Safety and Feasibility of Allogenic MSC in the Treatment of COVID-19 (COVID19)
Primary Purpose
COVID-19, Sars-CoV2
Status
Unknown status
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Mesenchymal Stromal Cells infusion
Sponsored by

About this trial
This is an interventional treatment trial for COVID-19 focused on measuring Mesenchymal Stromal Cells, COVID-19, Sars-CoV2
Eligibility Criteria
Inclusion Criteria:
- Laboratory confirmation of COVID19 infection by reverse-transcription polymerase chain reaction (RT-PCR)
- The patient or legal donor agrees to participate in the study and signs the informed consent.
- Patients with orange or red criteria according to the score proposed by Liao et al (2020)
Exclusion Criteria:
- Patient with pregnancy, are planning to become pregnant or breastfeeding
- Patients with malignant blood-borne diseases such as HIV or syphilis
- Not consenting for clinical trial
- Patients with other than orange or red criteria according to the score proposed by Liao et al (2020)
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Intervention
Arm Description
Intravenous 1*10E6 MSCs/kg body weight Mesenchymal Stromal Cells infusion
Outcomes
Primary Outcome Measures
Overall survival
Assessment of Overall survival at 30 days post intervention
Secondary Outcome Measures
Changes on inflammatory C-reactive protein
To assess the anti-inflammatory effect of the proposed treatment with assessment of the levels of C-reactive protein (mg/dL)
Hospital stay
days of the patients in hospital
Oxygenation index (PaO2/FiO2)
Evaluation of functional respiratory changes: PaO2 / FiO2 ratio
Improvement in Liao's score (2020)
Improvement in Liao's score (2020)
Radiological improvement
Computed tomography Chest assesment will be done to assess improvement in radiological findings of COVID-19
Time of COVID19 PCR negativity
PCR testing to check PCR negativity
Full Information
NCT ID
NCT04467047
First Posted
July 7, 2020
Last Updated
July 9, 2020
Sponsor
Hospital de Clinicas de Porto Alegre
1. Study Identification
Unique Protocol Identification Number
NCT04467047
Brief Title
Safety and Feasibility of Allogenic MSC in the Treatment of COVID-19
Acronym
COVID19
Official Title
Safety and Feasibility of Allogenic Mesenchymal Stromal Cells in the Treatment of COVID-19
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
July 25, 2020 (Anticipated)
Primary Completion Date
October 30, 2020 (Anticipated)
Study Completion Date
December 30, 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital de Clinicas de Porto Alegre
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
Coronavirus Disease 2019 (COVID-19) is spreading worldwide and has become a public health emergency of major international concern. Currently, no specific drugs or vaccines are available. For severe cases, it was found that aberrant pathogenic T cells and inflammatory monocytes are rapidly activated and then producing a large number of cytokines and inducing an inflammatory storm. Mesenchymal stem cells (MSCs) have been shown to possess a comprehensive powerful immunomodulatory function. This study aims to investigate the safety and efficacy of intravenous infusion of mesenchymal stem cells in severe patients with COVID-19.
Detailed Description
Coronavirus-19 Disease (COVID-19), caused by the Sars-Cov-2 virus, which occurs as a growing pandemic in early 2020 and currently represents an emergency state worldwide. Several reports have shown that the first step in the pathogenesis of Sars-Cov-2 is the recognition of the angiotensin I converting enzyme (ACE2) receptor by the virus. This ACE2 receptor is widely distributed on the surface of human cells, especially as type II alveolar cells and capillary endothelium, however bone marrow, lymph nodes, thymus and spleen are known as immune cells, such as T and lymphocytes. B and macrophages, are negatives to ACE2. These results suggest that immunotherapy can be used to treat infected patients. However, an immunomodulatory capacity cannot be so strong, if just one or two major immunological factors used, as the virus can cause a "cytokine storm", such as IL-2, IL-6, IL-7, GSCF, IP10 , MCP1, MIP1A and TNFα, followed by edema, gas exchange dysfunction, acute respiratory distress syndrome, cardiac injury and secondary infection that can lead to death. Therefore, avoiding a "cytokine storm" may be the key to treating patients infected with Sars-Cov-2. Mesenchymal stem cells (MSCs), due to their potential for immunomodulatory activity, can have beneficial effects in preventing or attenuating the cytokine storm. Because MSCs have been widely used in cell therapy, from basic research to clinical trials. Safety and efficacy have been clearly documented in several clinical trials, especially in immune-mediated inflammatory diseases, such as graft versus host disease (GVHD). The objective of the study is to verify the safety and feasibility of using allogeneic bone marrow mesenchymal stem cells in patients with SARS-CoV-2.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19, Sars-CoV2
Keywords
Mesenchymal Stromal Cells, COVID-19, Sars-CoV2
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Intravenous 1*10E6 MSCs/kg body weight Mesenchymal Stromal Cells infusion
Intervention Type
Biological
Intervention Name(s)
Mesenchymal Stromal Cells infusion
Intervention Description
Intravenous 1*10E6 MSCs/kg body weight Mesenchymal Stromal Cells infusion
Primary Outcome Measure Information:
Title
Overall survival
Description
Assessment of Overall survival at 30 days post intervention
Time Frame
60 days
Secondary Outcome Measure Information:
Title
Changes on inflammatory C-reactive protein
Description
To assess the anti-inflammatory effect of the proposed treatment with assessment of the levels of C-reactive protein (mg/dL)
Time Frame
60 days
Title
Hospital stay
Description
days of the patients in hospital
Time Frame
60 days
Title
Oxygenation index (PaO2/FiO2)
Description
Evaluation of functional respiratory changes: PaO2 / FiO2 ratio
Time Frame
60 days
Title
Improvement in Liao's score (2020)
Description
Improvement in Liao's score (2020)
Time Frame
60 days
Title
Radiological improvement
Description
Computed tomography Chest assesment will be done to assess improvement in radiological findings of COVID-19
Time Frame
60 days
Title
Time of COVID19 PCR negativity
Description
PCR testing to check PCR negativity
Time Frame
28 days
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Laboratory confirmation of COVID19 infection by reverse-transcription polymerase chain reaction (RT-PCR)
The patient or legal donor agrees to participate in the study and signs the informed consent.
Patients with orange or red criteria according to the score proposed by Liao et al (2020)
Exclusion Criteria:
Patient with pregnancy, are planning to become pregnant or breastfeeding
Patients with malignant blood-borne diseases such as HIV or syphilis
Not consenting for clinical trial
Patients with other than orange or red criteria according to the score proposed by Liao et al (2020)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lucia Silla, MD, PhD
Phone
55 51 33598371
Email
lsilla@hcpa.edu.br
First Name & Middle Initial & Last Name or Official Title & Degree
Annelise Pezzi, PhD
Email
annepezzi@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lucia Silla, MD, PhD
Organizational Affiliation
Hospital de Clinicas de Porto Alegre
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Safety and Feasibility of Allogenic MSC in the Treatment of COVID-19
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