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Clinical Research of Human Mesenchymal Stem Cells in the Treatment of COVID-19 Pneumonia

Primary Purpose

COVID-19

Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
UC-MSCs
Placebo
Sponsored by
Puren Hospital Affiliated to Wuhan University of Science and Technology
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COVID-19 focused on measuring COVID-19, UC-MSCs, critically ill, cell transplantation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male or female, 18 years old ≤ age ≤ 75years old;
  2. CT image is characteristic of 2019 novel coronavirus pneumonia;
  3. Laboratory confirmation of 2019-nCoV infection by reverse transcription polymerase chain reaction (RT-PCR);
  4. In compliance with the 2019-nCoV pneumonia diagnosis standard (according to the novel coronavirus infection pneumonia diagnosis and treatment program (Trial Implementation Version 6) issued by the National Health and Medical Commission, and WHO 2019 new coronavirus guidelines standards): (A) increased breathing rate (≥30 beats / min), difficulty breathing, cyanosis of the lips; (B) in resting state, means oxygen saturation ≤93%; (C) partial pressure of arterial oxygen (PaO2) / Fraction of inspired oxygen (FiO2) ≤300 mmHg (1mmHg = 0.133kPa);
  5. Participant or the authorized agent signed the informed consent form.
  6. Agree to collect clinical samples.

Exclusion Criteria:

  1. Malignant disease in the past five years;
  2. Participant with no hope of survival were clinically predicted and only received hospice care, or those who were in a deep coma and did not respond to supportive treatment measures within three hours of admission.
  3. Participant who are participating in other clinical trials or who have participated in other clinical trials within 3 months.
  4. Cases of severe shock and respiratory failure.

Sites / Locations

  • Puren Hospital Affiliated to Wuhan University of Science and TechnologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

UC-MSCs treatment group

Control group

Arm Description

Participants will receive conventional and treatment with MSCs, MSCs were suspended in 100 mL of normal saline, and the total number of transplanted cells was calculated by 1*10E6 cells per kilogram of weight. This product is generally a course of treatment, a total of 1 time, depending on the condition of the need to be given again at an interval of 1 week.

Participants will receive conventional treatment and Placebo intravenously.

Outcomes

Primary Outcome Measures

The immune function (TNF-α 、IL-1β、IL-6、TGF-β、IL-8、PCT、CRP)
Improvement and recovery time of inflammatory and immune factors
Blood oxygen saturation
Evaluation of Pneumonia change

Secondary Outcome Measures

Rate of mortality within 28-days
Marker for efficacy of treatment
Size of lesion area by chest imaging
Evaluation of Pneumonia change
CD4+ and CD8+ T cells count
Marker of Immunology and inflammation
Peripheral blood count recovery time
Degree of infection
Duration of respiratory symptoms (fever, dry cough, difficulty breathing, etc.)
Indirect response to lung function
COVID-19 nucleic acid negative time
Clearance time of COVID-19 in participant

Full Information

First Posted
April 2, 2020
Last Updated
April 5, 2020
Sponsor
Puren Hospital Affiliated to Wuhan University of Science and Technology
Collaborators
Shanghai University, Qingdao Co-orient Watson Biotechnology group co. LTD, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT04339660
Brief Title
Clinical Research of Human Mesenchymal Stem Cells in the Treatment of COVID-19 Pneumonia
Official Title
Clinical Research of Human Mesenchymal Stem Cells in the Treatment of COVID-19 Pneumonia
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2020 (Actual)
Primary Completion Date
June 30, 2020 (Anticipated)
Study Completion Date
June 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Puren Hospital Affiliated to Wuhan University of Science and Technology
Collaborators
Shanghai University, Qingdao Co-orient Watson Biotechnology group co. LTD, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The COVID-19 pneumonia has grown to be a global public health emergency since patients were first detected in Wuhan, China, in December 2019, which spread quickly to worldwide and presented a serious threat to public health. It is mainly characterized by fever, dry cough, shortness of breath and breathing difficulties. Some patients may develop into rapid and deadly respiratory system injury with overwhelming inflammation in the lung. Currently, no specific drugs or vaccines are available to cure the patients with COVID-19 pneumonia. Hence, there is a large unmet need for a safe and effective treatment for COVID-19 pneumonia patients, especially the critically ill cases. The significant clinical outcome and well tolerance was observed by the adoptive transfer of allogenic MSCs. We proposed that the adoptive transfer therapy of MSCs might be an ideal choice to be used. We expect to provide new options for the treatment of critically ill COVID-19 pneumonia patients and contribute to improving the quality of life of critically ill patients.
Detailed Description
Since December 2019, novel coronavirus disease 2019 (COVID-19) in Wuhan has been fierce and spread rapidly. As of 24:00 on March 4, 2020, China has reported a total of 80567 confirmed cases, 5952 existing critically ill cases, and 3016 dead cases. The COVID-19 pneumonia has grown to be a global public health emergency since patients were first detected in Wuhan, China, in December 2019, which spread quickly to 26 countries worldwide and presented a serious threat to public health. It is mainly characterized by fever, dry cough, shortness of breath and breathing difficulties. Some patients may develop into rapid and deadly respiratory system injury with overwhelming inflammation in the lung. Currently, no specific drugs or vaccines are available to cure the patients with COVID-19 infection. Hence, there is a large unmet need for a safe and effective treatment for COVID-19 infected patients, especially the critically ill cases. Recently, some clinical researches about the COVID-19 published in The Lancet and The New England Journal of Medicine suggested that massive inflammatory cell infiltration and inflammatory cytokines secretion were found in patients' lungs, alveolar epithelial cells and capillary endothelial cells were damaged, causing acute lung injury. Several reports demonstrated that the first step of the HCoV-19 pathogenesis is that the virus specifically recognizes the angiotensin I converting enzyme 2 receptor (ACE2) by its spike Protein. This receptor is abundant in lung and small intestinal tissues, but is also highly expressed in vascular endothelial cells and smooth muscle cells in almost all organs, including the nervous system and skeletal muscle. The main organ injured by the HCoV-19 is the lung. In fact, HCoV-19 can also involve the nervous system, digestive system, urinary system, blood system and other systems. Therefore, when the initial symptom is discomfort of other systems in the early stage, it is often easy to be misdiagnosed and delay treatment. Moreover, the HCoV-19 is a noncellular form consisting of RNA and protein, which cannot be copied independently. It needs to bind to cell surface receptors to enter the cell to complete the replication, and then be released again. Therefore, once the HCoV-19 enters the blood circulation, it can easily spread to all systems throughout the body, which may be the pathological mechanism that the HCoV-19 directly or indirectly causes neurological symptoms. It seems that the key to cure the COVID-19 pneumonia is to inhibit the inflammatory response, resulting to reduce the damage of alveolar epithelial cells and endothelial cells and repair the function of the lung. MSCs, owing to their powerful immunomodulatory ability, may have beneficial effects on preventing or attenuating the cytokine storm. Mesenchymal stem cells (MSCs) are widely used in basic research and clinical application. They are proved to migrate to damaged tissues, exert antiinflammatory and immunoregulatory functions, promote the regeneration of damaged tissues and inhibit tissue fibrosis. MSCs play a positive role mainly in two ways, namely immunomodulatory effects and differentiation abilities. MSCs can secrete many types of cytokines by paracrine secretion or make direct interactions with immune cells, leading to immunomodulation. Studies have shown that MSCs can significantly reduce acute lung injury in mice caused by H9N2 and H5N1 viruses by reducing the levels of proinflammatory cytokines and the recruitment of inflammatory cells into the lungs. Compared with MSCs from other sources, human umbilical cord-derived MSCs (UC-MSCs) have been widely applied to various diseases due to their convenient collection, no ethical controversy, low immunogenicity, and rapid proliferation rate. Here we conducted an MSC transplantation pilot study to explore their therapeutic potential for COVID-19 pneumonia patients. To explore the effective treatment of COVID-19 pneumonia for the current prevention and control of novel coronavirus pneumonia to find a key and effective clinical treatment means, to fight against the epidemic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
Keywords
COVID-19, UC-MSCs, critically ill, cell transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
UC-MSCs treatment group
Arm Type
Experimental
Arm Description
Participants will receive conventional and treatment with MSCs, MSCs were suspended in 100 mL of normal saline, and the total number of transplanted cells was calculated by 1*10E6 cells per kilogram of weight. This product is generally a course of treatment, a total of 1 time, depending on the condition of the need to be given again at an interval of 1 week.
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Participants will receive conventional treatment and Placebo intravenously.
Intervention Type
Biological
Intervention Name(s)
UC-MSCs
Intervention Description
1*10E6 UC-MSCs /kg body weight suspended in 100mL saline
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
100mL saline intravenously
Primary Outcome Measure Information:
Title
The immune function (TNF-α 、IL-1β、IL-6、TGF-β、IL-8、PCT、CRP)
Description
Improvement and recovery time of inflammatory and immune factors
Time Frame
Observe the immune function of the participants within 4 weeks
Title
Blood oxygen saturation
Description
Evaluation of Pneumonia change
Time Frame
Monitor blood oxygen saturation of the participants within 4 weeks
Secondary Outcome Measure Information:
Title
Rate of mortality within 28-days
Description
Marker for efficacy of treatment
Time Frame
At baseline, Day 1, Day 2, Day 7, Week 2, Week 3, Week 4
Title
Size of lesion area by chest imaging
Description
Evaluation of Pneumonia change
Time Frame
At baseline, Day 1, Day 2, Day 7, Week 2, Week 3, Week 4
Title
CD4+ and CD8+ T cells count
Description
Marker of Immunology and inflammation
Time Frame
At baseline, Day 1, Day 2, Day 7, Week 2, Week 3, Week 4
Title
Peripheral blood count recovery time
Description
Degree of infection
Time Frame
At baseline, Day 1, Day 2, Day 7, Week 2, Week 3, Week 4
Title
Duration of respiratory symptoms (fever, dry cough, difficulty breathing, etc.)
Description
Indirect response to lung function
Time Frame
At baseline, Day 1, Day 2, Day 7, Week 2, Week 3, Week 4
Title
COVID-19 nucleic acid negative time
Description
Clearance time of COVID-19 in participant
Time Frame
At baseline, Day 1, Day 2, Day 7, Week 2, Week 3, Week 4

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female, 18 years old ≤ age ≤ 75years old; CT image is characteristic of 2019 novel coronavirus pneumonia; Laboratory confirmation of 2019-nCoV infection by reverse transcription polymerase chain reaction (RT-PCR); In compliance with the 2019-nCoV pneumonia diagnosis standard (according to the novel coronavirus infection pneumonia diagnosis and treatment program (Trial Implementation Version 6) issued by the National Health and Medical Commission, and WHO 2019 new coronavirus guidelines standards): (A) increased breathing rate (≥30 beats / min), difficulty breathing, cyanosis of the lips; (B) in resting state, means oxygen saturation ≤93%; (C) partial pressure of arterial oxygen (PaO2) / Fraction of inspired oxygen (FiO2) ≤300 mmHg (1mmHg = 0.133kPa); Participant or the authorized agent signed the informed consent form. Agree to collect clinical samples. Exclusion Criteria: Malignant disease in the past five years; Participant with no hope of survival were clinically predicted and only received hospice care, or those who were in a deep coma and did not respond to supportive treatment measures within three hours of admission. Participant who are participating in other clinical trials or who have participated in other clinical trials within 3 months. Cases of severe shock and respiratory failure.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yan Liu, MD
Phone
+8613387517458
Email
447822853@qq.com
First Name & Middle Initial & Last Name or Official Title & Degree
Yue Zhu
Phone
+8617786289703
Email
978925651@qq.com
Facility Information:
Facility Name
Puren Hospital Affiliated to Wuhan University of Science and Technology
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430081
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yan Liu, MD
Phone
+8613387517458
Email
447822853@qq.com

12. IPD Sharing Statement

Learn more about this trial

Clinical Research of Human Mesenchymal Stem Cells in the Treatment of COVID-19 Pneumonia

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