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Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV) (COVID_MSV)

Primary Purpose

COVID-19 Pneumonia

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
Mesenchymal Stromal Cells
Placebo
Sponsored by
Red de Terapia Celular
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 Pneumonia focused on measuring COVID-19, Mesenchymal Stromal Cells, MSV

Eligibility Criteria

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

Inclusion Criteria:

  1. Women or men of ≥ 18 years of age
  2. SARS-CoV-2 infection confirmed by molecular testing.
  3. Admitted to the Intensive Care Unit with pneumonia by COVID-19 infection in the last 48 hours, that meet at least one of these criteria:

    1. Respiratory distress.
    2. Respiratory rate (FR) ≥ 30 rpm.
    3. Basal oxygen saturation at rest ≤ 93%.
    4. Arterial partial pressure of oxygen (PaO₂) / inspiratory fraction of oxygen (FiO₂) ≤300mmHg
  4. Consent of the patient or his legal representative for participation in the study.

Exclusion Criteria:

  1. Active tumor disease.
  2. Pregnancy.
  3. Participation in another clinical trial for the same pathology.
  4. Any circumstance that in the researcher's opinion justifies the patient's non-participation in the trial.
  5. Lack of signed consent for participation.

Sites / Locations

  • Hospital Universitario Rio Hortega

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Experimental

Placebo

Arm Description

Intravenous injection of 1 million MSV cells/Kg in 100 ml of saline

Intravenous injection of 100 ml of saline containing no cells

Outcomes

Primary Outcome Measures

Proportion of patients who have achieved withdrawal of invasive mechanical ventilation
Index of therapy success to preserve Intensive Care Hospitalization space
Rate of mortality
To measure global success

Secondary Outcome Measures

Proportion of patients who have achieved clinical response
Index based in the 4 most relevant symptoms and signs: fever, shortness of bread, %Hemoglobin Saturation and PaO2 / FiO2
Proportion of patients who have achieved radiological responses
Evaluation of pneumonia changes

Full Information

First Posted
April 17, 2020
Last Updated
June 6, 2022
Sponsor
Red de Terapia Celular
Collaborators
Citospin, University of Valladolid, Castilla-León Health Service, Hospital del Río Hortega, Instituto de Salud Carlos III
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1. Study Identification

Unique Protocol Identification Number
NCT04361942
Brief Title
Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV)
Acronym
COVID_MSV
Official Title
Double Blind, Placebo-controlled, Phase II Trial to Evaluate Safety and Efficacy of Allogenic Mesenchymal Stromal Cells MSV_allo for Treatment of Acute Respiratory Failure in Patients With COVID-19 Pneumonia (COVID_MSV)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
October 28, 2021 (Actual)
Study Completion Date
October 28, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Red de Terapia Celular
Collaborators
Citospin, University of Valladolid, Castilla-León Health Service, Hospital del Río Hortega, Instituto de Salud Carlos III

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
Novel coronavirus COVID-19 has become a health emergency around the world. Since first patients were detected in Wuhan China, in December 2019, COVID-19 has spread quickly worldwide, being a severe threat to public health. Fever, dry cough, shortness of breath and breathing distress are the main characteristics of COVID-19 infection. Some patients develop overwhelming lung inflammation and acute respiratory failure, for which there is no specific therapy. Therefore, safe and effective treatment for COVID-19 pneumonia is utterly necessary, mainly in critical cases. Mesenchymal stem cells (MSCs) have been widely used in the immune-mediated inflammatory diseases. MSCs can regulate both innate and adaptive immunity by suppressing the proliferation, differentiation and activation of different cells. These immunomodulatory properties of MSCs support performance of the phase I/II, placebo- controlled, randomized MSCs for treatment of severe COVID-19 pneumonia.
Detailed Description
Novel coronavirus COVID-19 has spread quickly from Wuhan China to worldwide. On 15 April 2020, the World Health Organization (WHO) has reported 1.914.916 confirmed cases and 123.010 deaths globally, being a severe threat to public health. Some patients develop overwhelming lung inflammation and acute respiratory failure. Several reports demonstrated that COVID-19 specifically recognized the angiotensin I converting ezyme 2 repector (ACE2) and ACE2-positive cells are infected by the virus. ACE2 receptor is widely present on the human cells surface such as alveolar type II cells and capillary endothelium, among others. COVID-19 infects cells and stimulates a terrible cytokine storm in the lung followed by edema, dysfunction of the air exchange and acute respiratory distress which may lead to death. Further, once COVID-19 enters in blood circulation, it can easy spread to some systems and organs, causing significant damage. Under these circumstances, it is reasonable to believe that the inhibition of inflammatory response is the key to treat COVID-19 pneumonia. Mesenchymal stem cells (MSCs) have been widely used in the immune-mediated inflammatory diseases. MSCs can regulate both innate and adaptive immunity by suppressing the proliferation, differentiation and activation of different cells. Some studies have shown that MSCs can significantly reduce acute lung injury in mice caused by H9N2 and H5N1 virus, reducing proinflammatory cytokines and inflammatory cells into the lungs. These immunomodulatory properties of MSCs support performance of the Phase I/II, double-blind (neither the participant nor the investigator will know if active drug or placebo is assigned), placebo-controlled, randomized (assigned by chance), in which subjects with severe COVID-19 pneumonia shall be received either MSCs (1 million cells/kg) or placebo by intravenous injection. The administration of cells will be done only once.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19 Pneumonia
Keywords
COVID-19, Mesenchymal Stromal Cells, MSV

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Masking Description
Both experimental and Placebo will receive a similar endovenous injection with either cells or placebo. Blind to participant, investigator ans care providers
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental
Arm Type
Experimental
Arm Description
Intravenous injection of 1 million MSV cells/Kg in 100 ml of saline
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Intravenous injection of 100 ml of saline containing no cells
Intervention Type
Biological
Intervention Name(s)
Mesenchymal Stromal Cells
Other Intervention Name(s)
MSV
Intervention Description
Intravenous injection of 1 million MSV cells/Kg diluted in 100 ml saline
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Intravenous injection of 100 ml saline containing no cells
Primary Outcome Measure Information:
Title
Proportion of patients who have achieved withdrawal of invasive mechanical ventilation
Description
Index of therapy success to preserve Intensive Care Hospitalization space
Time Frame
0-7 days
Title
Rate of mortality
Description
To measure global success
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Proportion of patients who have achieved clinical response
Description
Index based in the 4 most relevant symptoms and signs: fever, shortness of bread, %Hemoglobin Saturation and PaO2 / FiO2
Time Frame
0-7days
Title
Proportion of patients who have achieved radiological responses
Description
Evaluation of pneumonia changes
Time Frame
0-28 days
Other Pre-specified Outcome Measures:
Title
Blood white cell counts and their subpopulations.
Description
Haemogram and cell subpopulations
Time Frame
0-180 days
Title
Cellular markers of inflammation
Description
Lymphocyte profiles, CD3, CD19, CD16+CD56, CD4/CD8, Tregs
Time Frame
0-180 days
Title
Cytokines and chemokines in peripheral blood
Description
IL-10, IL-6, IP-10, TNF-alpha
Time Frame
0-180 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women or men of ≥ 18 years of age SARS-CoV-2 infection confirmed by molecular testing. Admitted to the Intensive Care Unit with pneumonia by COVID-19 infection in the last 48 hours, that meet at least one of these criteria: Respiratory distress. Respiratory rate (FR) ≥ 30 rpm. Basal oxygen saturation at rest ≤ 93%. Arterial partial pressure of oxygen (PaO₂) / inspiratory fraction of oxygen (FiO₂) ≤300mmHg Consent of the patient or his legal representative for participation in the study. Exclusion Criteria: Active tumor disease. Pregnancy. Participation in another clinical trial for the same pathology. Any circumstance that in the researcher's opinion justifies the patient's non-participation in the trial. Lack of signed consent for participation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julia Barbado, MD, PhD
Organizational Affiliation
University Hospital Río Hortega, Valladolid, Spain
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rosa Conde, MD, PhD
Organizational Affiliation
University Hospital Río Hortega, Valladolid, Spain
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Margarita González-Vallinas, PhD
Organizational Affiliation
University of Valladolid
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Rio Hortega
City
Valladolid
ZIP/Postal Code
47012
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
25822648
Citation
Vega A, Martin-Ferrero MA, Del Canto F, Alberca M, Garcia V, Munar A, Orozco L, Soler R, Fuertes JJ, Huguet M, Sanchez A, Garcia-Sancho J. Treatment of Knee Osteoarthritis With Allogeneic Bone Marrow Mesenchymal Stem Cells: A Randomized Controlled Trial. Transplantation. 2015 Aug;99(8):1681-90. doi: 10.1097/TP.0000000000000678.
Results Reference
result
PubMed Identifier
27661661
Citation
Noriega DC, Ardura F, Hernandez-Ramajo R, Martin-Ferrero MA, Sanchez-Lite I, Toribio B, Alberca M, Garcia V, Moraleda JM, Sanchez A, Garcia-Sancho J. Intervertebral Disc Repair by Allogeneic Mesenchymal Bone Marrow Cells: A Randomized Controlled Trial. Transplantation. 2017 Aug;101(8):1945-1951. doi: 10.1097/TP.0000000000001484.
Results Reference
result
PubMed Identifier
30290717
Citation
Barbado J, Tabera S, Sanchez A, Garcia-Sancho J. Therapeutic potential of allogeneic mesenchymal stromal cells transplantation for lupus nephritis. Lupus. 2018 Nov;27(13):2161-2165. doi: 10.1177/0961203318804922. Epub 2018 Oct 5.
Results Reference
result
PubMed Identifier
32257537
Citation
Leng Z, Zhu R, Hou W, Feng Y, Yang Y, Han Q, Shan G, Meng F, Du D, Wang S, Fan J, Wang W, Deng L, Shi H, Li H, Hu Z, Zhang F, Gao J, Liu H, Li X, Zhao Y, Yin K, He X, Gao Z, Wang Y, Yang B, Jin R, Stambler I, Lim LW, Su H, Moskalev A, Cano A, Chakrabarti S, Min KJ, Ellison-Hughes G, Caruso C, Jin K, Zhao RC. Transplantation of ACE2- Mesenchymal Stem Cells Improves the Outcome of Patients with COVID-19 Pneumonia. Aging Dis. 2020 Mar 9;11(2):216-228. doi: 10.14336/AD.2020.0228. eCollection 2020 Apr.
Results Reference
result

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Treatment of Severe COVID-19 Pneumonia With Allogeneic Mesenchymal Stromal Cells (COVID_MSV)

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