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Mesoblast reports FY25 net loss ($102.1M) vs. ($88.0M) last year

Reports FY25 revenue $17.2M vs. $5.9M last year. Mesoblast (MESO) CEO Dr. Silviu Itescu said, “This has been a banner year for the Company, with achievement of FDA approval for Ryoncil, the first and only FDA approved mesenchymal stromal cell, MSC, product in the United States and a successful commercial launch of the product for treatment of steroid-refractory acute graft-versus-host disease in pediatric patients aged 2 months and older. We are working tirelessly to transform Mesoblast into a fast-paced commercial biotechnology company with demonstrable sales of our first commercial product Ryoncil. We intend to deliver additional approved indications for sales of Ryoncil and to launch a next-generation platform technology into potential blockbuster indications including heart failure and chronic low back pain.”

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