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Mesoblast Limited (MESO) Enters Global Collaboration with Novartis (NVS)
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Mesoblast Enters Global Collaboration for Development, Manufacture and Commercialization of Remestemcel-L
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Mesoblast Corporate Update and Financial Results Webcast
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Mesoblast (MESO) Reports 2nd Interim Analysis of Clinical Outcomes After 135 Patients Results in Recommendation to Continue Remestemcel-L Phase 3 Trial in COVID-19 ARDS
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Second Interim Analysis of Clinical Outcomes After 135 Patients Results in Recommendation to Continue Remestemcel-L Phase 3 Trial in COVID-19 ARDS
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UPDATE: Mesoblast Limited (MESO) Begins Randomized Controlled Study Using Direct Injection of Remestemcel-L into Inflamed Gut of Patients With Crohn's Disease & Ulcerative Colitis
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Randomized Controlled Study Using Direct Injection of Remestemcel-L Into Inflamed Gut of Patients With Crohn’s Disease and Ulcerative Colitis
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Mesoblast Limited (MESO) Reports Over 50% Enrollment in Randomized Controlled Phase 3 Trial of Remestemcel-L for Reduced Mortality in COVID-19 Acute Respiratory Distress Syndrome
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Randomized Controlled Phase 3 Trial of Remestemcel-L for Reduced Mortality in COVID-19 Acute Respiratory Distress Syndrome Surpasses 50% Enrollment
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Mesoblast Receives Complete Response Letter From the FDA for Biologics License Application for Steroid-Refractory Acute Graft Versus Host Disease in Children
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Mesoblast Wins 2020 Fierce Biotech Innovation of the Year Award for remestemcel-L
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Data Safety Monitoring Board Recommends Continuation of Remestemcel-L Phase 3 Trial in COVID-19 Patients With Acute Respiratory Distress Syndrome
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Mesoblast Limited (MESO) Granted Ethics Approval for Phase 3 Randomized Controlled Trial of Remestemcel-L to Treat COVID-19 Patients in Australia
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Mesoblast Receives Ethics Approval to Treat COVID-19 Patients in Australia
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Mesoblast Reports Substantial Operational Progress and Financial Results for the Year Ended June 30, 2020
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Mesoblast 2020 Full Year Financial Results Webcast
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Mesoblast (MESO) Confirms U.S. FDA Advisory Committee Votes Nine to One in Favor of Remestemcel-L for Efficacy in Children With SR-aGVHD
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U.S. FDA Advisory Committee Votes Nine to One in Favor of Remestemcel-L (Ryoncil™) for Efficacy in Children With Steroid-Refractory Acute Graft Versus Host Disease
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Mesoblast (MESO) Announces Update on Scheduled FDA Advisory Committee Meeting
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Update on Scheduled FDA Advisory Committee Meeting
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Mesoblast Provides Remestemcel-L Update and Quarterly Activity Report
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Executive Leadership Expanded Ahead of First Potential U.S. Product Launch
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Mesoblast Limited (MESO) Announces FDA Advisory Committee Sets Review Date for its remestemcel-L in Pediatric Steroid-Refractory Acute Graft Versus Host Disease
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FDA Advisory Committee Sets Review Date for Mesoblast’s remestemcel-L in Pediatric Steroid-Refractory Acute Graft Versus Host Disease
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Expanded Access Protocol Initiated for Compassionate Use of Remestemcel-L in Children With Multisystem Inflammatory Syndrome Associated With COVID-19
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Remestemcel-L Improves Respiratory and Functional Outcomes in Patients With Inflammatory Lung Disease
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Mesoblast Reports Strong Financial Position and Substantial Operational Progress For the Period Ended March 31, 2020
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Mesoblast to Host Analyst Call on Financial Results for Period Ended March 31, 2020
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Clinical Outcomes Using RYONCIL™ (remestemcel-L) in Children and Adults With Severe Inflammatory Graft Versus Host Disease Published in Three Articles in Biology of Blood and Marrow Transplantation
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Mesoblast Successfully Completes Financing to Scale-Up Manufacturing of Remestemcel-L for COVID-19 ARDS
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Mesoblast (MESO) Reports First Patient Dosed in Phase 2/3 Randomized Controlled Trial of Remestemcel-l for COVID-19 Acute Respiratory Distress Syndrome
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First Patients Dosed in Phase 2/3 Randomized Controlled Trial of Mesoblast’s Remestemcel-l for COVID-19 Acute Respiratory Distress Syndrome
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Phase 2/3 Randomized Controlled Trial of Remestemcel-L in 300 Patients With COVID-19 Acute Respiratory Distress Syndrome Begins Enrollment
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Mesoblast Limited (MESO) Reports 83% survival in ventilator-dependent COVID-19 patients
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83% Survival in COVID-19 Patients with Moderate/Severe Acute Respiratory Distress Syndrome Treated in New York with Mesoblast’s Cell Therapy Remestemcel-L
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Mesoblast to Present Positive Clinical Outcomes Using Remestemcel-L in Patients With Inflammatory Lung Disease at 2020 International Society of Cell and Gene Therapy Annual Meeting
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MESOBLAST PARTNERS WITH THE CARDIOTHORACIC SURGICAL TRIALS NETWORK ESTABLISHED BY THE U.S. NATIONAL INSTITUTES OF HEALTH’S NATIONAL HEART, LUNG AND BLOOD INSTITUTE TO CONDUCT RANDOMIZED CONTROLLED T
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Mesoblast (MESO) Granted FDA Clearance NDA to Use Remestemcel-L in Patients with Acute Respiratory Distress Syndrome Caused by COVID-19
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FDA CLEARS INVESTIGATIONAL NEW DRUG APPLICATION FOR MESOBLAST TO USE REMESTEMCEL-L IN PATIENTS WITH ACUTE RESPIRATORY DISTRESS SYNDROME CAUSED BY COVID-19
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UPDATE: Mesoblast Limited (MESO) Reports FDA Acceptance of Biologics License Application for Ryoncil and Agrees to Priority Review
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FDA ACCEPTS MESOBLAST’S BIOLOGICS LICENCE APPLICATION FOR RYONCIL™ AND AGREES TO PRIORITY REVIEW
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CLINICAL OUTCOMES OF MESOBLAST’S CELL THERAPY IN END-STAGE ISCHEMIC HEART FAILURE PRESENTED AT AMERICAN COLLEGE OF CARDIOLOGY VIRTUAL SCIENTIFIC SESSIONS
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Mesoblast Limited (MESO) to Study remestemcel-L for COVID-19 Lung Disease
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Mesoblast To Evaluate Anti-Inflammatory Cell Therapy Remestemcel-L For Treatment Of COVID-19 Lung Disease
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Mesoblast Reports Financial Results and Corporate Highlights for First Half Ended December 31, 2019
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Mesoblast to Host Analyst Call on First Half Financial Results for Period Ended December 31, 2019
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Consistent Outcomes Using Ryoncil™ as First-Line Treatment or Salvage Therapy in 309 Children With Steroid-Refractory Acute GVHD
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Clinically Meaningful Outcomes Using Remestemcel-L In Patients With Chronic Graft Versus Host Disease
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Mesoblast Submits Completed Biologics License Application for Ryoncil™ to US FDA
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Mesoblast Submits Completed Biologics License Application for Ryoncil™ to US FDA

