Bone Marrow-Derived Mesenchymal Stem Cell Treatment for Severe Patients With Coronavirus Disease 2019 (COVID-19)

Guangzhou Institute of Respiratory Disease

Status and phase: Unknown; Phase 2; Phase 1

Conditions: Coronavirus Disease 2019 (COVID-19)

Treatments: Biological: Placebo; Biological: BM-MSCs

Study type: Interventional

Funder types: Other

Identifiers

NCT04346368

SC-2020-01

Details and patient eligibility

About

Coronavirus Disease 2019 (COVID-19) is spreading worldwide and has become a public health emergency of major international concern. Currently, no specific drugs or vaccines are available. For severe cases, it was found that aberrant pathogenic T cells and inflammatory monocytes are rapidly activated and then producing a large number of cytokines and inducing an inflammatory storm.Mesenchymal stem cells (MSCs) have been shown to possess a comprehensive powerful immunomodulatory function. This study aims to investigate the safety and efficacy of intravenous infusion of mesenchymal stem cells in severe patients with COVID-19.

Full description

COVID-19 has become a urgent and serious public health event that threatens human life and health globally. No specific pharmacological treatments are available to date for COVID-19.Patients contracting the severe form of the disease constitute approximately 15% of the cases which is characterized by extensive acute inflammation. In these severe cases, there will be rapid respiratory system failure.

MSCs have been employed extensively in cell therapy, which includes a plethora of preclinical research investigations as well as a significant number of clinical trials. Safety and efficacy have been shown in many clinical trials. Previous studies have shown that MSCs could significantly reduce inflammatory cell infiltration in lung tissue, reduce inflammation in lung tissue, and significantly improve lung The structure and function of tissues protect lung tissue from damage.The mechanisms underlying the improvements after MSC infusion in COVID-19 patients also appeared to be the robust antiinflammatory activity of MSCs. Recent studies also showed that intravenous MSC infusion could reduce the overactivation of the immune system and support repair by modulating the lung microenvironment after SARS-CoV-2 infection. MSC therapy inhibiting the overactivation of the immune system and promoting endogenous repair by improving the lung microenvironment after the SARS-CoV-2 infection.

The purpose of this study is to investigate the safety and efficacy of intravenous infusion of mesenchymal stem cells in severe patients With COVID-19.The respiratory function, pulmonary inflammation, clinical symptoms, pulmonary imaging, side effects, immunological characteristics will be evaluated.

Enrollment: 20 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Willing and able to provide written informed consent prior to performing study procedures

2. Age ≥18 years, and ≤75 years;

   A confirmed case of Covid-19. The criteria are as follows:

   Clinically diagnosed or suspected cases with one of the following etiological evidence: 1) SARS-CoV-2 nucleic acid is positive in respiratory or blood samples detected by RT-PCR; 2) virus sequence detected in respiratory or blood samples shares high homology with the known sequence of SARS-CoV-2.

3. Clinical classification is severe case: Meet any of the following:

1. Increased respiratory rate (≥30 beats / min), difficulty breathing, cyanosis of the lips; 2) Peripheral capillary oxygen saturation (SpO2) ≤93% at rest ; 3)Partial pressure of arterial oxygen (PaO2) / Fraction of inspired oxygen (FiO2) ≤300 mmHg (1mmHg = 0.133kPa).

Exclusion criteria

1. Other types of viral pneumonia, or bacterial pneumonia.
2. The clinical classification is mild, moderate or critical;
3. Patients with malignant blood or solid tumor.
4. Pregnant or lactating women;
5. There are other situations or diseases that the investigator think are not suitable to participate in this clinical study or may be increased risk of the subject.
6. Patients with serious social and mental disability, inability/restriction of legal capacity;
7. Refusal to sign informed consent;
8. Patients with severe liver disease (eg Child Pugh score ≥ C, AST> 5 times upper limit of normal );
9. Patients with severe renal insufficiency (estimated glomerular filtration rate ≤30mL / min / 1.73m2) or receiving continuous renal replacement therapy, hemodialysis, peritoneal dialysis.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

20 participants in 2 patient groups, including a placebo group

Bone Marrow-Derived Mesenchymal Stem Cells (BM-MSCs)

Experimental group

Description:

Conventional treatment plus BM-MSCs

Treatment:

Biological: BM-MSCs

Placebo

Placebo Comparator group

Description:

Conventional treatment plus placebo

Treatment:

Biological: Placebo