Official Title
Therapeutic Study to Evaluate the Safety and Efficacy of DW-MSC in COVID-19 Patients: Randomized, Double-blind, and Placebo-controlled
Brief Summary

This is a phase 1 clinical trial to verify the safety and efficacy of DW-MSC in COVID-19 patients. A total of 9 subjects are randomly allocated. Subjects who meet the final inclusion and exclusion criteria are randomized to the test groups (low-dose group and high-dose group) or control group (placebo group) in a ratio of 1:1:1. Subjects assigned to the test groups were administered intravenously once with 5 x 10^7cells of DW-MSC for the low-dose group or 1 x 10^8cells for the high-dose group after registration. Subjects assigned to the control group were administered with placebo in the same manner as the test drug (DW-MSC). At this time, all of the existing standard co-treatment are allowed. DW-MSC is adjunct therapy to standard therapy. This clinical trial is a double-blind trial, in which a randomized method will be used. To maintain the double-blindness of the study, statistician who do not participate in this study independently generate randomization code. Subjects will be randomized to the test groups (low-dose group and high-dose group) or the control group (placebo group) in a 1:1:1 ratio. After the completion of the trial, the randomization code will be disclosed after unlocking the database and unblinding procedures. Follow Up period: observed for 28 days after a single administration

Detailed Description

Patients with Covid-19 have a mortality rate of about 35 ~ 50% and currently, severe patients
caused by the Coronavirus show respiratory distress. To date, the incidence rate has been
more than 3 million each year; however, as the increase and globalization of the
environmental pollution has been expanded, the number of patients is expected to increase due
to acute diseases such as the Middle East Respiratory virus, SARS, and coronavirus.

Since 2015, Daewoong Pharmaceutical intends to use stem cells for product research on rare
and intractable diseases including respiratory distress. Stem cells are also called
pluripotent cells or truncal cells that can convert to any organ. It is an embryonic stage
undifferentiated cell that has stopped differentiating before forming a specific organ whose
differentiation has not been determined and has the ability to differentiate into muscle,
bone, and internal conformal body organs. There are three types of stem cells: embryonic stem
cells, adult stem cells, and induced pluripotent stem cells. Daewoong Pharmaceutical intends
to develop cell therapy products using mesenchymal stem cells (MSC).

Completed
COVID19
Corona Virus Infection
SAR

Drug: allogeneic mesenchymal stem cell

Assignment of Administration Group allogeneic mesenchymal stem cell:
Low-dose group (5 x 10^7cells)
High-dose group (1 x 10^8 cells)
Other Name: Investigational product

Other: Placebo

Control group (placebo)

Eligibility Criteria

Inclusion Criteria:

1. Age of 19 years or older at the time of screening

2. Those who have been confirmed COVID-19 infection through PCR test

3. Patients with mild or moderate COVID-19 who meet National EWS (0~6)

4. Those who have given written consent and voluntarily decided to participate before the
screening procedure after understanding the detailed description of the clinical
trial.

5. Those who are suitable as subjects for this clinical study when judged by physical
examination, clinical laboratory test, and other medical examination as stated in the
flowchart of protocol.

Exclusion Criteria:

1. Those who have history of hypersensitivity to the components of the investigational
product or the reference product

2. Those with viral or bacterial pneumonia other than expected indications

3. Patients receiving organ transplants within 6 months of screening

4. Patients with a history of pulmonary embolism

5. Patients who have indications of investigational products as an underlying disease
(ex. HIV patients in the clinical study of antiretroviral drugs)

6. Patients who are pregnant or lactating

7. Those who are determined by the investigator to be unsuitable for participation in the
clinical trial due to other reasons including the results of the clinical laboratory
test.

8. Patients participating in other clinical studies

Eligibility Gender
All
Eligibility Age
Minimum: 19 Years ~ Maximum: N/A
Countries
Indonesia
Locations

Site 550: University of Hassanudin/ Dr. Wahidin Sudirohusodo Hospital
Makassar, Indonesia

Dr. Muhammad Karyana, MPH, Study Chair
Center for Research and Development of Health Resources and Services, National Institute of Health Research and Development (NIHRD), Indonesia

NCT Number
Keywords
Infectious disease
Covid-19
allogeneic mesenchymal stem cell
MeSH Terms
COVID-19
Coronavirus Infections