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Efficacy of Aerosol Combination Therapy of 13 Cis Retinoic Acid and Captopril for Treating Covid-19 Patients Via Indirect Inhibition of Transmembrane Protease, Serine 2 (TMPRSS2)

Primary Purpose

Covid19

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Aerosolized 13 cis retinoic acid plus Inhalation administration by nebulization captopril 25mg
Drug: Standard treatment Standard treatment
Sponsored by
Kafrelsheikh University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Covid19

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Adult SARI patients with 2019-ncov infection confirmed by PCR; Absolute value of lymphocytes < 0. 6x 109/L; Severe respiratory failure within 48 hours and requires admission to ICU. (severe respiratory failure was defined as PaO2/FiO2 < 200 mmHg and was supported by positive pressure mechanical ventilation (including non-invasive and invasive mechanical ventilation, PEEP>=5cmH2O))

Exclusion Criteria:

Age < 18 Pregnant Allergic to experimental drugs and patients have the following conditions:

  • Hypercholesterolemia
  • Hypertriglyceridemia
  • Liver disease
  • Renal disease
  • Sjögren syndrome
  • Pregnancy
  • Lactation
  • Depressive disorder
  • Body mass index less than 18 points or higher than 25 points
  • Contraindications for hormonal contraception or intrauterine device.
  • Autoimmune diseases A history of organ, bone marrow or hematopoietic stem cell transplantation
  • Patients receiving anti-hcv treatment
  • Permanent blindness in one eye
  • History of iritis, endophthalmitis, scleral inflammation or retinitis 15-90 days of retinal detachment or eye surgery
  • History of ACE-inhibitor allergy
  • History of angio-oedema
  • Co-infection with another respiratory pathogen which could be responsible of pneumonia
  • Hypersensitivity to captopril, to any other angiotensin converting enzyme inhibitor or any of the excipients of the specialty used
  • Shock requiring vasopressor infusion
  • Patient on state medical ai
  • The competent physician considered it inappropriate to participate in the study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Sham Comparator

    Arm Label

    Aerosolized 13 cis retinoic acid plus Inhalation administration by nebulization captopril 25mg

    The standard therapy

    Arm Description

    Infected patients will receive aerosolized 13 cis retinoic acid in gradual one dose per day increases from 0.2 mg/kg/day to 4 mg/kg/day as inhaled 13 cis retinoic acid therapy for 14 days plus Inhalation administration by nebulization captopril 25mg for 14 days

    infected patients will receive the standard therapy for COVID-19 for 14 days

    Outcomes

    Primary Outcome Measures

    lung injury score
    Proportion of lung injury score decreased or increased after treatmen

    Secondary Outcome Measures

    Transe membrane protease ,serine II (TMPRSS2) changes over time
    Testosterone levels changes over time
    Dihydrotestosterone(DHT) levels changes over time
    Cholesterol levels changes over time
    Angiotensin 1-7 (Ang 1-7) changes over time
    Angiotensin 1-5 (Ang 1-5) changes over time
    Renin changes over time
    Aldosterone changes over time
    Angiotensin-converting enzyme (ACE) changes over time
    Time to first negative SARS-CoV-2 PCR in NP swap
    All cause mortality rate
    Ventilation free days
    ICU free days

    Full Information

    First Posted
    October 4, 2020
    Last Updated
    October 23, 2020
    Sponsor
    Kafrelsheikh University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04578236
    Brief Title
    Efficacy of Aerosol Combination Therapy of 13 Cis Retinoic Acid and Captopril for Treating Covid-19 Patients Via Indirect Inhibition of Transmembrane Protease, Serine 2 (TMPRSS2)
    Official Title
    Efficacy of Aerosol Combination Therapy of 13 Cis Retinoic Acid and Captopril for Treating Covid-19 Patients Via Indirect Inhibition of Transmembrane Protease, Serine 2 (TMPRSS2)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2020
    Overall Recruitment Status
    Unknown status
    Study Start Date
    November 2020 (Anticipated)
    Primary Completion Date
    December 2020 (Anticipated)
    Study Completion Date
    January 2021 (Anticipated)

    3. Sponsor/Collaborators

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

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Efficacy of Aerosol Combination Therapy of 13 Cis Retinoic Acid and Captopril for Treating Covid-19 Patients Via Indirect Inhibition of Transmembrane Protease, Serine 2 (TMPRSS2) Severe acute respiratory syndrome coronavirus 2 (SARS-COV-2) has infected over 20,000,000 people causing over 700,000 deaths. It has no currently approved treatments.Airborne SARS-CoV-2 infections in humans initiate from the virus entering nasal and airway epithelial cells through binding to angiotensin-converting enzyme 2 (ACE2). Transmembrane protease, serine 2 (TMPRSS2), a cellular protease that activates the SARS-CoV-2 spike protein, colocalizes with ACE2 and can prime SARS-CoV-2 fusion directly at the plasma membrane. Transmembrane protease, serine 2 (TMPRSS2) is an androgen receptor signaling target gene and an androgen-regulated cell-surface serine protease expressed predominantly in prostate and lung epithelial cell. TMPRSS2 is normally expressed several folds higher in the prostate relative to any other human tissue, though the normal physiological function(s) remains unknown. A study found that dihydrotestosterone (DHT) s a potent activator of TMPRSS2.On the other hand, Feily et al noted that low-dose isotretinoin (0.5 mg/kg/day for 15-20 weeks) in PCO patients with moderate to severe nodulocystic acne resulted in significant decreases in levels of serum total testosterone, prolactin, and dihydrotestosterone A study demonstrated that 13- cis -Retinoic acid competitively and reversibly inhibits dihydrotestosterone. Therefore, we suggest that 13- cis -Retinoic acid will downregulate TMPRSS2 expression thorough temporary preventing the effect of dihydrotestosterone (DHT) on the activation of TMPRSS2 gene expression. ACE inhibitors and ARBs are commonly taken by heart patients to reduce blood pressure and to treat heart failure.Earlier studies had cautioned that this class of drugs could possibly increase the risk for the novel coronavirus, SARS-CoV-2, infection and elevate COVID-19 severity. There is conflicting observational evidence about the potential clinical impact of ACE inhibitors and ARBs on patients with COVID-19. Select preclinical investigations have raised concerns about their safety in patients with COVID-19. On the other hand, Preliminary data hypothesise that angiotensin-converting enzyme (ACE) inhibitors and renin-angiotensin- aldosterone system (RAAS) inhibitors could benefit patients with COVID-19 by decreasing acute lung damage and preventing angiotensin-II-mediated pulmonary inflammation. Here in our review, we use established and emerging evidence based on the findings of previous studies and researches to propose that ACE inhibitors may benefit patients with COVID-19 via attenuating and abolishing the effect of androgenic hormones on inducing the expression of Transmembrane protease, serine 2 (TMPRSS2), even though, at the same time, ACE inhibitors cause an increase in the human cell surface receptor protein ACE2 which the novel coronavirus uses to enter and infect cells. A study on hypertensive rats demonstrated that using ACE inhibitors(captopril) abolished and attenuated the effect of dihydrotestosterone (DHT). In this study RAS inhibition exhibited beneficial effects on androgen-induced obesity and abolished the androgen-mediated increase in blood pressure (BP) observed in this model of PCOS. (83 ± 1 vs 115 ± 3 mmHg, p<0.0001). A another study found that the angiotensin converting enzyme inhibitor captopril abolished testosterone effect and attenuates testosterone-induced benign prostatic hyperplasia in rats; a mechanistic approach. Captopril is a potent inhibitor of the angiotensin converting enzyme. These effects of testosterone were almost prevented by captopril (100 mg/kg). In conclusion, generally treatment with ACE inhibitors is associated with reduced androgen levels. Therefore,we think that Transmembrane protease, serine 2 (TMPRSS2) is an indirect target of ACE inhibitors and 13 cis retinoic acid As aresult, we hypothesize that any drug which downregulates TMPRSS2 expression through targeting AR, AR co-regulatory factors, or AR downstream transcription factors might be potentially effective against COVID-19 and is worth investigating under a clinical trial.. Keywords: COVID -19, Transmembrane protease, serine 2 (TMPRSS2), ACE inhibitors, ACE2.
    Detailed Description
    This is a Phase 2, , randomized (1:1:1), placebo-controlled, 2-weeks, proof-of-concept study to evaluate the safety and tolerability as well as the mechanistic effect of Aerosol administration of Aerosolized 13 cis retinoic acid plus Inhalation administration by nebulization captopril 25mg in subjects infected with COVID -19 After randomization and standard treatment The infected patients will receive Aerosolized 13 cis retinoic acid plus Inhalation administration by nebulization captopril 25mg once daily. for 14 days Outcome Measures Primary Outcome Measure lung injury score Proportion of lung injury score decreased or increased after treatmen [Time Frame: at 7and 14 days] Secondary Outcome Measures: Transe membrane protease ,serine II (TMPRSS2) changes over time [Time Frame: at day 7 and 14] Testosterone levels changes over time [Time Frame: at day 7 and 14] Dihydrotestosterone(DHT) levels changes over time [Time Frame: at day 7 and 14]] Cholesterol levels changes over time [Time Frame: at day 7 and 14] Angiotensin 1-7 (Ang 1-7) changes over time [Time Frame: at day 7 and 14] Angiotensin 1-5 (Ang 1-5) changes over time [Time Frame: at day 7 and 14] Renin changes over time [Time Frame: at day 7 and 14] Aldosterone changes over time [Time Frame: at day 7 and 14] Angiotensin-converting enzyme (ACE) changes over time [Time Frame: at day 7 and 14] Time to first negative SARS-CoV-2 PCR in NP swap [Time Frame: day 7 and 14] All cause mortality rate [Time Frame: day 7 and 14] Ventilation free days [Time Frame: day 7 and 14] ICU free days [Time Frame: day 7 and 14]

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Covid19

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    360 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Aerosolized 13 cis retinoic acid plus Inhalation administration by nebulization captopril 25mg
    Arm Type
    Experimental
    Arm Description
    Infected patients will receive aerosolized 13 cis retinoic acid in gradual one dose per day increases from 0.2 mg/kg/day to 4 mg/kg/day as inhaled 13 cis retinoic acid therapy for 14 days plus Inhalation administration by nebulization captopril 25mg for 14 days
    Arm Title
    The standard therapy
    Arm Type
    Sham Comparator
    Arm Description
    infected patients will receive the standard therapy for COVID-19 for 14 days
    Intervention Type
    Combination Product
    Intervention Name(s)
    Aerosolized 13 cis retinoic acid plus Inhalation administration by nebulization captopril 25mg
    Intervention Description
    Infected patients will receive aerosolized 13 cis retinoic acid in gradual one dose per day increases from 0.2 mg/kg/day to 4 mg/kg/day as inhaled 13 cis retinoic acid therapy for 14 days plus Inhalation administration by nebulization captopril 25mg for 14 days
    Intervention Type
    Drug
    Intervention Name(s)
    Drug: Standard treatment Standard treatment
    Intervention Description
    Drug: Standard treatment Standard treatment is according to the protocol of treatment of 2019-nCoV infection
    Primary Outcome Measure Information:
    Title
    lung injury score
    Description
    Proportion of lung injury score decreased or increased after treatmen
    Time Frame
    at 7days
    Secondary Outcome Measure Information:
    Title
    Transe membrane protease ,serine II (TMPRSS2) changes over time
    Time Frame
    at day 7 and 14
    Title
    Testosterone levels changes over time
    Time Frame
    at day 7 and 14
    Title
    Dihydrotestosterone(DHT) levels changes over time
    Time Frame
    at day 7 and 14]
    Title
    Cholesterol levels changes over time
    Time Frame
    at day 7 and 14
    Title
    Angiotensin 1-7 (Ang 1-7) changes over time
    Time Frame
    at day 7 and 14
    Title
    Angiotensin 1-5 (Ang 1-5) changes over time
    Time Frame
    at day 7 and 14
    Title
    Renin changes over time
    Time Frame
    at day 7 and 14
    Title
    Aldosterone changes over time
    Time Frame
    at day 7 and 14
    Title
    Angiotensin-converting enzyme (ACE) changes over time
    Time Frame
    at day 7 and 14
    Title
    Time to first negative SARS-CoV-2 PCR in NP swap
    Time Frame
    day 7 and 14
    Title
    All cause mortality rate
    Time Frame
    day 7 and 14
    Title
    Ventilation free days
    Time Frame
    day 7 and 14
    Title
    ICU free days
    Time Frame
    day 7 and 14

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Adult SARI patients with 2019-ncov infection confirmed by PCR; Absolute value of lymphocytes < 0. 6x 109/L; Severe respiratory failure within 48 hours and requires admission to ICU. (severe respiratory failure was defined as PaO2/FiO2 < 200 mmHg and was supported by positive pressure mechanical ventilation (including non-invasive and invasive mechanical ventilation, PEEP>=5cmH2O)) Exclusion Criteria: Age < 18 Pregnant Allergic to experimental drugs and patients have the following conditions: Hypercholesterolemia Hypertriglyceridemia Liver disease Renal disease Sjögren syndrome Pregnancy Lactation Depressive disorder Body mass index less than 18 points or higher than 25 points Contraindications for hormonal contraception or intrauterine device. Autoimmune diseases A history of organ, bone marrow or hematopoietic stem cell transplantation Patients receiving anti-hcv treatment Permanent blindness in one eye History of iritis, endophthalmitis, scleral inflammation or retinitis 15-90 days of retinal detachment or eye surgery History of ACE-inhibitor allergy History of angio-oedema Co-infection with another respiratory pathogen which could be responsible of pneumonia Hypersensitivity to captopril, to any other angiotensin converting enzyme inhibitor or any of the excipients of the specialty used Shock requiring vasopressor infusion Patient on state medical ai The competent physician considered it inappropriate to participate in the study
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Mahmoud Elkazzaz, B.Sc in Biochemistry
    Phone
    00201090302015
    Email
    mahmoudramadan2051@yahoo.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mahmoud Elkazzaz, B.Sc in Biochemistry
    Organizational Affiliation
    Faculty of Science, Damietta University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Efficacy of Aerosol Combination Therapy of 13 Cis Retinoic Acid and Captopril for Treating Covid-19 Patients Via Indirect Inhibition of Transmembrane Protease, Serine 2 (TMPRSS2)

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