Mesenchymal Stem Cell Therapy for SARS-CoV-2-related Acute Respiratory Distress Syndrome

Covid-19 Clinical Trial

Official title:

Mesenchymal Stem Cell Therapy for Acute Respiratory Distress Syndrome in Coronavirus Infection: A Phase 2-3 Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04366063
• Other study ID #: 991919
• Secondary ID: IRCT202002170465
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: April 5, 2020
• Est. completion date: December 10, 2020

Study information

• Verified date: April 2020
• Source: Royan Institute
• Contact: Masoumeh Nouri
• Phone: 00982127635512
• Email: masoume.nouri2002[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Acute Respiratory Distress Syndrome (ARDS) is the major cause of death in the COVID-19 pandemic. In this trial, the safety and efficacy of Mesenchymal Stem Cells (MSC) for the treatment of ARDS in COVID-19 patients will be assessed.

Description:

Acute respiratory distress syndrome (ARDS) is the major cause of death in the COVID 19 infection pandemic. It is a devastating clinical condition, caused by an acute and diffuse lung injury that requires management in the intensive care unit. It is caused by uncontrolled inflammation that leads to severe pulmonary alveolar damage and capillary membrane leakage, and progressive respiratory failure. There is no effective treatment for ARDS and the only supportive care strategies are the mainstay of therapy. Mesenchymal stem cells (MSCs) have high regenerative and immunomodulatory capacities. In preclinical research, ARDS, MSCs modulate the inflammatory response, augment tissue repair, enhance pathogen clearance, and reduce the severity of the injury, pulmonary dysfunction, and apoptosis. Moreover, many studies have shown that the anti-inflammatory effects of MSCs can significantly reduce virus (e.g., Influenza)-induced lung injury and mortality in animals. Since 2014 clinical trials are using MSC from variable sources [bone marrow (BM), fat, and umbilical cord (UC)] in the treatment of ARDS. Some of the clinical trials are ongoing and the final reports are not reported. In all final reports, the safety of the application of MSC has been documented and most of them implied improvement in mortality and decrease of morbidity. Moreover, experimental studies have demonstrated that MSCs or their extracellular vesicles (MSCs-EVs) significantly reduced lung inflammation and pathological impairment resulting from different types of lung injury. Also, macrophage phagocytosis, bacterial killing, and the outcome are improved. It is highly likely that MSCs-EVs have the same therapeutic effect on inoculation pneumonia as MSCs themselves.

Critically ill coronavirus documented cases suspicious to ARDS (mild or moderate) will be enrolled in the study. Our previous experiment (IRCT20200217046526N1) showed the safety of 3 injections of MSCs in patients with COVID-19. This multi-center trial will recruit 60 patients. All patients in all groups will receive conventional therapy for virus treatment and supportive care for ARDS.

The patients allocated randomly to three groups:

Control (n=20). Patients will conventional therapy for virus treatment and supportive care for ARDS will be used as control.

Intervention Group1 (n=20). Patients will receive two doses of MSCs 100×10e6 (±10%), at Day 0 and Day 2 intravenously.

Intervention Group 2 (n=20). Patients will receive two doses of MSCs 100×10e6 (±10%), at Day 0 and Day 2 plus two doses of extracellular vesicles (EVs) on Day 4 and Day 6 intravenously.

The clinical symptoms, pulmonary imaging, side effects, 28-days mortality inflammatory factors, etc. will be evaluated during the 28 days follow up.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 10, 2020
• Est. primary completion date: June 6, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Confirmation of 2019-nCoV infection by RT-PCR

• Diagnosis of ARDS according to the Berlin definition of ARDS

• Requiring supplemental oxygen

• Pneumonia that is judged by chest radiograph or CT

• PaO2/oxygen absorption concentration (FiO2) = 300MMHG

• Pulmonary imaging shows that the focused progress > 50% in 24-48 hours

• Mild to Moderate 2019-nCoV pneumonia/ stay in the ICU <48 hours

• SOFA score between 2-3 point

Exclusion Criteria:

• Severe allergies or allergies after 1st injection to stem cell preparations and their components

• Patients with a malignant tumor, other serious systemic diseases, and psychosis

• Co-Infection of HIV, tuberculosis, influenza virus, adenovirus, and other respiratory infection viruses

• Patients with a previous history of pulmonary embolism

• Be thought by researchers to be inappropriate to participate in this clinical study (Expected deaths within 48 hours, uncontrolled infections)

• Liver or kidney SOFA score of more than 3 points; combined with other organ failures (need organ support), Stage 4 severe chronic kidney disease or requiring dialysis (i.e. estimated glomerular filtration rate (eGFR) < 30)

• Pulmonary obstructive pneumonia, severe pulmonary interstitial fibrosis, alveolar proteinosis, allergic alveolitis, and other known viral pneumonia or bacterial pneumonia

• Continuous use of immunosuppressive agents or organ transplants in the past 6 months

• In vitro life support (ECMO, ECCO2R, RRT)

• Pregnant or lactating women

• Uncontrolled underlying disease

Related Conditions & MeSH terms

• Acute Lung Injury
• Covid-19
• Respiratory Distress Syndrome, Adult
• Respiratory Distress Syndrome, Newborn

Intervention

Biological:
• Cell therapy protocol 1
Cell therapy protocol 1(n=20). Patients will receive two doses of MSCs 100×10e6 (±10%) at Day 0 and Day 2 plus Conventional treatment.
• Cell therapy protocol 2
Patients will receive two doses of MSCs 100×10e6 (±10%)at Day 0 and Day 2, intravenously plus two doses of EVs at Day 4 and Day 6 plus conventional treatment.

Locations

Country	Name	City	State
Iran, Islamic Republic of	Royan Institute	Tehran

Sponsors (3)

Lead Sponsor	Collaborator
Royan Institute	Shahid Beheshti University of Medical Sciences, Tehran University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adverse events assessment	Number of participants with treatment-related adverse events as assessed by CTCAE v4.0	From baseline to day 28
Primary	Blood oxygen saturation	Evaluation of Pneumonia Improvement	From baseline to day 14
Secondary	Intensive care unit-free days	Number of days	Up to day 8
Secondary	Clinical symptoms	Improvement of clinical symptoms including duration of fever, respiratory distress, pneumonia, cough, sneezing	From baseline to day 14
Secondary	Respiratory efficacy	increase in PaO2/FiO2 ratio from baseline to day 7	From baseline to day 7
Secondary	Biomarkers concentrations in plasma	Biochemical examination	At baseline, 7, 14, 28 days after the first intervention