Press Releases August 24, 2026 07:00 AM

Mesoblast Financial Results and Corporate Update Webcast

Mesoblast announces financial results webcast and highlights progress in allogeneic cellular medicines for inflammatory diseases

By Marcus Reed
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MESO

Mesoblast Limited, an innovator in allogeneic cellular therapies, will host a webcast to discuss its FY 2026 financial results and operational updates. The company, with products including the FDA-approved Ryoncil® for steroid-refractory acute graft versus host disease, continues to develop multiple therapies for inflammatory and cardiac conditions, supported by extensive global patents and commercial partnerships.

Mesoblast Financial Results and Corporate Update Webcast
MESO
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Key Points

  • Mesoblast is a global leader in allogeneic cellular medicines targeting severe inflammatory diseases, with FDA-approved therapy Ryoncil® for pediatric SR-aGvHD.
  • The company is advancing additional cell therapy indications, including adult SR-aGvHD, inflammatory bowel disease, heart failure, and chronic low back pain.
  • Mesoblast maintains strong intellectual property with over 1,000 patents and has manufacturing capabilities to supply off-the-shelf cellular medicines worldwide, supported by commercial partnerships in Japan, Europe, and China.

NEW YORK, Aug. 24, 2026 (GLOBE NEWSWIRE) -- Mesoblast Limited (ASX:MSB; Nasdaq:MESO), global leader in allogeneic cellular medicines for inflammatory diseases, will host a webcast to discuss operational highlights and financial results for the full year ended June 30, 2026.

The webcast will begin at 6.30pm EDT, Wednesday, August 26; 8.30am AEST, Thursday, August 27, 2026. It can be accessed via: https://webcast.openbriefing.com/msb-fyr-2026/

The archived webcast will be available on the Investor page of the Company’s website: www.mesoblast.com

About Mesoblast
Mesoblast (the Company) is a world leader in developing allogeneic (off-the-shelf) cellular medicines for the treatment of severe and life-threatening inflammatory conditions. The therapies from the Company’s proprietary mesenchymal lineage cell therapy technology platform respond to severe inflammation by releasing anti-inflammatory factors that counter and modulate multiple effector arms of the immune system, resulting in significant reduction of the damaging inflammatory process.

Mesoblast’s Ryoncil® (remestemcel-L-rknd) for the treatment of steroid-refractory acute graft versus host disease (SR-aGvHD) in pediatric patients 2 months and older is the first FDA-approved mesenchymal stromal cell (MSC) therapy. Please see the full Prescribing Information at www.ryoncil.com.

Mesoblast is committed to developing additional cell therapies for distinct indications based on its remestemcel-L and rexlemestrocel-L allogeneic stromal cell technology platforms. Ryoncil® is being developed for additional inflammatory diseases including SR-aGvHD in adults and biologic-resistant inflammatory bowel disease. Rexlemestrocel-L is being developed for heart failure and chronic low back pain. The Company has established commercial partnerships in Japan, Europe and China.

About Mesoblast intellectual property: Mesoblast has a strong and extensive global intellectual property portfolio, with over 1,000 granted patents or patent applications covering mesenchymal stromal cell compositions of matter, methods of manufacturing and indications. These granted patents and patent applications provide commercial protection extending through to at least 2044 in all major markets.

About Mesoblast manufacturing: The Company’s proprietary manufacturing processes yield industrial-scale, cryopreserved, off-the-shelf, cellular medicines. These cell therapies, with defined pharmaceutical release criteria, are planned to be readily available to patients worldwide.

Mesoblast has locations in Australia, the United States and Singapore and is listed on the Australian Securities Exchange (MSB) and on the Nasdaq (MESO). For more information, please see www.mesoblast.com, LinkedIn: Mesoblast Limited and X: @Mesoblast

Release authorized by the Chief Executive.

For more information, please contact:

Corporate Communications / Investors Paul Hughes T: +61 3 9639 6036   Media – GlobalMedia – AustraliaRubensteinBlueDot MediaCaroline NelsonSteve DabkowskiT: +1 703 489 3037T: +61 419 880 486E: [email protected][email protected]

Risks

  • Therapeutic development and approval processes for new indications involve clinical and regulatory risk that could affect product commercialization timelines.
  • Market adoption and reimbursement challenges in various geographies might impact the commercial performance of Mesoblast’s therapies.
  • Manufacturing scale-up and supply chain reliability are critical for global distribution and could pose operational risks if disrupted.

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