Osiris Bolsters its Stem Cell Intellectual Property Estate
COLUMBIA, Md.--(BUSINESS WIRE)--
Osiris
Therapeutics, Inc. (NASDAQ: OSIR), announced today the expansion of
its intellectual property protection around Prochymal® (remestemcel-L).
The United States Patent and Trademark Office recently granted Osiris
two patents that cover multiple mechanisms of action related to cardiac
tissue repair. Additionally, Osiris has enhanced its mesenchymal stem
cell (MSC) patent estate with the issuance of patents across Europe and
Australia covering stem cells expressing all therapeutically useful
levels of cell surface receptors for TNF-alpha, a receptor essential to
the cell's ability to counteract inflammation. These patents further
support Osiris' considerable intellectual property position, which
includes 48 issued U.S. patents around the production, composition,
testing and use of the mesenchymal stem cell from both allogeneic and
autologous sources.
"These recent additions to Osiris' patent estate, combined with the
existing broad coverage of our pioneering MSC platform technology,
reinforce our industry leading IP portfolio and bolster our dominant
position regarding the manufacture and use of mesenchymal stem cells for
the treatment of a broad range of diseases," said Chris Alder, Chief
Intellectual Property Counsel of Osiris. "We have invested significant
time and resources building our intellectual property estate, and with
the commercialization of Prochymal, we are preparing to take the
necessary action to enforce our considerable rights."
Prochymal is now approved in Canada and New Zealand, and is currently
available in seven other countries including the United States under an
Expanded Access Program. With Prochymal (remestemcel-L) entering
commerce, Osiris has initiated the process of identifying entities that
may be infringing upon its intellectual property rights and will take
appropriate action as necessary.
About Prochymal (remestemcel-L)
Prochymal is the world's first approved drug with a stem cell as its
active ingredient. Developed by Osiris Therapeutics, Prochymal is an
intravenous formulation of MSCs, which are derived from the bone marrow
of healthy adult donors between the ages of 18 and 30 years. The MSCs
are selected from the bone marrow and grown in culture so that up to
10,000 doses of Prochymal can be produced from a single donor. Prochymal
is truly an off-the-shelf stem cell product that is stored frozen at the
point-of-care and infused through a simple intravenous line without the
need to type or immunosuppress the recipient. Prochymal is approved in
Canada and New Zealand for the management of acute graft-versus-host
disease (GvHD) in children and is available for adults and children in
eight countries including the United States, under an Expanded Access
Program. Prochymal is currently in a Phase 3 trial for refractory
Crohn's disease and is also being evaluated in clinical trials for the
treatment of myocardial infarction (heart attack) and type 1 diabetes.
About Osiris Therapeutics
Osiris Therapeutics, Inc. is the leading stem cell company, having
developed the world's first approved stem cell drug, Prochymal. The
company is focused on developing and marketing products to treat medical
conditions in inflammatory, cardiovascular, orthopedic and wound healing
markets. In Biosurgery, Osiris currently markets Grafix® for burns and
chronic wounds, and Ovation® for orthopedic applications. Osiris is a
fully integrated company with capabilities in research, development,
manufacturing and distribution of stem cell products. Osiris has
developed an extensive intellectual property portfolio to protect the
company's technology, including 48 U.S. and 144 foreign patents.
Osiris, Prochymal, Grafix and Ovation are registered trademarks of
Osiris Therapeutics, Inc. More information can be found on the company's
website, www.Osiris.com.
(OSIR‐G)
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development; status of the regulatory process for our biologic drug
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 Prochymal, Chondrogen and our other MSC and biologic drug
candidates; our cash needs; patents and proprietary rights; the safety
and ability of our potential products to treat disease and the results
of our scientific research; our plans for sales and marketing; our plans
regarding our facilities; types of regulatory frameworks we expect will
be applicable to our potential products; and results of our scientific
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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.

Osiris Therapeutics, Inc.
Erica Elchin, 443-545-1834
OsirisPR@Osiris.com
Source: Osiris Therapeutics, Inc.
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