Recruiting
Phase 2

Lung Injury

Sponsor:

Stemedica Cell Technologies, Inc.

Code:

NCT04780685

Conditions

Covid19

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

hMSC

Study Details

Brief summary:

This is a Phase II multi-center, double-blind, placebo-controlled, randomized study in Patients with moderate to severe lung injury due to COVID-19 or other potential viral and bacterial pathogens.

Conditions

Covid19

Study ID

NCT04780685

Start date

Mar 20, 2021

Status verified date

Jul, 2022

Completion date

Dec 31, 2022

Anticipated

Primary completion date

Sep 30, 2022

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Laboratory-confirmed diagnosis of COVID-19 <= 14 days prior to randomization
  • The presence of moderate to severe Acute Respiratory Distress Syndrome (ARDS) as defined by the Berlin Definition:

1. Bilateral chest radiograph infiltrates.
2. PaO2:FiO2 ratio of less than 200.
3. Absence of other clinical conditions that could present in a similar manner (non-infectious pneumonitis, cardiogenic pulmonary edema)
  • Absence of moribund state that would indicate imminent demise and poor chance of survival.

Exclusion Criteria:

  • Females of childbearing potential who are pregnant or unwilling to undergo pregnancy testing; females with a positive pregnancy test on screening day will be excluded.
  • Breastfeeding mothers
  • Patients on ECMO
  • Receiving concurrent treatment with an investigational agent in a clinical trial.
  • Exception: Use of COVID-19 convalescent plasma is permitted.
  • More than 72hrs on mechanical ventilation before randomization
  • Receiving concurrent investigational vaccine

Study Design

Enrollment

40 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: hMSCs

hMSCs will be given via IV administration.

placebo comparator: Lactated Ringer's Solution

Lactated Ringer's Solution will be given via IV administration.

Interventions

hMSC

IV administration

Primary outcome measure

  • Survival [ Time Frame: 14 days post treatment ]

Central Contacts and Locations

Central contacts

Locations

Providence Medical Foundation

Recruiting

Fullerton, California, United States, 92835

Contacts

Principal Investigator:

David Park, MD

Providence Saint John's Health Center - Saint John's Cancer Institute

Recruiting

Santa Monica, California, United States, 90404

Contacts

Principal Investigator:

Santosh Kesari, MD

More Information

Sponsor

Stemedica Cell Technologies, Inc.

Last update posted

Jul 8, 2022

Last verified

Jul, 2022

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Stemedica Cell Technologies, Inc. on 2022-07-08.