Mesoblast’s Ryoncil® Gains FDA Approval, Set to Revolutionize SR-aGvHD Treatment

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Mesoblast’s Ryoncil® Gains FDA Approval, Set to Revolutionize SR-aGvHD Treatment

The latest update is out from Mesoblast Limited ( (AU:MSB) ).

Mesoblast Limited announced the FDA approval and upcoming market launch of Ryoncil® (remestemcel-L) at the Transplantation & Cellular Therapy Tandem Meetings. Ryoncil® is the first mesenchymal stromal cell therapy approved in the U.S. for pediatric steroid-refractory acute graft-versus-host disease (SR-aGvHD) and is expected to enhance Mesoblast’s market position in cellular medicines. The product’s approval marks a significant milestone for the company, highlighting its leadership in the field and potential impact on patient care and industry standards.

More about Mesoblast Limited

Mesoblast Limited is a global leader in developing allogeneic cellular medicines, focusing on treating severe inflammatory conditions. Utilizing proprietary mesenchymal lineage cell therapy technology, the company targets severe inflammation with anti-inflammatory factors. Mesoblast has a robust intellectual property portfolio and commercial partnerships in major markets like Japan, Europe, and China. The company is listed on the Australian Securities Exchange and Nasdaq.

YTD Price Performance: -26.36%

Average Trading Volume: 250,258

Technical Sentiment Consensus Rating: Strong Sell

Current Market Cap: $2.37B

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