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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
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 focused on measuring Mesenchymal Stromal Cells, COVID-19, Sars-CoV2

Eligibility Criteria

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

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

    First Posted
    July 7, 2020
    Last Updated
    July 9, 2020
    Sponsor
    Hospital de Clinicas de Porto Alegre
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    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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