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Clinical Trials/NCT04331613
NCT04331613
Unknown
Phase 1

Safety and Efficacy Study of Human Embryonic Stem Cells Derived M Cells (CAStem) for the Treatment of Severe COVID-19 Associated With or Without Acute Respiratory Distress Syndrome (ARDS)

Chinese Academy of Sciences1 site in 1 country9 target enrollmentJanuary 27, 2020

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
COVID-19
Sponsor
Chinese Academy of Sciences
Enrollment
9
Locations
1
Primary Endpoint
Adverse reaction (AE) and severe adverse reaction (SAE)
Last Updated
6 years ago

Overview

Brief Summary

A phase1/2, open label, dose escalation, safety and early efficacy study of CAStem for the treatment of severe COVID-19 associated with or without ARDS.

Detailed Description

CAStem is an injectable product composed of immunity- and matrix-regulatory cells (IMRCs), also named M cells, differentiated from clinical-grade human embryonic stem cells (hESCs) will be expanded, harvested, and formulated at a concentration of 50 x 10\^6 cells/mL. CAStem will be cryopreserved and transported to clinical site using liquid nitrogen vapor shipping vessels (\< -150ºC). Prior to injection, CAStem will be thawed to liquefy quickly, and then reconstituted in normal saline.In the present study, the intravenous infusion dose of CAStem will be 3, 5 or 10 million cells/kg.

Registry
clinicaltrials.gov
Start Date
January 27, 2020
End Date
December 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Qi Zhou

Director, Institute of Zoology, Chinese Academy of sciences

Chinese Academy of Sciences

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Adverse reaction (AE) and severe adverse reaction (SAE)

Time Frame: Within 28 days after treatment

Frequency of adverse reaction (AE) and severe adverse reaction (SAE) within 28 days after treatment

Changes of lung imaging examinations

Time Frame: Within 28 days after treatment

Evaluation by chest CT

Secondary Outcomes

  • Lymphocyte count (*10^9/L)(Within 28 days after treatment)
  • Creatinine (umol/L)(Within 28 days after treatment)
  • Creatine kinase (U/L)(Within 28 days after treatment)
  • Duration of fever (Celsius)(Within 28 days after treatment)
  • IL-2 (pg/mL)(Within 28 days after treatment)
  • Rate of all-cause mortality within 28 days(Within 28 days after treatment)
  • Time to SARS-CoV-2 RT-PCR negative(Within 28 days after treatment)
  • Alanine aminotransferase (U/L)(Within 28 days after treatment)
  • Lactate (mmol/L)(Within 28 days after treatment)
  • IL-1beta (pg/mL)(Within 28 days after treatment)
  • IL-8 (pg/mL)(Within 28 days after treatment)
  • Changes of blood oxygen (%)(Within 28 days after treatment)
  • C-reactive protein (mg/L)(Within 28 days after treatment)
  • Procalcitonin (ng/L)(Within 28 days after treatment)
  • IL-6 (pg/mL)(Within 28 days after treatment)

Study Sites (1)

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