Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
9

Summary

Conditions
  • ARDS, Human
  • COVID
Type
Interventional
Phase
Phase 1
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: This is an open label, dose escalating safety study of the advanced therapy investigational medicinal product (ATIMP) KI-MSC-PL-205, where patients diagnosed with SARS-CoV-2-induced severe acute respiratory distress syndrome (ARDS).Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 65 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04447833
Collaborators
Uppsala University Hospital
Investigators
Principal Investigator: Oscar Simonsson, MD, PhD Uppsala University