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Efficacy of Captopril in Covid-19 Patients With Severe Acute Respiratory Syndrome (SARS) CoV-2 Pneumonia (CAPTOCOVID) (CAPTOCOVID)

Primary Purpose

Pneumonia, Coronavirus Infection, COVID-19

Status
Unknown status
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
captopril 25mg
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pneumonia

Eligibility Criteria

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

Inclusion Criteria:

  1. Hospitalization for acute respiratory failure requiring oxygen administration ≥3L/mn
  2. Age > 18 years or older
  3. Presence of pneumonia
  4. PCR SARS-CoV-2 positive in any biological sample in the last 7 days
  5. Patient affiliated to social security regime
  6. Written informed consent provided by the patient or alternatively by next-of-kin, or in emergency situations, prior to any protocol-specific procedures

Exclusion Criteria:

  1. Decision of withholding invasive mechanical ventilation
  2. Shock requiring vasopressor infusion
  3. Co-infection with another respiratory pathogen which could be responsible of pneumonia
  4. Hypersensitivity to captopril, to any other angiotensin converting enzyme inhibitor or any of the excipients of the specialty used
  5. History of angio-oedema
  6. History of ACE-inhibitor allergy
  7. Known pregnancy or current lactation: Female subject of childbearing potential should have a negative serum pregnancy test prior to receiving the first dose of study medication.
  8. Patient who is currently enrolled in other investigational study;
  9. Persons deprived of their liberty by judicial or administrative decision,
  10. Persons under legal protection/safeguard of justice,
  11. Patients under duress psychiatric care,
  12. Persons admitted to a health or social institution
  13. Patient on state medical aid

Sites / Locations

  • CH Victor Dupuy- Argenteuil
  • Hôpital Avicenne,
  • Hôpital Avicenne
  • Hôpital Avicenne
  • Hôpital Antoine Béclère
  • CH de Compiègne-Noyon
  • Groupe hospitalier Sud Ile de France
  • Hôpital de la Pitié- Salpêtrière
  • Hôpital Tenon
  • CHRU de Tours, Hôpital Bretonneau
  • Hôpital de Tours

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

CAPTOPROL

STANDARS CARE

Arm Description

Inhalation administration by nebulization

According to surviving covid-Campaign guidelines

Outcomes

Primary Outcome Measures

Efficacy of captopril nebulization addition to standard of care compared to standard of care.
To assess determine the efficacy of captopril nebulization addition to standard of care compared to standard of care in term of 14-day ventilation free survival

Secondary Outcome Measures

Full Information

First Posted
April 17, 2020
Last Updated
April 24, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT04355429
Brief Title
Efficacy of Captopril in Covid-19 Patients With Severe Acute Respiratory Syndrome (SARS) CoV-2 Pneumonia (CAPTOCOVID)
Acronym
CAPTOCOVID
Official Title
Efficacy of Captopril Nebulization in Covid-19 Patients Suffering of SARS CoV-2 Pneumonia. A Randomized Phase II Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 5, 2020 (Anticipated)
Primary Completion Date
July 2020 (Anticipated)
Study Completion Date
August 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

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
Captopril being an effective drug available in liquid preparation, administration by nebulization could be of interest for maximizing lung action and minimizing systemic side effects. Such a treatment might be used for "Covid-19" patients with pneumonia in order to avoid ARDS.
Detailed Description
Coronavirus Disease 2019 (COVID-19) is due to SARS-CoV-2 infection. The main cause of death is refractory acute respiratory distress syndrome (ARDS) secondary to SARS-CoV-2 pneumonia. The SARS-CoV-2 may have specific virulence factors to achieve mortality rates around 3%. As the SARS-CoV, virus responsible of the Severe Acute Respiratory Syndrome in 2003 (which mortality was around 10%), the SARS-CoV-2 uses angiotensin-converting enzyme 2 (ACE2) as the receptor binding domain for its spike protein making ACE2 the gateway in the alveolar epithelial cells1. Angiotensin-converting enzyme (ACE) and ACE2 are known to be present in respiratory epithelium and to have antagonist physiological functions. ACE2 has an anti-inflammatory, anti-fibrosing role, anti-oxydant and vasodilatator activity, while ACE has the opposite characteristics. These two enzymes have a negative control on each other, one inhibiting the other. Demonstrated that SARS-CoV is responsible of a downregulation of ACE2 functions by using ACE2 as cell receptor2. While ACE2 is downregulated, ACE activity increase leading to more alveolar damage and acute respiratory failure. ACE inhibitors are common drugs used to treat hypertension worldwide. Using an ACE inhibitor as treatment against SARS-CoV-2 could be counter-intuitive because increasing ACE2 expression would open the cellular gate to the virus3,4. However, ACE2 was described as protecting lung injury2, leading Recombinant Human ACE2 as a perspective for SARS-CoV-2 treatment. A simple way to increase ACE2 in patients with SARS-CoV-2 pneumonia could be an inhalation of ACE inhibitor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pneumonia, Coronavirus Infection, COVID-19

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
CAPTOPROL
Arm Type
Experimental
Arm Description
Inhalation administration by nebulization
Arm Title
STANDARS CARE
Arm Type
No Intervention
Arm Description
According to surviving covid-Campaign guidelines
Intervention Type
Drug
Intervention Name(s)
captopril 25mg
Other Intervention Name(s)
Any
Intervention Description
Drug administration
Primary Outcome Measure Information:
Title
Efficacy of captopril nebulization addition to standard of care compared to standard of care.
Description
To assess determine the efficacy of captopril nebulization addition to standard of care compared to standard of care in term of 14-day ventilation free survival
Time Frame
14 Days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hospitalization for acute respiratory failure requiring oxygen administration ≥3L/mn Age > 18 years or older Presence of pneumonia PCR SARS-CoV-2 positive in any biological sample in the last 7 days Patient affiliated to social security regime Written informed consent provided by the patient or alternatively by next-of-kin, or in emergency situations, prior to any protocol-specific procedures Exclusion Criteria: Decision of withholding invasive mechanical ventilation Shock requiring vasopressor infusion 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 History of angio-oedema History of ACE-inhibitor allergy Known pregnancy or current lactation: Female subject of childbearing potential should have a negative serum pregnancy test prior to receiving the first dose of study medication. Patient who is currently enrolled in other investigational study; Persons deprived of their liberty by judicial or administrative decision, Persons under legal protection/safeguard of justice, Patients under duress psychiatric care, Persons admitted to a health or social institution Patient on state medical aid
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohammed RAHAOUI, PM
Phone
+33 1 48 95 59 77
Email
mohammed.rahaoui@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Yacine TANDJAOUI-LAMBIOTTE, MD
Email
yacine.tandjaoui-lambiotte@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yacine TANDJAOUI-LAMBIOTTE, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
CH Victor Dupuy- Argenteuil
City
Argenteuil
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pascale LONGUET, MD
Facility Name
Hôpital Avicenne,
City
Bobigny
ZIP/Postal Code
93000
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Olivier BOUCHAUD, Pr
Facility Name
Hôpital Avicenne
City
Bobigny
ZIP/Postal Code
93000
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yacine TANDJAOUI-LAMBIOTTE, MD
Email
yacine.tandjaoui-lambiotte@aphp.fr
Facility Name
Hôpital Avicenne
City
Bobigny
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nunes HILARIO, MD
Facility Name
Hôpital Antoine Béclère
City
Clamart
Country
France
Facility Name
CH de Compiègne-Noyon
City
Compiègne
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne-Lise LECAPITAINE, MD
Facility Name
Groupe hospitalier Sud Ile de France
City
Melun
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sylvain DIAMANTIS, MD
Facility Name
Hôpital de la Pitié- Salpêtrière
City
Paris
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alexandre BLEIBTREU, MD
Facility Name
Hôpital Tenon
City
Paris
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gilles PIALOUX, Pr
Facility Name
CHRU de Tours, Hôpital Bretonneau
City
Tours
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Louis BERNARD, MD
Facility Name
Hôpital de Tours
City
Tours
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurent PLANTIER, Pr

12. IPD Sharing Statement

Citations:
PubMed Identifier
32129518
Citation
Gurwitz D. Angiotensin receptor blockers as tentative SARS-CoV-2 therapeutics. Drug Dev Res. 2020 Aug;81(5):537-540. doi: 10.1002/ddr.21656. Epub 2020 Mar 4.
Results Reference
background
PubMed Identifier
32109013
Citation
Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, Liu L, Shan H, Lei CL, Hui DSC, Du B, Li LJ, Zeng G, Yuen KY, Chen RC, Tang CL, Wang T, Chen PY, Xiang J, Li SY, Wang JL, Liang ZJ, Peng YX, Wei L, Liu Y, Hu YH, Peng P, Wang JM, Liu JY, Chen Z, Li G, Zheng ZJ, Qiu SQ, Luo J, Ye CJ, Zhu SY, Zhong NS; China Medical Treatment Expert Group for Covid-19. Clinical Characteristics of Coronavirus Disease 2019 in China. N Engl J Med. 2020 Apr 30;382(18):1708-1720. doi: 10.1056/NEJMoa2002032. Epub 2020 Feb 28.
Results Reference
result
PubMed Identifier
16166518
Citation
Li F, Li W, Farzan M, Harrison SC. Structure of SARS coronavirus spike receptor-binding domain complexed with receptor. Science. 2005 Sep 16;309(5742):1864-8. doi: 10.1126/science.1116480.
Results Reference
result
PubMed Identifier
16001071
Citation
Imai Y, Kuba K, Rao S, Huan Y, Guo F, Guan B, Yang P, Sarao R, Wada T, Leong-Poi H, Crackower MA, Fukamizu A, Hui CC, Hein L, Uhlig S, Slutsky AS, Jiang C, Penninger JM. Angiotensin-converting enzyme 2 protects from severe acute lung failure. Nature. 2005 Jul 7;436(7047):112-6. doi: 10.1038/nature03712.
Results Reference
result
PubMed Identifier
32125455
Citation
Zhang H, Penninger JM, Li Y, Zhong N, Slutsky AS. Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target. Intensive Care Med. 2020 Apr;46(4):586-590. doi: 10.1007/s00134-020-05985-9. Epub 2020 Mar 3. No abstract available.
Results Reference
result

Learn more about this trial

Efficacy of Captopril in Covid-19 Patients With Severe Acute Respiratory Syndrome (SARS) CoV-2 Pneumonia (CAPTOCOVID)

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