Hemostemix Announces Convertible Debenture Financing
15 Abril 2019 - 9:30AM
NOT FOR DISTRIBTUTION TO U.S. NEWS WIRE
SERVICES OR DISSEMINATION IN THE UNITED STATES
Hemostemix Inc. (“
Hemostemix” or the
“
Company”) (TSX VENTURE: HEM; OTCQB: HMTXF) a
biotechnology company focused on developing and commercializing
innovative blood-derived stem cell therapies for medical conditions
not adequately addressed by current treatments, is pleased to
announce that it intends to complete, subject to regulatory
approval, a non-brokered private placement of up to a maximum of
$6,000,000 principal amount of secured convertible debentures (the
“Offering”).
Each debenture will consist of $1,000 aggregate
principal amount of 8% secured, non-transferable, convertible,
redeemable debentures (the “Debentures”). The Debentures will
mature twenty four (24) months from the date of issuance (the
"Maturity Date”) and bear interest at a rate of 8% per annum. The
principal amount of the Debentures is convertible into common
shares of the Company (“Common Shares”) at the option of the
holder, at a price of $0.08 per Common Share in the first year
after the date of issuance and at a price of $0.10 in the second
year (as applicable, the “Conversion Price”), subject to TSX
Venture Exchange (“TSXV”) approval. The Company may elect to force
the conversion of the principal amount of the outstanding
Debentures at the Conversion Price (“Mandatory Conversion”), on not
more than 60 days’ and not less than 30 days’ notice, if the daily
closing trading price of the common shares on the TSXV is greater
than $0.20 for 20 consecutive trading days preceding such notice,
subject to the Mandatory Conversion being permitted under the
policies of the TSXV. The Debentures will be secured obligations of
the Company. The Debentures may be redeemed by the Company,
in whole or in part, plus any accrued and unpaid interest, at any
time prior to the Maturity Date. Finders’ fee may be payable
in conjunction with the Offering at the election of the
Company.
The Debentures, and any common shares issuable
upon conversion will be subject to a four month hold period from
the date of closing.
The proceeds of the Debenture Offering will be
used to continue to fund the Company’s phase II clinical trial for
critical limb ischemia (“CLI”), research and development, costs
towards other clinical trials including application for an angina
pectoris trial and for general working capital. Certain
insiders of the Company intend to subscribe for Debentures pursuant
to the Offering.
Kyle Makofka, Hemostemix’s CEO commented,
“Hemostemix has accomplished several important milestones recently
including the addition of a world class Chief Medical Officer and
achieving escalated trial enrollment for its CLI trial.
Completion of this financing should provide the Company with the
funds to reach interim analysis for its CLI trial as well as
initiate another clinical trial. The past eighteen months has seen
the Company fulfill several significant milestones and this
additional funding will provide the resources for the Company’s to
continue to further the potential of its lead product ACP-01.”
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. Hemostemix has a manufacturing contract with Aspire
Health Science, LLC (“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, CEO Suite 2150, 300 – 5th Avenue S.W. Calgary,
Alberta T2P 3C4Phone: (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, the ability of ACP-01 to qualify
for and be granted Orphan Drug Status, future clinical trials and
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.
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