Hemostemix Inc. (“
Hemostemix” or the
“
Company”) (TSX VENTURE: HEM; OTC: HMTXF) is
pleased to announce the appointment of David Wood to the position
of Chairman, Bryson Goodwin to the position of Chief Executive
Officer, Thomas Smeenk to the position of President, and Natasha
Sever to the position of Chief Financial Officer. Yari Nieken will
replace Angus Jenkins, who recently resigned from the Company. Mr.
Nieken is an independent director. The Directors appointed the
Audit Committee and the Compensation Committee.
Mr. Wood is an independent director of the
Company and has a wide range of public company experience.
Most recently Mr. Wood sat on the board of directors from 1997
until the completion of its change of business transaction in
October 2019 of Black Bull Resources Inc., a former mining company,
which is now listed on the TSXV under the name Magnetic North
Acquisitions Corp. From 1999 to 2013, Mr. Wood served as a director
of Iplayco Corporation Ltd., a playground equipment designing and
manufacturing company, for which he also served as Chairman of the
Board from 2008 until 2011. Mr. Wood was a director and former CEO
and CFO of DataMiners Capital Corp., a NEX listed company, which
completed the reverse take of ZoomD Ltd. in August 2019.
Mr. Goodwin is a practiced international
executive with extensive experience in finance, management,
investor relations and operations with both private and public
companies. Bryson’s experience has demonstrated an operational,
market and banking track record in the technology, biotechnology
and resource sectors. Over the course of Mr. Goodwin’s career, he
has fostered an extensive high profile international association of
contacts and close relationships through networking and proficient
communication skills building performance driven teams.
Mr. Smeenk was the Founder, a Director,
President and Vice-President, Business Development for TheraVitae
Inc., which was taken over by Hemostemix Inc. as its Qualifying
Transaction. Mr. Smeenk is a project finance and business
development executive with a proven track record of bringing new
discoveries to market. He has been a public company executive since
1996, serving most recently as President & CEO of Broadway Gold
Mining Ltd, where he completed a $30 million agreement with Rio
Tinto. He served as Vice-President Business Development for Memex
Inc., a company he took public, President & CEO of
e-Manufacturing Networks Inc., President and CEO of Tyranex Gold
Inc. and President and CEO of IBI Corporation, where he made a
world class vermiculite discovery, which was subsequently sold to
Rio Tinto for $2,000,000.
Ms. Sever is a CPA designated in both Canada and
Australia with a BCom from Edith Cowan University. She joins the
Company with more than 10 years experience in senior finance roles
over a wide range of industries including mining, retail and
technology. Ms. Sever has held officer positions at a number of
publicly listed companies in both Canada and Australia and has a
proven record of working in alignment with, and to the benefit of
the Board and associated stakeholders. Her extensive experience
with company financings as well as TSX & ASX regulatory
compliance will serve to ensure the Company manages its affairs in
a transparent and proper fashion.
Mr. Nieken has a wide range of public
company and capital market experience. He founded Foremost Capital
Inc., an exempt market dealer and continues to consult for numerous
issuers in the healthcare, mineral extraction
and wellness sectors. He has served on the boards of several
public and private issuers and has raised substantial capital in
his career. He was formerly an investment adviser at Union
Securities Corp. Mr. Nieken holds an MBA from the Sydney
Graduate School of Management and a BA from the University of
British Columbia.
The Company announces it has rescinded the
Amended and Restated License Agreement granted to Aspire
Health Science, LLC (“Aspire”) dated September 30, 2019, primarily
due to Aspire’s failure to meet the Condition Precedent of paying
USD$1,000,000 within 30 business days of September 30, 2019, as
noted in the Company's Subsequent Events Note as prepared by
previous management for the period ended September 30, 2019. No
funds were received by the Company. The notice of rescission
was dated, emailed and couriered to Aspire on December 5,
2019.
Under the terms of Amended and Restated License
Agreement of September 30, 2019, if Hemostemix rescinds the
Agreement, Hemostemix and Aspire are released and discharged from
all obligations of the agreement, except the obligation of
confidentiality. The prior agreement, the License Agreement dated
February 15, 2018, is continued following Rescission, providing
Aspire with a limited license to ACP-01 for Approved Medical
Indications in a defined Territory. Under the terms of the February
15, 2018 License Agreement, the approved medical indications and
the territory are defined as follows: "Approved Medical Indications
mean Coronary Artery Disease (CAD), Peripheral Arterial Disease
(PAD), Critical Limb Ischemia (CLI). The Territory means the State
of Florida, as well as the Commonwealth of The Bahamas, the
Republic of Costa Rica, The Dominican Republic, the United Mexican
States and the Republic of Panama."
The Company would like to clarify that previous
management allowed the Contract Manufacturing Services Agreement
between it and Aspire dated February 15, 2018 to expire on July 31,
2019. The Company has notified Aspire that it intends to work
to mutual benefit on a month-to-month basis to complete the
clinical trial and negotiate in good faith to come to terms on a
new manufacturing agreement.
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 one of the first clinical-
stage biotech companies 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. 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.
Contact:
Bryson Goodwin or Thomas Smeenk,
Director, Hemostemix Inc.Suite 1150, 707 – 7th Avenue
S.W.Calgary, Alberta T2P 3H6BG: 604-341-1531 or TS:
905-580-4170
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 ability to fund operations, the Company’s
ability to negotiate a new manufacturing agreement to ensure
continued manufacturing for the Company’s Phase II clinical trial,
the Company’s stage of development, future clinical trials and
results, long-term capital requirements and 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. Additional
information identifying risks and uncertainties are contained in
the Company’s filing with the Canadian securities regulators, which
filings are available at www.sedar.com.
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