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Umbilical Mesenchymal Stromal Cells as Cellular Immunotherapy for Septic Shock

Recruiting
18 years of age
Both
Phase 2

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Overview

Septic shock is associated with substantial burden in terms of both mortality and morbidity for survivors of this illness. Pre-clinical sepsis studies suggest that mesenchymal stem (stromal) cells (MSCs) modulate inflammation, enhance pathogen clearance and tissue repair and reduce death. Our team has completed a Phase I dose escalation and safety clinical trial that evaluated MSCs in patients with septic shock. The Cellular Immunotherapy for Septic Shock Phase I (CISS) trial established that MSCs appear safe and that a randomized controlled trial (RCT) is feasible. Based on these data, the investigators have planned a phase II RCT (UC-CISS II) at several Canadian academic centres which will evaluate intermediate measures of clinical efficacy (primary outcome), as well as biomarkers, safety, clinical outcome measures, and a health economic analysis (secondary outcomes).

Description

Septic shock is a devastating illness and the most severe form of infection seen in the intensive care unit (ICU). It is characterized by cardiovascular collapse, failure of organs and is common with severe repercussions including a mortality of 20-40%. Survivors suffer long-term impairment in function and reduced quality of life (QOL). Despite decades of research examining different immune therapies, none has proven successful and supportive care remains the mainstay of therapy, at a cost of approximately 4-billion dollars in Canada annually. MSCs represent a potentially novel treatment for sepsis because in animal models, MSCs have been shown to modulate the immune system, increase pathogen clearance, restore organ function, and reduce death.

The Phase II multi-centre double blind Umbilical Cord Cellular Immunotherapy for Septic Shock RCT (UC-CISS II) will examine intermediate measures of clinical efficacy (primary outcome) as well as biomarkers, safety, clinical outcome measures, and a health economic analysis (secondary outcomes). To answer these aims, UC-CISS II will randomize 296 patients who are admitted to the ICU with septic shock to 300 million cryopreserved, allogeneic, umbilical cord-derived MSCs or placebo across several Canadian academic centres over approximately 2.5 years.

Eligibility

Inclusion Criteria:

A participant must meet all the following inclusion criteria to be eligible:

  1. At least 18 years of age AND
  2. Requirement for admission to the intensive care unit AND
  3. Index admission to the intensive care unit AND
  4. Cardiovascular organ failure for at least 1 consecutive hour defined by the requirement of at least 5 mcg/min of norepinephrine or 100 mcg/min of phenylephrine or 0.03 U/min vasopressin AND
  5. Clinician impression that cardiovascular organ failure is related to infection AND
  6. There is at least 1 other acute organ failure according to modified individual Sequential Organ Failure Assessment Scores within 24 hours of meeting Cardiovascular organ failure defined by:
    1. Respiratory failure: invasive or non-invasive mechanical ventilation with a positive end expiratory pressure (PEEP) >/= 5 cm H2O, OR high-flow nasal canula oxygen therapy (minimum total flow rate of 40 lpm); and a partial pressure of oxygen/fractional inspired oxygen concentration (P/F ratio) </= 200 OR
    2. Hematological failure: platelet count of </= 100 X 10^9/L OR
    3. Acute kidney injury: acute renal insufficiency with a creatinine of >/= 200 umol/L, or the requirement for new renal replacement therapy, or for participants with known chronic renal failure but not on dialysis, a 50% increase in their baseline creatinine concentration OR
    4. Organ hypoperfusion: a lactate >/= 4 mmol/L
        Acute organ failures that meet eligibility criteria must not have been present for greater
        than 48 hours prior to admission to the ICU.
        Exclusion Criteria:
        Patients will be excluded if they have at least one of the following:
          1. Another form of shock (cardiogenic, hypovolemic, obstructive) OR
          2. History of known chronic pulmonary hypertension with a WHO functional class of IV OR
          3. History of severe chronic pulmonary disease requiring home oxygen OR
          4. History of severe chronic cardiac disease including congestive heart failure or
             valvular dysfunction with a New York Heart Association Functional class IV or severe
             chronic ischemic heart disease with a Canadian Cardiovascular Society angina class
             score IV OR
          5. History of severe chronic liver disease (Child-Pugh Class C or model for end stage
             liver disease (MELD) Score >= 15) OR
          6. Malignancy in previous 1 year (excluding resolved non-melanoma skin cancer) OR
          7. Treating physician impression that death is imminent within the 12 hours after meeting
             eligibility criteria OR
          8. Pregnant or lactating OR
          9. Family or patient not committed to aggressive care

Study details

Septic Shock, Sepsis, Pathologic Processes, Shock, Systemic Inflammatory Response Syndrome

NCT05969275

Ottawa Hospital Research Institute

21 February 2024

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