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Mesoblast LimitedASX: MSB

FDA Clears IND for Remestemcel Use in COVID-19 ARDS Patients

Apr 5, 2020 at 11:30 PM EDT · Issued by Mesoblast Limited

Filed with ASX · Apr 5, 2020 at 11:30 PM EDT

On 6ix: 6ix.com/news/fda-clears-ind-for-remestemcel-use-in-covid-19-ards-patients

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Earlier from Mesoblast

  • FDA Accepts BLA for RYONCIL and Agrees to Priority ReviewMar 31, 2020
  • Mesoblast to Evaluate Remestemcel-L in COVID-19 Lung DiseaseMar 9, 2020
  • Mesoblast Provides Half Year Results and Corporate UpdateFeb 26, 2020
  • Mesoblast Submits Completed BLA for Ryoncil to US FDAFeb 2, 2020
  • Appendix 4C - quarterlyJan 28, 2020

Later from Mesoblast

  • US NIH Trials Network to Conduct COVID-19 Phase 2/3 TrialApr 8, 2020
  • 83% Survival in COVID-19 ARDS Patients with Remestemcel-LApr 24, 2020
  • Phase 2/3 Trial in COVID-19 ARDS Begins EnrollmentApr 29, 2020
  • MSB Completes Financing For Covid-19 ARDS ManufacturingMay 13, 2020
  • Remestemcel-L Improves Outcomes in Inflammatory Lung DiseaseJun 1, 2020
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