FDA
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Ryoncil® Delivers Net Revenue of US$36M for the Fourth Quarter Ended 30 June 2026
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Mesoblast Receives IND Clearance From FDA to Directly Proceed to Registrational Trial for Approval of Ryoncil® in Duchenne Muscular Dystrophy - CORRECTION
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Ryoncil® Net Revenues Increase for the Quarter to US$30M
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Independent Study Presented at American Society of Hematology (ASH) Annual Meeting Concludes Remestemcel-L Superior to Ruxolitinib in Clinical Outcomes as Treatment for SR-aGvHD
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Ryoncil® Receives J-Code From Medicare & Medicaid Services (CMS) Facilitating Reimbursement and Broader Patient Access
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Mesoblast Maintains Momentum With FDA on Accelerated Approval Pathway for Revascor® in Ischemic Heart Failure and Label Extension for Ryoncil® in Adults With GvHD
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First Three Children to Commence Treatment With Ryoncil®
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329,890 total articles have been posted to this entity.
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