COVID-19 Pneumonia, Viral Pneumonia
Conditions
Keywords
Mesenchymal Stromal Cells, ARDS, COVID-19, MSC, Stem Cells
Brief summary
This is an open-label phase 1 clinical trial of allogeneic umbilical cord derived mesenchymal stromal cells (MSCs) for hospitalized individuals with COVID-19 or other viral pneumonias. Hospitalized individuals who are within 7 days of the onset of a viral pneumonia will be given 2 doses of MSCs at days 1 and 3 after consent. The safety of intravenous infusion will be tested and course of the oxygen response to treatment over 90 days will be evaluated.
Detailed description
Study Design: This open-label phase 1 trial in 10 patients will assess the efficacy and safety of UC-MSCs given on day 1 and 3 in hospitalized patients with acute respiratory symptoms between 1 and 7 days after the onset of symptoms. The following will be assessed in all subjects: * Age, sex, comorbidities, date of symptoms, source of infection, type of admission, APACHE II score, SOFA score, Clinical status, vital signs including temperature, respiratory rate, oxygen saturation, oxygen requirement, CBC with neutrophil counts, lymphocyte count, CRP, chest imaging (CT or X-ray), location and status in hospital. * Safety and efficacy: Day 0 (baseline), 3, and 5. Monitoring at 14, 21 and 28 days and monthly for 3 months will be obtained by telephone consult and chart review with serial laboratory. * Serum or plasma antibody titer to SARS-CoV-2: Day 0, and 5 (additional days 14, 21 and 28 may be included, as available). * SARS-CoV-2 PCR from nasopharyngeal swabs: Day 0 and 5. (additional day 14, 28 and 60 day samples may be tested if available or at any time when there is clinical suspicion for COVID-19 persistence). * Outcome measures: O2 requirement (PaO2/FiO2 ratio or SpO2/FIo2), supplemental oxygen strategy (nasal cannula, high flow nasal cannula, noninvasive ventilation, intubation and invasive mechanical ventilation, neuromuscular blocking agent use, prone positioning, corticosteroids, ECMO), vasopressors, renal support, ICU LOS, ICU mortality, Hospital LOS, Hospital mortality, 28 day mortality. Study Agent: • Allogeneic UC-MSCs given intravenously at 1.2-1.5 x 106 cells/kg on day 1 and day 3 of study entry. A maximum dose of 100 x 106 cells would be given in each dose. All cellular product will be given with actively growing cells \>24 hours from the time of thawing in the Center for Cellular Therapy (CCT) at MUSC. Any emerging FDA guidance will be followed. Primary Safety Objective: Evaluate the safety of treatment with UC-MSCs in hospitalized patients with COVID-19 and respiratory symptoms. Primary Safety Endpoint: 1\. Rapid deterioration of respiratory or clinical status within 6 hours after transfusion of UC-MSCs Secondary Safety Endpoints: 1. Cumulative incidence of serious adverse events during the study period 2. Transfer to intensive care unit (ICU) 3. Type and duration of respiratory support (and other ICU support) 4. ICU mortality and length of stay 5. Hospital mortality and length of stay 6. Ventilator-free days 7. 28 day mortality Exploratory Efficacy Objective: Evaluate changes in oxygenation, progression, and regression of viral pneumonias Efficacy Endpoint: Change from baseline in PaO2/FiO2 ratio at day 5 Biologic Samples will be serially collected to determine mechanisms of effect. Propensity matching of the cohort to the MUSC COVID-19 Biorepository population will provide a population for comparison.
Interventions
BIOLOGICALAllogeneic Mesenchymal Stromal Cells
Intravenous MSCs 1.2-1.5 x 10\^6 cells/kg on Days 1 and 3 after study enrollment
Sponsors
Pandorum International, Inc.
Medical University of South Carolina
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Open label, single group, Phase 1 study
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Hospitalized with COVID-19 respiratory symptoms and confirmation via COVID-19 SARS-CoV-2 RT-PCR testing. 2. Patient or their surrogate is willing and able to provide written informed consent and comply with all protocol requirements. 3. Diagnosis with Mild or Moderate Pneumonia not requiring mechanical ventilation: Patient must have at least one of the following features: i. Bilateral pneumonia present on chest radiograph or computed tomography ii. Partial pressure of oxygen/fraction of inspired oxygen (PaO2/FiO2) on arterial blood gas showing: \>100mmHg and ≤ 300mmHg regardless of oxygen dose at time of testing. iii. Pulse oxygen saturation (SpO2) at rest ≤ 93% or any degree of hypoxia requiring supplemental oxygen 4. Patient agrees to storage of specimens for future testing. 5. Willingness to undergo mechanical ventilation for worsening
Exclusion criteria
1. Intubation with mechanical ventilation prior to study enrolment. High flow nasal cannula and non-invasive mechanical ventilation is allowed. 2. Pneumonia caused by bacteria, mycoplasma, chlamydia, legionella, fungi or other viruses 3. Obstructive pneumonia induced by lung cancer or other known causes 4. Significant comorbid illness likely to impact the outcome of COVID-19 including but not limited to active malignancy other than skin cancer. 5. Patients who are participating in other therapeutic clinical trials within 30 days of consent. 6. History of long-term use of immunosuppressive agents including prednisone dose \>5mg daily over the 30 days prior to enrollment. 7. History of severe chronic respiratory disease and requirement for long-term oxygen therapy 8. Undergoing hemodialysis or peritoneal dialysis 9. Estimated or actual rate of creatinine clearance \< 15 ml/min 10. History of moderate and severe liver disease (Child-Pugh score \>12) 11. Substance abuse sufficient that the patient is unlikely to comply with testing requirements. 12. History of deep venous thrombosis, pulmonary embolism, cerebral vascular disease within the last 3 years 13. Known HIV, hepatitis virus, or syphilis infection 14. Co-Infection of tuberculosis, influenza virus, adenovirus and other respiratory infection virus 15. Moribund patient not expected to survive \> 24hours 16. Allergy to diphenhydramine, or hydrocortisone 17. Any condition unsuitable for the study as determined by the investigators 18. Female subjects with positive pregnancy test, breastfeeding, or planning to become pregnant/breastfeed during the study period. 19. Receipt of experimental therapy for COVID-19 with the exception of convalescent plasma, dexamethasone or another corticosteroid, or remdesivir in an open label study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical deterioration | 6 hours | Change in oxygen saturation or clinical symptoms |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Respiratory support | 90 days | Type and duration of respiratory support |
| Hospital mortality and length of stay | 90 days | Hospital mortality and length of stay |
| Ventilator free days | 90 Days | Days off of mechanical ventilation |
| 28 day mortality | 28 days | 28 day mortality |
| Serious Adverse Events | 90 days | Cumulative incidence of all serious adverse events |
| ICU transfer | 90 days | Need for transfer to an intensive care unit |
Other
| Measure | Time frame | Description |
|---|---|---|
| Nasopharyngeal swab SARS-CoV-2 RT-PCR | Day 5 | Rates, levels and duration of SARS-CoV-2 RNA in nasopharyngeal swabs using RT-PCR |
| Change is PaO2/FiO2 ratio from baseline to day 5 | 5 days | Change in oxygenation |
| Anti-SARS-CoV-2 titers | 14, 21 and 28 days | Antibody titers to the SARS-CoV-2 virus |
Countries
United States
Outcome results
None listed