ClinicalTrials.Veeva

Menu

Treatment of COVID-19 Patients Using Wharton's Jelly-Mesenchymal Stem Cells

S

Stem Cells Arabia

Status and phase

Unknown
Phase 1

Conditions

Use of Stem Cells for COVID-19 Treatment

Treatments

Biological: WJ-MSCs

Study type

Interventional

Funder types

Other

Identifiers

NCT04313322
COVID-19

Details and patient eligibility

About

The purpose of this study is to investigate the potential use of Wharton's Jelly Mesenchymal stem cells (WJ-MSCs) for treatment of patient diagnosed with Corona Virus SARS-CoV-2 infection, and showing symptoms of COVID-19.

Full description

COVID-19 is a condition caused by infection with Coronoa Virus (SARS-CoV-2). This virus has a high transmission rate and is spreading at very high rates. causing a worldwide pandemic. Patients diagnosed with COVID-19 and confirmed positive with the virus, will be given three IV doses of WJ-MSCs consisting of 1X10e6/kg. The three doses will be 3 days apart form each other.

Patients will be followed up for a period of three weeks to assess the severity of the condition and measure the viral titers.

Enrollment

5 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

COVID-19 positive according to diagnosis and clinical management of COVID-19 criteria.

Exclusion criteria

  • Participants in other clinical trials
  • patients with malignant tumors
  • pregnant and lactating women
  • co-infection with other infectious viruses or bacteria
  • History of several allergies
  • Patients with history of pulmonary embolism
  • any liver or kidney diseases
  • HIV positive patients
  • Considered by researchers to be not suitable to participate in this clinical trial
  • Chronic heart failure with ejection fraction less than 30%.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

WJ-MSCs
Experimental group
Description:
WJ-MSCs will be derived from cord tissue of newborns, screened for HIV1/2, HBV, HCV, CMV, Mycoplasma, and cultured to enrich for MSCs. WJ-MSCs will be counted and suspended in 25 ml of Saline solution containing 0.5% human serum Albumin, and will be given to patient intravenously.
Treatment:
Biological: WJ-MSCs

Trial contacts and locations

1

Loading...

Central trial contact

Adeeb M AlZoubi, Ph.D.; Ahmad Y AlGhadi, M.Sc.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems