CALGARY, Alberta, July 05, 2018 (GLOBE NEWSWIRE) -- Hemostemix Inc. (“Hemostemix” or the
“Company”) (TSX-V:HEM) is pleased to announce the formalization of its Scientific Advisory Board
(“SAB”). Members of the SAB are all leaders in their fields of expertise, which span biochemistry, molecular biology,
genomics and medicine. The mandate of the Scientific Advisory Board will be to serve as a strategic resource for Hemostemix
to advise on research and development initiatives surrounding its stem cell technology product pipeline and the furtherance of
Hemostemix’s clinical pipeline and support the Company’s overall mission. Members of the SAB are:
Dr. Alan Lumsden, M.D.
Dr. Alan B. Lumsden, M.D., is the Walter W. Fondren III Chair, Medical Director of the Houston Methodist DeBakey
Heart & Vascular Center and chair of the Department of Cardiovascular Surgery at Houston Methodist Hospital. He received his
Bachelor of Medicine and Surgery at the University of Edinburgh where he graduated at the top of his class. After completing
a year-long internship, he moved to Emory University in Atlanta where he completed his surgical residency and vascular training and
eventually became the Chief of the Division of Vascular Surgery. In 2002, he joined Michael E. DeBakey Department of Surgery
at Baylor College of Medicine as Professor and Chief of the Division of Vascular Surgery and Endovascular Therapy. He assumed
his positions at Houston Methodist Hospital in 2008.
Dr. Lumsden has developed an international reputation as a leader in the field of endovascular surgery. He
conducts FDA-mandated training for surgeons nationwide and has received significant funding for his research from the National
Institutes of Health. He has contributed more than 200 papers to medical literature.
Houston Methodist Hospital has been recognized by U.S. News & World Report as one of the top 20 hospitals in the
United States, placing it for the second time on the magazine’s prestigious Honor Roll. It is also designated as a Magnet
hospital for excellence in nursing.
Dr. Norman Wong, M.D.
Dr. Norman C. W. Wong, B.Sc (Hon), M.Sc, M.D., FRCP(C) is a Co-Founder of Resverlogix Corp. (TSX:RVX), and has
been its Chief Scientific Officer since 2003. Dr. Wong serves as Professor of Medicine and Biochemistry & Molecular Biology
as well as the Director of the Libin Gene/Cell Therapy Unit within the Faculty of Medicine at the University of Calgary. Dr.
Wong has been associated with the University of Calgary since 1987 and also has held the posts of Associate Vice-President of
Research and International and Assistant Dean (Research) Faculty of Medicine.
Dr. Wong specializes in the areas of: Endocrinology, Internal Medicine, Molecular Biology, and Gene/Cell
Therapy. His most recent successes have come from elucidating the potential therapeutic opportunities for cardiovascular
disease by examining the epigenetic mechanisms underlying this deadly disease. He has been the author and co-author of more
than 275 articles and abstracts and has been invited to sit on more than 40 national or international panels and committees.
He has also acted as a consultant to several leading pharmaceutical companies, including Eli Lilly, Merck Frost, GlaxoSmithKline,
Solvay Pharmaceuticals and Abbott Laboratories. Dr. Wong also previously served as a member of the SAB at Hemostemix.
Dr. Wong graduated with a Bachelor of Science degree with honors at the University of Calgary in 1975. He subsequently
obtained a Master of Science degree in Medical Biochemistry in 1977 and a Medical Degree in 1980, also from the University of
Calgary.
Dr. Kumar L. Hari, PhD
Dr. Hari’s expertise spans chromosome biology, functional genomics, and bioinformatics. Dr. Hari has been
the Chief Science Officer at cBio Corp. (“cBio”), a private company that provided infectious disease diagnostics and
tracking. At cBio, Dr. Hari led the team in engagements with the FDA, various universities and other US government
organization. Prior to working at cBio, he held business development and program management roles at Ibis Biosciences, Inc.,
and Abbott Molecular, Inc., where his work led directly to the spin-off of cBio. Dr. Hari has been a director of program
management efforts at the California Institute of Regenerative Medicine and at the Myelin Repair Foundation. Dr. Hari earned
his PhD in Cell Biology from UC San Diego and a B.Sc. in Genetics from UC Davis.
Dr. Hari provided due diligence support when evaluating Hemostemix’s science, therapeutic products and clinical
trials. He has already provided invaluable guidance and perspective on Hemostemix’s research and development efforts, as well
as clinical development programs.
Hemostemix’s Chief Scientific Officer, Dr. Ravi Jain, states, “It is a great pleasure to announce the
finalization and launch of our Scientific Advisory Board. We have been able to attract an excellent team of world-class
talent from scientific fields that support the development of our stem cell technology, including our newest member, Dr. Lumsden,
MD, whose appointment at the Houston Methodist hospital, one of the leading hospitals in the United States, ranks him as one of the
leading physicians in his field. We aim to utilize the profound knowledge of these individuals and their vast networks to
challenge, support and advise Hemostemix in order to keep us at the leading-edge of product research and development for stem cell
technologies.”
Going forward, the SAB will be tasked with providing strategic and scientific counsel in the development of
Hemostemix’s lead product, which is in North American Phase II Clinical Trial for critical limb ischemia (CLI), and Hemostemix’s
R&D pipeline. In addition, the SAB will guide the scientific vision for the improvement and development of other products
based on Hemostemix’s proprietary technology, including applications for cardiovascular, neurological and vascular indications.
ABOUT HEMOSTEMIX INC.
Hemostemix is a publicly traded clinical-stage biotechnology company that develops and commercializes innovative
blood-derived cell therapies for medical conditions not adequately addressed by current treatments. It is the first clinical-stage
biotech company to test a stem-cell therapy in an international, multicenter, Phase II clinical trial for patients with critical
limb ischemia (“CLI”), a severe form of peripheral artery disease (“PAD”) caused by reduced blood flow to the legs. The Phase II
trial targets a participant’s diseased tissue with proprietary cells grown from his or her blood that can support the formation of
new blood vessels. The Company’s intellectual property portfolio includes over 50 patents issued or pending throughout the
world. Hemostemix has a manufacturing contract with Aspire Health Science, LLP (“Aspire”), for the production of ACP-01 and
for research and development purposes at Aspire’s Orlando, Florida, facility. Building towards commercialization, Hemostemix
has also licensed the use, sale and import of ACP-01 for certain indications to Aspire in certain jurisdictions. The Company is
continuing research and development of its lead product, ACP-01 with other applications, including cardiovascular, neurological and
vascular indications.
For more information, please visit www.hemostemix.com or email office@hemostemix.com.
Contact:
Kyle Makofka, President and CEO
Suite 1049, 150 – 9th Avenue S.W.
Calgary, Alberta T2P 3H9
Phone: (403) 506-3373
E-Mail: kmakofka@hemostemix.com
Neither the TSX Venture Exchange nor its Regulation Service Provider (as that term is defined under
the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this
release.
Forward-Looking Statements
This release may contain forward-looking statements. Forward-looking statements are statements that are not
historical facts and are generally, but not always, identified by the words “expects,” “plans,” “anticipates,” “believes,”
“intends,” “estimates,” “projects,” “potential,” and similar expressions, or that events or conditions “will,” “would,”
“may,” “could,” or “should” occur. Although Hemostemix believes the expectations expressed in such forward-looking statements are
based on reasonable assumptions, such statements are not guarantees of future performance and actual results may differ materially
from those in forward-looking statements. Forward-looking statements are based on the beliefs, estimates, and opinions of
Hemostemix management on the date such statements were made. By their nature forward-looking statements are subject to known and
unknown risks, uncertainties, and other factors which may cause actual results, events or developments to be materially different
from any future results, events or developments expressed or implied by such forward-looking statements. Such factors include, but
are not limited to, the Company’s stage of development, future clinical trial results, long-term capital requirements and future
ability to fund operations, future developments in the Company’s markets and the markets in which it expects to compete, risks
associated with its strategic alliances and the impact of entering new markets on the Company’s operations. Each factor should be
considered carefully and readers are cautioned not to place undue reliance on such forward-looking statements. Hemostemix expressly
disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information,
future events, or otherwise.
