http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View More Recent Stories
-
Mesoblast 2020 Full Year Financial Results Webcast
-
Mesoblast (MESO) Confirms U.S. FDA Advisory Committee Votes Nine to One in Favor of Remestemcel-L for Efficacy in Children With SR-aGVHD
-
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
-
Mesoblast (MESO) Announces Update on Scheduled FDA Advisory Committee Meeting
-
Update on Scheduled FDA Advisory Committee Meeting
-
Mesoblast Provides Remestemcel-L Update and Quarterly Activity Report
-
Executive Leadership Expanded Ahead of First Potential U.S. Product Launch
-
Mesoblast Limited (MESO) Announces FDA Advisory Committee Sets Review Date for its remestemcel-L in Pediatric Steroid-Refractory Acute Graft Versus Host Disease
-
FDA Advisory Committee Sets Review Date for Mesoblast’s remestemcel-L in Pediatric Steroid-Refractory Acute Graft Versus Host Disease
-
Expanded Access Protocol Initiated for Compassionate Use of Remestemcel-L in Children With Multisystem Inflammatory Syndrome Associated With COVID-19
-
Remestemcel-L Improves Respiratory and Functional Outcomes in Patients With Inflammatory Lung Disease
-
Mesoblast Reports Strong Financial Position and Substantial Operational Progress For the Period Ended March 31, 2020
-
Mesoblast to Host Analyst Call on Financial Results for Period Ended March 31, 2020
-
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
-
Mesoblast Successfully Completes Financing to Scale-Up Manufacturing of Remestemcel-L for COVID-19 ARDS
-
Mesoblast (MESO) Reports First Patient Dosed in Phase 2/3 Randomized Controlled Trial of Remestemcel-l for COVID-19 Acute Respiratory Distress Syndrome
-
First Patients Dosed in Phase 2/3 Randomized Controlled Trial of Mesoblast’s Remestemcel-l for COVID-19 Acute Respiratory Distress Syndrome
-
Phase 2/3 Randomized Controlled Trial of Remestemcel-L in 300 Patients With COVID-19 Acute Respiratory Distress Syndrome Begins Enrollment
-
Mesoblast Limited (MESO) Reports 83% survival in ventilator-dependent COVID-19 patients
-
83% Survival in COVID-19 Patients with Moderate/Severe Acute Respiratory Distress Syndrome Treated in New York with Mesoblast’s Cell Therapy Remestemcel-L
-
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
-
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
-
Mesoblast (MESO) Granted FDA Clearance NDA to Use Remestemcel-L in Patients with Acute Respiratory Distress Syndrome Caused by COVID-19
-
FDA CLEARS INVESTIGATIONAL NEW DRUG APPLICATION FOR MESOBLAST TO USE REMESTEMCEL-L IN PATIENTS WITH ACUTE RESPIRATORY DISTRESS SYNDROME CAUSED BY COVID-19
-
FDA ACCEPTS MESOBLAST’S BIOLOGICS LICENCE APPLICATION FOR RYONCIL™ AND AGREES TO PRIORITY REVIEW
-
CLINICAL OUTCOMES OF MESOBLAST’S CELL THERAPY IN END-STAGE ISCHEMIC HEART FAILURE PRESENTED AT AMERICAN COLLEGE OF CARDIOLOGY VIRTUAL SCIENTIFIC SESSIONS
-
Mesoblast To Evaluate Anti-Inflammatory Cell Therapy Remestemcel-L For Treatment Of COVID-19 Lung Disease
-
Mesoblast Reports Financial Results and Corporate Highlights for First Half Ended December 31, 2019
-
Mesoblast to Host Analyst Call on First Half Financial Results for Period Ended December 31, 2019
-
Consistent Outcomes Using Ryoncil™ as First-Line Treatment or Salvage Therapy in 309 Children With Steroid-Refractory Acute GVHD
-
Clinically Meaningful Outcomes Using Remestemcel-L In Patients With Chronic Graft Versus Host Disease
-
Mesoblast Submits Completed Biologics License Application for Ryoncil™ to US FDA
-
Mesoblast Submits Completed Biologics License Application for Ryoncil™ to US FDA
-
Mesoblast Presents Commercial Plans at 2020 Biotech Showcase in San Francisco
-
Mesoblast Submits Clinical Efficacy And Safety Data To FDA In Rolling Biologics License Application For Remestemcel-L
-
Data Monitoring Committee Completes Final Scheduled Review of Mesoblast’s Phase 3 Trial of Revascor in Advanced Chronic Heart Failure
-
Mesoblast’s Phase 3 Trial of Revascor in Advanced Chronic Heart Failure Surpasses the Number of Primary Endpoint Events for Trial Completion
-
Mesoblast Finanical Results for the Quarter Ended September 30, 2019
-
Mesoblast to Host Analyst Call on Financial Results for First Quarter Ended September 30, 2019
-
Mesoblast and Lonza Enter Into Agreement for Commercial Manufacture of Mesoblast’s Potential First United States Allogeneic Cell Therapy
-
Mesoblast Completes Successful Institutional Capital Raising of A$75 Million

