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Mesoblast R&D Day Features Significant Commercial Progress & Platform Innovation
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Mesoblast Receives IND Clearance from FDA to Directly Proceed to Registrational Trial for Approval of Ryoncil® in Duchenne Muscular Dystrophy
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Mesoblast to Host R&D Day on April 8, 2026
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Dr. Teresa Montagut Appointed as Clinical Development and Medical Affairs Head at Mesoblast
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Ryoncil® Profits Underpinning Substantial Growth Pipeline
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High Survival Rates With Ryoncil® in EIND Program Emphasize Importance of Earlier Use in Both Children and Adults With SR-aGvHD
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Ryoncil® Net Revenues Increase for the Quarter to US$30M
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Real-World Commercial Experience with Ryoncil® Shows 84% Survival of Children with SR-aGvHD After Completing 28-Days of Treatment
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FDA Acknowledges Effects on Pain Intensity Favor Rexlemestrocel-L, Confirms 12-Month Reduction in Back Pain Supports Product Efficacy
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Mesoblast to Meet With FDA Next Month to Discuss Rexlemestrocel-L and Opioid Cessation
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Ryoncil® Net Revenues Increase 69% in Second Quarter Post Launch
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Ryoncil® Revenues Increase 66% in Second Quarter Post Launch
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Ryoncil® Receives J-Code From Medicare & Medicaid Services (CMS) Facilitating Reimbursement and Broader Patient Access
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Mesoblast Cell Therapy Products are Designated U.S. Origin and Not Subject to Tariffs
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Successful Commercial Launch of Ryoncil® Highlighted at Global Healthcare Conferences
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Mesoblast Enters Into Option To Issue US$50 Million Convertible Notes
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Banner Year for Mesoblast With First FDA Product Approval and Successful Commercial Launch of Ryoncil®
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Successful Commercial Launch of Ryoncil®
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Mesoblast Limited (MSB) received seven years of orphan-drug exclusive approval from US FDA
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FDA Provides Seven Years of Orphan-Drug Exclusive Approval for Ryoncil®
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Appendix 4c Quarterly Activity Report for Quarter Ended March 31, 2025
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First Three Children to Commence Treatment With Ryoncil®
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Ryoncil® Product Information Now Available in All Four Major Drug Pricing Compendia in United States
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Mesoblast Added to S&P/ASX 200 INDEX
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Mesoblast Sets Ryoncil® Price Based on Economic Value of Treatment With Planned Product Availability This Quarter
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Mesoblast Financial Results and Corporate Update Webcast
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Dr. Gregory George MD PhD Joins Mesoblast Board
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Presenting on the Emerging Growth Conference 79 Day 2 on February 19 Register Now
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Ryoncil® FDA Approval and Market Launch Highlighted at Tandem Transplantation Meetings
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Ryoncil® Commercial Launch Update and Product Pipeline
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Appendix 4C Quarterly Activity Report for Quarter Ended December 31, 2024
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Mesoblast’s RYONCIL® is the First U.S. FDA-Approved Mesenchymal Stromal Cell (MSC) Therapy
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FDA Grants Revascor® (Rexlemestrocel-L) Regenerative Medicine Advanced Therapy (RMAT) Designation in Children with Congenital Heart Disease
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Revascor Improves Survival and Reduces Major Morbidity in High-Risk Ischemic Heart Failure Patients With Inflammation
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Appendix 4C Quarterly Activity Report for Quarter Ended September 30, 2024
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Mesoblast Option to Issue Up to US$50 Million Convertible Notes for Product Launch
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Mesoblast Reports Financial Results and Operational Update for Fiscal Year Ended June 30, 2024
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Mesoblast Financial Results and Corporate Update Webcast
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Appendix 4C Quarterly Activity Report for Quarter Ended June 30, 2024
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Mesoblast Limited (MESO): FDA Accepts BLA for Ryoncil in Children With Steroid-Refractory Acute Graft-Versus-Host Disease
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FDA Accepts Mesoblast’s Biologics License Application (BLA) for Ryoncil® in Children With Steroid-Refractory Acute Graft-Versus-Host Disease (SR-aGVHD)
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Patient Enrollment Commenced in Pivotal Phase 3 Trial of Rexlemestrocel-L for Chronic Low Back Pain
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Mesoblast Resubmits Biologics License Application (BLA) with United States Food & Drug Administration (FDA) for Approval of Ryoncil® in Children with Steroid-Refractory Acute Graft-Versus-Host Di
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Mesoblast to File Biologics License Application for Ryoncil® FDA Approval Next Week
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Mesoblast Corporate Presentation at Investor Conference
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Appendix 4c Quarterly Activity Report for Quarter Ended March 31, 2024
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United States Food & Drug Administration (FDA) Notifies Mesoblast that Available Clinical Data from Phase 3 Trial Appear Sufficient to Support BLA Submission for Remestemcel-L in Children with Ste
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Mesoblast Successfully Completes Placement and Accelerated Entitlement Offer
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Mesoblast (MSB) FDA Supports Accelerated Approval Pathway for Rexlemestrocel-L
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United States Food & Drug Administration (FDA) Supports Accelerated Approval Pathway for Rexlemestrocel-L in End-Stage Heart Failure Patients with a Left Ventricular Assist Device (LVAD)
