Grafix® Featured in Plenary Session Oral Presentation at the Joint Annual Meeting of the Eastern and New England Vascular Societies

Osiris Therapeutics, Inc. (NASDAQ: OSIR), announced today that data from an evaluation of Grafix in the treatment of chronic venous leg ulcers (VLUs) was presented on Sunday September 14th, at the joint annual meeting of the Eastern Vascular Society and the New England Society for Vascular Surgery.

The data, presented by Shahab Toursavadkohi, MD, Assistant Professor of Vascular Surgery at the University of Maryland School of Medicine, highlighted the initial experience of Grafix in the treatment of chronic venous ulcers of at least 12 weeks duration that failed standard compression therapy for at least 6 weeks. Patients with an active infection were excluded from treatment. The interim study analysis evaluated 18 wounds treated with Grafix and compression therapy compared to 13 case matched control wounds with similar wound area and wound age treated with standard compression therapy alone. Overall healing rates in the Grafix patients were 50% compared to 15.4% in the control group (p < 0.05). In addition, patients in the Grafix group had significantly reduced mean time to complete healing (11.9 weeks vs 29.9 weeks, p < 0.05) and mean length of therapy (12.6 weeks vs 106.3 weeks, p=0.015) compared to the compression only group. The on-going evaluation will include up to 50 total patients.

“The data obtained thus far supports the published data available on Grafix in the treatment of venous ulcers,” said senior author Brajesh Lal, MD, Professor of Vascular Surgery at the University of Maryland School of Medicine and Chief of Vascular Surgery, Baltimore VA Medical Center. “These wounds are very difficult to treat and refractory to standard of care approaches. They account for significant morbidity and added costs to the healthcare system. Having new and innovative cellular approaches to treating VLUs allows clinicians the opportunity to improve the lives of the patients we treat while simultaneously lowering overall healthcare costs incurred due to otherwise unsuccessful interventions.”

The Eastern Vascular Society and the New England Society for Vascular Surgery Annual Meeting was held from September 11th to 14th. The meeting represented the first time the two societies held a joint annual meeting, and took place in Boston, MA.

About Venous Leg Ulcers

Venous leg ulcers, which occur when there is congestion of the venous system leading to vascular permeability and local tissue damage, account for over 2.3 million chronic wounds in the US. The ulcers often form on the sides of lower leg above the ankle and below the calf and cost the US healthcare system up to $5 billion annually.

About Grafix

Grafix is a cryopreserved placental membrane for acute and chronic wounds. It is a flexible, conforming membrane that is applied directly at the site of the wound. Grafix is produced by Osiris’ BioSmartTM Intelligent Tissue Processing which maintains the integrity of the extracellular matrix, growth factors, and endogenous fibroblasts, epithelial cells and mesenchymal stem cells of the native tissue.

About Osiris Therapeutics

Osiris Therapeutics, Inc. is the leading stem cell company, having developed the world’s first approved stem cell drug, remestemcel-L for graft versus host disease. Osiris’ products include Grafix, a cryopreserved placental membrane for acute and chronic wounds, Cartiform®, a viable cartilage mesh for cartilage repair and the latest addition to Osiris’ line of products, OvationOS®, a viable bone matrix for bone repair and regeneration. Osiris is a fully integrated company with capabilities in research, development, manufacturing and distribution. Osiris has developed an extensive intellectual property portfolio to protect the company's technology and commercial interests.

Osiris, Grafix, Cartiform and OvationOS are registered trademarks of Osiris Therapeutics, Inc. More information can be found on the company's website, www.Osiris.com. (OSIR-G)

Forward-Looking Statements

This press release contains forward-looking statements. Forward-looking statements include statements about our expectations, beliefs, plans, objectives, intentions, assumptions and other statements that are not historical facts. Words or phrases such as "anticipate," "believe," "continue," "ongoing," "estimate," "expect," "intend," "may," "plan," "potential," "predict," "project" or similar words or phrases, or the negatives of those words or phrases, may identify forward-looking statements, but the absence of these words does not necessarily mean that a statement is not forward-looking. Examples of forward-looking statements may include, without limitation, statements regarding any of the following: our product development efforts; our clinical trials and anticipated regulatory requirements, and our ability to successfully navigate these requirements; the success of our product candidates in development; status of the regulatory process for our product and product candidates; implementation of our corporate strategy; our financial performance; our product research and development activities and projected expenditures, including our anticipated timeline and clinical strategy for marketed Biosurgery products (including Grafix, Ovation, OvationOS and Cartiform) and Biosurgery products under development; our cash needs; patents, trademarks and other proprietary rights; the safety and ability of our products and potential products to address medical needs; our ability to supply a sufficient amount of our marketed products or product candidates and, if approved or otherwise commercially available products, to meet demand; our costs to comply with governmental regulations; our plans for sales and marketing; our plans regarding facilities; types of regulatory frameworks we expect will be applicable to our products and potential products; and results of our scientific research. Additional risks and uncertainties related to the sale of our ceMSC assets and the related transactions contemplated by the Purchase Agreement with Mesoblast include typical business transactional risks, the risk of changing relationships with customers, suppliers or employees, the risk associated with the disposition of our ceMSC assets and the increased relative dependence on and importance of our other business including our Biosurgery business, the risk that we may not be able to fully benefit from the transactions through milestone payments or royalties, payment risks, including the risk associated with receipt of equity as consideration, in lieu of cash, and the risk of dependence on others to achieve results upon which milestone or royalty payments to us are conditioned. Forward-looking statements are subject to known and unknown risks and uncertainties and are based on potentially inaccurate assumptions that could cause actual results to differ materially from those expected or implied by the forward-looking statements. Our actual results could differ materially from those anticipated in forward-looking statements for many reasons, including the factors described in the section entitled "Risk Factors" in our Annual Report on Form 10-K and other Periodic Reports filed on Form 10-Q, with the United States Securities and Exchange Commission. Accordingly, you should not unduly rely on these forward-looking statements. We undertake no obligation to publicly revise any forward-looking statement to reflect circumstances or events after the date of this press release or to reflect the occurrence of unanticipated events.

Contacts:

Osiris Therapeutics, Inc.
Amanda Badillo, 443-545-1834
OsirisPR@Osiris.com

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