Mesenchymal Stromal Cells for COVID-19 and Viral Pneumonias

COVID-19 Pneumonia Clinical Trial

— SAMPSON-1  

Official title:

Safety and Tolerability of Allogeneic Umbilical Cord Derived Mesenchymal Stromal Cells (UC-MSCs) to Limit COVID Associated ComplicatioNs: An Open Label, Phase 1 Study in Hospitalized Patients (SAMPSON-1)

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05286255
• Other study ID #: 115966
• Status: Not yet recruiting
• Phase: Phase 1
• Start date: September 2024
• Est. completion date: May 2027

Study information

• Verified date: November 2023
• Source: Medical University of South Carolina
• Contact: Charlie Strange, MD
• Phone: 843-792-3174
• Email: strangec[@]musc.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 10
• Est. completion date: May 2027
• Est. primary completion date: December 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

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.

Related Conditions & MeSH terms

• COVID-19
• COVID-19 Pneumonia
• Pneumonia
• Pneumonia, Viral
• Viral Pneumonia

Intervention

Biological:
• Allogeneic Mesenchymal Stromal Cells
Intravenous MSCs 1.2-1.5 x 10^6 cells/kg on Days 1 and 3 after study enrollment

Locations

Country	Name	City	State
United States	Medical University of South Carolina	Charleston	South Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Medical University of South Carolina	Pandorum International, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change is PaO2/FiO2 ratio from baseline to day 5	Change in oxygenation	5 days
Other	Anti-SARS-CoV-2 titers	Antibody titers to the SARS-CoV-2 virus	14, 21 and 28 days
Other	Nasopharyngeal swab SARS-CoV-2 RT-PCR	Rates, levels and duration of SARS-CoV-2 RNA in nasopharyngeal swabs using RT-PCR	Day 5
Primary	Clinical deterioration	Change in oxygen saturation or clinical symptoms	6 hours
Secondary	Serious Adverse Events	Cumulative incidence of all serious adverse events	90 days
Secondary	ICU transfer	Need for transfer to an intensive care unit	90 days
Secondary	Respiratory support	Type and duration of respiratory support	90 days
Secondary	Hospital mortality and length of stay	Hospital mortality and length of stay	90 days
Secondary	Ventilator free days	Days off of mechanical ventilation	90 Days
Secondary	28 day mortality	28 day mortality	28 days