Dr. Gregory George MD PhD Joins Mesoblast Board
24 February 2025 - 10:33AM
Mesoblast Limited (Nasdaq:MESO; ASX:MSB), global leader in
allogeneic cellular medicines for inflammatory diseases, today
announced that it has appointed Dr. Gregory George MD PhD,
Mesoblast’s largest shareholder, to its Board of Directors.
Dr. George founded and managed the largest
privately owned ambulatory surgical center company in the United
States, SurgCenter Development. Dr. George brings to the Board his
background as a medical scientist with unique operational
experience having built a start-up company in the medical field and
turning it into a highly-efficient multi-billion-dollar commercial
organization.
Mesoblast Founder and Chief Executive Dr. Silviu
Itescu said, “Greg’s unique operational skills and insights will
provide tremendous value as Mesoblast transitions to become an
efficient commercial organization.”
Commenting on his appointment Dr. George said,
“I invested in Mesoblast because of my conviction in the
technology, Dr. Itescu’s scientific knowledge, vision, and
leadership combined with the ability of mesenchymal stem cells to
treat, and possibly cure, a wide array of disease processes. I
believe in Mesoblast’s potential to create a paradigm shift in
health care by blazing a new path forward and making the impossible
possible.”
Dr. George added, “I have first-hand knowledge
of how innovative treatments for musculoskeletal diseases such as
arthritis and back pain can transform patient outcomes and be
rapidly incorporated into commercial product offerings of
outpatient centers. While our Surgical Center company did not have
the advantage of having a unique product with a wide patent
portfolio like Mesoblast, we succeeded through operational
excellence, good communications, being proactive, and trying to
always beat timelines.”
Chair Jane Bell welcomed Dr. George to the Board
and said, “Greg brings not only a high conviction in Mesoblast and
our therapies but additionally important operational and strategic
dimensions to our Board that will facilitate our corporate goal of
building a major global commercial biotechnology company.”
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) 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 are expected to provide commercial
protection extending through to at least 2041 in 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
Twitter: @Mesoblast
Forward-Looking StatementsThis
press release includes forward-looking statements that relate to
future events or our future financial performance and involve known
and unknown risks, uncertainties and other factors that may cause
our actual results, levels of activity, performance or achievements
to differ materially from any future results, levels of activity,
performance or achievements expressed or implied by these
forward-looking statements. We make such forward-looking statements
pursuant to the safe harbor provisions of the Private Securities
Litigation Reform Act of 1995 and other federal securities laws.
Forward-looking statements should not be read as a guarantee of
future performance or results, and actual results may differ from
the results anticipated in these forward-looking statements, and
the differences may be material and adverse. Forward-looking
statements include, but are not limited to, statements about: the
initiation, timing, progress and results of Mesoblast’s preclinical
and clinical studies, and Mesoblast’s research and development
programs; Mesoblast’s ability to advance product candidates into,
enroll and successfully complete, clinical studies, including
multi-national clinical trials; Mesoblast’s ability to advance its
manufacturing capabilities; the timing or likelihood of regulatory
filings and approvals, manufacturing activities and product
marketing activities, if any; the commercialization of Mesoblast’s
RYONCIL for pediatric SR-aGVHD and any other product candidates, if
approved; regulatory or public perceptions and market acceptance
surrounding the use of stem-cell based therapies; the potential for
Mesoblast’s product candidates, if any are approved, to be
withdrawn from the market due to patient adverse events or deaths;
the potential benefits of strategic collaboration agreements and
Mesoblast’s ability to enter into and maintain established
strategic collaborations; Mesoblast’s ability to establish and
maintain intellectual property on its product candidates and
Mesoblast’s ability to successfully defend these in cases of
alleged infringement; the scope of protection Mesoblast is able to
establish and maintain for intellectual property rights covering
its product candidates and technology; estimates of Mesoblast’s
expenses, future revenues, capital requirements and its needs for
additional financing; Mesoblast’s financial performance;
developments relating to Mesoblast’s competitors and industry; and
the pricing and reimbursement of Mesoblast’s product candidates, if
approved. You should read this press release together with our risk
factors, in our most recently filed reports with the SEC or on our
website. Uncertainties and risks that may cause Mesoblast’s actual
results, performance or achievements to be materially different
from those which may be expressed or implied by such statements,
and accordingly, you should not place undue reliance on these
forward-looking statements. We do not undertake any obligations to
publicly update or revise any forward-looking statements, whether
as a result of new information, future developments or
otherwise.
Release authorized by the Chief Executive.
For more information, please contact:
Corporate Communications / Investors |
Media – Global |
Paul Hughes |
Allison Worldwide |
T: +61 3 9639 6036 |
Emma Neal |
E: investors@mesoblast.com |
T: +1 603 545 4843 |
|
E: emma.neal@allisonworldwide.com |
|
|
|
Media – Australia |
|
BlueDot Media |
|
Steve Dabkowski |
|
T: +61 419 880 486 |
|
E: steve@bluedot.net.au |
|
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