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LL-37

Cathelicidin, hCAP-18, FALL-39, CAP-18

Quick Stats
Studies 2230
Trials 95
Unknown PHASE2 INTERVENTIONAL NCT03369275

Cellular Immunotherapy for Septic Shock

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

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 may 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 mesenchymal stem cells (MSCs) in patients with septic shock. The Cellular Immunotherapy for Septic Shock (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 (CISS2) at several Canadian academic centres which will evaluate safety, signals for clinical efficacy, and continue to examine potential mechanisms of action and biological effects of MSCs in septic shock.

Detailed 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 Cellular Immunotherapy for Septic Shock RCT (CISS2) will continue to evaluate safety, assess if there are signals for clinical efficacy and determine mechanisms of action and biological effects of MSCs in septic shock. To answer these aims, CISS2 will randomize 114 patients who are admitted to the ICU with septic shock to 300 million cryopreserved, allogeneic, bone marrow derived MSCs or placebo across 10 Canadian centres over approximately 2 years.

Interventions

Name: Allogeneic Bone Marrow-Derived Human Mesenchymal Stem Cells
Type: BIOLOGICAL
Description: Cryopreserved Allogeneic Bone Marrow-Derived Human Mesenchymal Stem Cells will be administered intravenously.
Name: Placebo
Type: OTHER
Description: Placebo, with excipients, will be administered intravenously.

Primary Outcomes

Measure: The reduction in days on mechanical ventilation, or renal replacement therapy, or vasopressors.
TimeFrame: Through to 28 days post-randomization
Description: The number of days free from each of these support measures.
Measure: Incidence of treatment-emergent adverse events (Safety and tolerability)
TimeFrame: Through to 28 days post-randomization
Description:

Trial Information

NCT ID

NCT03369275

Status

Unknown

Study Type

INTERVENTIONAL

Phases

PHASE2

Sponsor

Ottawa Hospital Research Institute

Last Updated

December 15, 2025