Mesenchymal Stromal Cells for COVID-19 and Viral Pneumonias (SAMPSON-1)

Medical University of South Carolina (MUSC)

Status and phase

Withdrawn

Phase 1

Conditions

COVID-19 Pneumonia

Viral Pneumonia

Treatments

Biological: Allogeneic Mesenchymal Stromal Cells

Study type

Interventional

Funder types

Other

Identifiers

NCT05286255

115966

Details and patient eligibility

About

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.

Full 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:

Rapid deterioration of respiratory or clinical status within 6 hours after transfusion of UC-MSCs

Secondary Safety Endpoints:

Cumulative incidence of serious adverse events during the study period
Transfer to intensive care unit (ICU)
Type and duration of respiratory support (and other ICU support)
ICU mortality and length of stay
Hospital mortality and length of stay
Ventilator-free days
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.

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Hospitalized with COVID-19 respiratory symptoms and confirmation via COVID-19 SARS-CoV-2 RT-PCR testing.
Patient or their surrogate is willing and able to provide written informed consent and comply with all protocol requirements.
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
Patient agrees to storage of specimens for future testing.
Willingness to undergo mechanical ventilation for worsening

Exclusion criteria

Intubation with mechanical ventilation prior to study enrolment. High flow nasal cannula and non-invasive mechanical ventilation is allowed.
Pneumonia caused by bacteria, mycoplasma, chlamydia, legionella, fungi or other viruses
Obstructive pneumonia induced by lung cancer or other known causes
Significant comorbid illness likely to impact the outcome of COVID-19 including but not limited to active malignancy other than skin cancer.
Patients who are participating in other therapeutic clinical trials within 30 days of consent.
History of long-term use of immunosuppressive agents including prednisone dose >5mg daily over the 30 days prior to enrollment.
History of severe chronic respiratory disease and requirement for long-term oxygen therapy
Undergoing hemodialysis or peritoneal dialysis
Estimated or actual rate of creatinine clearance < 15 ml/min
History of moderate and severe liver disease (Child-Pugh score >12)
Substance abuse sufficient that the patient is unlikely to comply with testing requirements.
History of deep venous thrombosis, pulmonary embolism, cerebral vascular disease within the last 3 years
Known HIV, hepatitis virus, or syphilis infection
Co-Infection of tuberculosis, influenza virus, adenovirus and other respiratory infection virus
Moribund patient not expected to survive > 24hours
Allergy to diphenhydramine, or hydrocortisone
Any condition unsuitable for the study as determined by the investigators
Female subjects with positive pregnancy test, breastfeeding, or planning to become pregnant/breastfeed during the study period.
Receipt of experimental therapy for COVID-19 with the exception of convalescent plasma, dexamethasone or another corticosteroid, or remdesivir in an open label study.