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TERMINATED
NCT04367077
PHASE2/PHASE3

MultiStem Administration for COVID-19 Induced ARDS (MACoVIA)

Sponsor: Healios K.K.

View on ClinicalTrials.gov

Summary

Multicenter investigation featuring an open-label lead-in followed by a double blinded, randomized, placebo-controlled Phase 2/3 part to evaluate the safety and efficacy of MultiStem therapy in subjects with moderate to severe Acute Respiratory Distress Syndrome (ARDS) due to pathogens including COVID-19.

Official title: A Phase 2/3 Study to Assess the Safety and Efficacy of MultiStem® Therapy in Subjects With Acute Respiratory Distress Syndrome (ARDS) Due to Coronavirus Disease (COVID-19)

Key Details

Gender

All

Age Range

18 Years - 89 Years

Study Type

INTERVENTIONAL

Enrollment

22

Start Date

2020-04-28

Completion Date

2024-10-01

Last Updated

2026-10-16

Healthy Volunteers

No

Conditions

Interventions

BIOLOGICAL

MultiStem

intravenous infusion

BIOLOGICAL

Placebo

intravenous infusion

Locations (4)

Athersys Investigational Site 107

Chicago, Illinois, United States

Athersys Investigational Site 103

Akron, Ohio, United States

Athersys Investigational Site 101

Cleveland, Ohio, United States

Athersys Investigational Site 102

Cleveland, Ohio, United States