patients with normalized Serum ferritin
    Description
    Serum ferritinin microgram/L of the patients
    Time Frame
    within 30 days
    Title
    Number of patients with normalized International normalized ratio "INR" for prothrombin time
    Description
    International normalized ratio "INR" for prothrombin time of 2
    Time Frame
    within 30 days
    Title
    Number of patients with normalized complete blood count "CBC"
    Description
    CBC for lymphocyte count in cells/microliter
    Time Frame
    within 30 days
    Title
    The Mortality rate among treated patients
    Description
    Mortality rate [number of dead patients/total number of treated patients]
    Time Frame
    within 30 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Confirmed cases of COVID-19 (Positive RT-PCR) Newly diagnosed symptomatic patients. Adults (18-65 Years old) Both sexes Exclusion Criteria: Patients with abnormal liver function (ALT, AST), chronic kidney disease or dialysis (CrCl< 30 ml/min) Pregnant women or women who are breastfeeding Immunocompromised patients taking medication upon screening Subjects with comorbid condition like hypertension, cardiovascular disease, diabetes mellites, asthma, COPD, malignancy Patients having allergy to Hydroxychloroquine and/or Nitazoxanide Patients with contraindication towards the study medication including retinopathy, G6PD deficiency and QT prolongation.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Kamal Okasha, MD, PhD
    Phone
    +201004706770
    Email
    vp_research@unv.tanta.edu.eg
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Kamal Okasha, MD, PhD
    Organizational Affiliation
    Tanta University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    Hydroxychloroquine and Nitazoxanide Combination Therapy for COVID-19

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