A Pilot Clinical Study on Inhalation of Mesenchymal Stem Cells Exosomes Treating Severe Novel Coronavirus Pneumonia

Coronavirus Clinical Trial

Official title:

A Pilot Clinical Study on Aerosol Inhalation of the Exosomes Derived From Allogenic Adipose Mesenchymal Stem Cells in the Treatment of Severe Patients With Novel Coronavirus Pneumonia

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04276987
• Other study ID #: MEXCOVID
• Status: Completed
• Phase: Phase 1
• Start date: February 15, 2020
• Est. completion date: July 31, 2020

Study information

• Verified date: September 2020
• Source: Ruijin Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In December 2019, a novel coronavirus infectious disease characterized by acute respiratory impairment due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) broke out in Wuhan city of Hubei province in China. So far no specific antiviral therapy can be available for patients with SARS-CoV-2 infection. Although symptomatic and supportive care, even with mechanical ventilation or extracorporeal membrane oxygenation (ECMO), are strongly recommended for severe infected individuals, those with advancing age and co-morbidities such as diabetes and heart disease remain to be at high risk for adverse outcomes. This pilot clinical trial will be performed to explore the safety and efficiency of aerosol inhalation of the exosomes derived from allogenic adipose mesenchymal stem cells (MSCs-Exo) in severe patients with novel coronavirus pneumonia (NCP).

Description:

Since December 2019, SARS-CoV-2 infection has become a worldwide urgent public health event, especially in China. As of February 13, 2020, over 63,000 cases have been confirmed with over 10,200 severe cases in mainland of China. There is currently no vaccine or specific antiviral treatment existing for SARS-CoV-2 infection. Although symptomatic and supportive care are recommended for severe infected individuals, those with advancing age and co-morbidities such as diabetes and heart disease remain to be at high risk for adverse outcomes, with mortality of ~10%. Therefore, it is urgent to find a safe and effective therapeutic approach to patients with severe coronavirus disease-19(COVID-19) characterized by an severe acute respiratory impairment.

Experimental studies have demonstrated that mesenchymal stem cells (MSCs) or their exosomes (MSCs-Exo) significantly reduced lung inflammation and pathological impairment resulting from different types of lung injury. In addition, macrophage phagocytosis, bacterial killing and outcome are improved. It is highly likely that MSCs-Exo have the same therapeutic effect on inoculation pneumonia as MSCs themselves.

Although human bone marrow MSCs have been safely administered in patients with ARDS and septic shock (phase I/II trials), it seems safer to deliver MSCs-Exo rather than live MSCs. The intravenous administration of MSCs may result in aggregating or clumping in the injured microcirculation and carries the risk of mutagenicity and oncogenicity, which do not exist by treating with nebulized MSCs-Exo. Another advantage of MSCs-Exo over MSCs is the possibility of storing them for several weeks/months allowing their safe transportation and delayed therapeutic use.

The purpose of this single-arm design, open label, combined interventional clinical trial, therefore, is to explore the safety and efficiency of aerosol inhalation of the exosomes derived from allogenic adipose mesenchymal stem cells (MSCs-Exo) in the treatment of severe patients hospitalized with novel coronavirus pneumonia (NCP).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: July 31, 2020
• Est. primary completion date: May 31, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1.Willingness of study participant to accept this treatment arm, and signed informed consent; 2.Male or female, aged at 18 years (including) to 75 years old; 3.Patients with confirmed novel coronavirus pneumonia; 4.Confirmation of SARS-CoV-2 infection by reverse-transcription polymerase chain reaction (RT-PCR) from respiratory tract or blood specimens; 5.Diagnostic criteria of "Severe" or " Critical":

1. Severe, comply with any of the following:

1. Respiratory distress, Respiratory rate (RR) = 30 times/min

2. Pulse oxygen saturation (SpO2) at rest = 93%

3. Partial pressure of oxygen/fraction of inspired oxygen (PaO2/FiO2) = 300mmHg

2. Critical, comply with any of the following:

1. Respiratory failure, and requirement for mechanical ventilation

2. Shock

3. Other organ failure and requirement for ICU monitoring

Exclusion Criteria:

1. Allergic or hypersensitive to any of the ingredients;

2. Pneumonia caused by bacteria, mycoplasma, chlamydia, legionella, fungi or other viruses;

3. Obstructive HABP/VABP induced by lung cancer or other known causes;

4. Carcinoid syndrome;

5. History of long-term use of immunosuppressive agents;

6. History of epilepsy and requirement for continuous anticonvulsant treatment or anticonvulsant treatment received within the last 3 years;

7. History of severe chronic respiratory disease and requirement for long-term oxygen therapy;

8. Undergoing hemodialysis or peritoneal dialysis;

9. Estimated or actual rate of creatinine clearance < 15 ml/min;

10. History of moderate and severe liver disease (Child-Pugh score >12);

11. Expectation of receiving any of following medications during the study:

1. Receiving continuous valproic acid or sodium valproate within the first 2 weeks prior to screening

2. Receiving 5-transtryptamine reuptake inhibitors, tricyclic antidepressants, 5-HT1 receptor agonists or monoamine oxidase inhibitors within the first 2 weeks prior to screening

12. Incapable of understanding study protocol;

13. History of deep venous thrombosis or pulmonary embolism within the last 3 years;

14. Undergoing ECMO or high-frequency oscillatory ventilation support;

15. HIV, hepatitis virus, or syphilis infection;

16. Period of pregnancy or lactation, or planned pregnancy within 6 months;

17. Any condition of unsuitable for the study determined by investigators.

Related Conditions & MeSH terms

• Coronavirus
• Coronavirus Infections
• Pneumonia

Intervention

Biological:
• MSCs-derived exosomes
5 times aerosol inhalation of MSCs-derived exosomes (2.0*10E8 nano vesicles/3 ml at Day 1, Day 2, Day 3, Day 4, Day 5).

Locations

Country	Name	City	State
China	Ruijin Hospital Shanghai Jiao Tong University School of Medicine	Shanghai	Shanghai

Sponsors (4)

Lead Sponsor	Collaborator
Ruijin Hospital	Cellular Biomedicine Group Ltd., Shanghai Public Health Clinical Center, Wuhan Jinyintan Hospital, Wuhan, China

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Sequential organ failure assessment (SOFA) score	Records of daily sequential organ failure assessment (SOFA) score (From 0 to 24 points, higher scores mean a worse outcome)	Every day for 28 days
Other	Lymphocyte Count (10E9/L)	Records of Blood routine test	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	C-reactive protein (CRP) (mg/L)		Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	Lactate dehydrogenase (U/L)		Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	D-dimer (mg/L)	Coagulation function	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	pro-type B natriuretic peptide (pro-BNP) (pg/ml)	Records of heart failure	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	IL-1ß (pg/ml)	Record of serum cytokine	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	IL-2R (ng/L)	Record of serum cytokine	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	IL-6 (ng/L)	Record of serum cytokine	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	IL-8 (ng/L)	Record of serum cytokine	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	Chest imaging	Computed tomography or X-ray	Day0, Day3, Day7, Day14, Day21, Day28, indicated time points can be added if available
Other	Time to SARS-CoV-2 RT-PCR negativity	Time to SARS-CoV-2 RT-PCR negativity in respiratory tract specimens	Up to 28 days
Primary	Adverse reaction (AE) and severe adverse reaction (SAE)	Safety evaluation within 28 days after first treatment, including frequency of adverse reaction (AE) and severe adverse reaction (SAE)	Up to 28 days
Primary	Time to clinical improvement (TTIC)	Efficiency evaluation within 28 days, including time to clinical improvement (TTIC)	Up to 28 days
Secondary	Number of patients weaning from mechanical ventilation	Number of patients weaning from mechanical ventilation within 28 days	Up to 28 days
Secondary	Duration (days) of ICU monitoring	Duration (days) of ICU monitoring within 28 days	Up to 28 days
Secondary	Duration (days) of vasoactive agents usage	Duration (days) of vasoactive agents using within 28 days	Up to 28 days
Secondary	Duration (days) of mechanical ventilation supply	Duration (days) of mechanical ventilation supply among survivors	Up to 28 days
Secondary	Number of patients with improved organ failure	Number of patients with improved organ failure within 28 days, including cardiovascular system, coagulation system, liver, kidney and other extra-pulmonary organs	Up to 28 days
Secondary	Rate of mortality	Rate of mortality within 28 days	Up to 28 days