Zomedica Pharmaceuticals Corp. (NYSE American:ZOM) (TSX-V:ZOM)
(“Zomedica” or “Company”), a veterinary diagnostic and
pharmaceutical company, today reported consolidated financial
results for the second quarter ended June 30, 2018. Amounts, unless
specified otherwise, are expressed in U.S. dollars and presented
under accounting principles generally accepted in the United States
of America (“U.S. GAAP”).
“Strategically, we have made significant progress in advancing
our product pipeline with the addition of our innovative
point-of-care diagnostic product, ZM-020,” said Gerald Solensky,
Jr., Chairman and CEO of Zomedica. “This new product, along with
others in our pipeline, are focused on bringing best-in-class
solutions to clinical veterinarians that increase practice
productivity and elevate the standard of care they provide to our
companion animals.”
Corporate Highlights
- On May 10, 2018 Zomedica announced it entered into a
development, commercialization and exclusive distribution agreement
with Seraph Biosciences, Inc. to develop and market a novel
pathogen detection system in the form of an innovative
point-of-care diagnostic instrument, referred to as ZM-020.
- On June 19, 2018 Zomedica provided a product development update
and expected milestones of the diagnostics, ZM-017 and ZM-020, and
the therapeutics, ZM-007, ZM-012, ZM-006 and ZM-011.
- On June 25, 2018 Zomedica announced it joined the Russell 3000™
Index and the Russell Microcap® Index at the conclusion of the
Russell US Indexes annual reconstitution.
- On June 28, 2018 Zomedica announced that it had sold an
aggregate of 1,861,627 common shares at a price of $2.15 per share
in a private offering for aggregate gross proceeds of
$4,002,496.
Summary Second Quarter 2018 ResultsZomedica
recorded net loss and comprehensive loss for the three and six
months ended June 30, 2018 of $4,144,398 or $0.04 per share and
$6,315,727 or $0.07 per share, compared to a loss of $1,588,370 or
$0.02 per share and $3,421,106 or $0.04 per share for the three and
six months ended June 30, 2017.
Zomedica, which is in the development stage, recorded no
revenues in the three and six months ended June 30, 2018. For the
three and six months ended June 30, 2018, net loss resulted from
research and development (“R&D”) expenses of $2,534,620 and
$3,134,961, general and administrative (“G&A”) expenses of
$1,248,490 and $2,408,662, and professional fees of $336,455 and
$708,402. For the three and six months ended June 30, 2017, the net
loss was attributed to G&A expenses of $748,610 and $1,575,635,
R&D expenses of $504,235 and $1,120,684 and professional fees
of $314,658 and $696,194.
Expenditures for R&D for the three and six months ended June
30, 2018 were $2,534,620 and $3,134,961 compared to $504,235 and
$1,120,684 for the three and six months ended June 30, 2017. The
increases were primarily due to the up-front licensing fee related
to the signing of a development, commercialization and exclusive
distribution agreement with Seraph Biosciences, Inc. of $1,738,513,
and accrued payments to Seraph for previously incurred development
costs of $333,247 included in contracted expenditures. The up-front
licensing fee represented the issuance of unregistered common
shares having a value of $1,238,513 and a cash payment of $500,000.
Other significant expenditures include contracted expenditures of
$438,689 and $708,212, and salaries of $174,067 and $326,439 for
the three and six months ended June 30, 2018. However, there was
also a reduction in salaries, bonuses and benefits as we did not
have a Chief Medical Officer in the three and six months ended June
30, 2018. Overall there was an increased level of lab activities,
including in vitro and in vivo work, to support the further
development of our product candidates ZM-017, ZM-020, ZM-007,
ZM-012, ZM-006 and ZM-011. We expect that our R&D expenditures
in 2018 will be significantly higher than in 2017, due to the
upfront and milestone payments of licensed technologies, initiation
of pilot and pivotal studies related to our four investigational
new animal drug applications, work related to verification and
validation of ZM-020 and ZM-017, and additional veterinary
pharmaceutical candidates, diagnostic developments and
technologies.
G&A expenses for the three and six months ended June 30,
2018 were $1,248,490 and $2,408,662 compared to $748,610 and
$1,575,635 for the three and six months ended June 30, 2017. The
increases were primarily due to significant expenses related to the
addition of personnel, accounting for salaries of $859,268 and
$1,502,555. Increases to salaries in the three and six months ended
June 30, 2018 include the addition of a Chief Commercial Officer, a
Vice President of Sales and accrued severance to a former officer
of the Company. Other expenses for the three and six months ended
June 30, 2018 included regulatory expense of $90,142 and $193,700,
travel and accommodation of $70,463 and $191,868, insurance costs
of $77,282 and $157,743, and office expenses of $61,460 and
$138,406. We expect that general and administrative expense will
increase in 2018 and future periods as we increase our level of
activity.
Professional fees for the three and six months ended June 30,
2018 were $336,455 and $708,402 compared to $314,658 and $696,194
for the three and six months ended June 30, 2017. Professional fees
for the 2018 period consisted primarily of consulting fees incurred
in connection with preparation and completion of additional SEC
filings and updates, and costs incurred in being a public company
across two jurisdictions, Canada and U.S.
Liquidity and Outstanding Share CapitalZomedica
had cash and cash equivalents of $4,279,163 as of June 30, 2018,
compared to $3,448,147 as of December 31, 2017. The increase in
cash during the six months ended June 30, 2018 is mainly a result
of the cash flows provided by financing activities, partially
offset by cash flows used in operating activities as discussed
below.
For the three and six months ended June 30, 2018, cash flows
used in operating activities amounted to $2,740,495 and $4,448,289.
The largest uses of cash stemmed from an increase in salaries,
bonus and benefits as we had 20 employees at June 30, 2018,
compared to 18 employees at June 30, 2017. Other significant
increases in uses of cash include the Seraph up-front licensing fee
cash payment of $500,000, increased regulatory and insurance
expenses related to our listing on the NYSE American, and increased
travel and accommodation expenses related to business development
and pre-marketing activities.
For the three and six months ended June 30, 2018 the cash flows
from financing activities relate to cash proceeds from financing of
$4,002,496 and the exercise of stock options of $30,522 for the
three months ended and $1,438,308 for the six months ended June 30,
2018.
As of June 30, 2018, Zomedica had an unlimited number of
authorized common shares with 94,511,209 common shares issued and
outstanding. As of August 9, 2018, Zomedica had 94,511,209 common
shares issued and outstanding.
As of June 30, 2018 and December 31, 2017, Zomedica had
shareholders’ equity of $4,734,157 and $4,387,085,
respectively.
For complete financial results, please see Zomedica’s filings on
EDGAR and SEDAR or visit the Zomedica website at
www.ZOMEDICA.com.
About ZomedicaBased in Ann Arbor, Michigan,
Zomedica (NYSE American:ZOM) (TSX-V:ZOM) is a veterinary diagnostic
and pharmaceutical company creating products for companion animals
(canine, feline and equine) by focusing on the unmet needs of
clinical veterinarians. Zomedica’s product portfolio includes novel
diagnostics and innovative therapeutics that emphasize patient
health and practice health. With a team that includes clinical
veterinary professionals, it is Zomedica’s mission to give
veterinarians the opportunity to lower costs, increase
productivity, and grow revenue while better serving the animals in
their care. For more information, visit www.ZOMEDICA.com.
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Reader AdvisoryNeither TSX Venture Exchange nor
its Regulation Services Provider (as that term is defined in the
policies of the TSX Venture Exchange) accepts responsibility for
the adequacy or accuracy of the release.
Except for statements of historical fact, this news release
contains certain "forward-looking information" within the meaning
of applicable securities law. Forward-looking information is
frequently characterized by words such as "plan", "expect",
"project", "intend", "believe", "anticipate", "estimate" and other
similar words, or statements that certain events or conditions
"may" or "will" occur. Although we believe that the expectations
reflected in the forward-looking information are reasonable, there
can be no assurance that such expectations will prove to be
correct. We cannot guarantee future results, performance or
achievements. Consequently, there is no representation that the
actual results achieved will be the same, in whole or in part, as
those set out in the forward-looking information.
Forward-looking information is based on the opinions and
estimates of management at the date the statements are made, and
are subject to a variety of risks and uncertainties and other
factors that could cause actual events or results to differ
materially from those anticipated in the forward-looking
information. Some of the risks and other factors that could cause
the results to differ materially from those expressed in the
forward-looking information include, but are not limited to:
uncertainty as to whether our strategies and business plans will
yield the expected benefits; availability and cost of capital; the
ability to identify and develop and achieve commercial success for
new products and technologies; the level of expenditures necessary
to maintain and improve the quality of products and services;
changes in technology and changes in laws and regulations; our
ability to secure and maintain strategic relationships; risks
pertaining to permits and licensing, intellectual property
infringement risks, risks relating to future clinical trials,
regulatory approvals, safety and efficacy of our products, the use
of our product, intellectual property protection and the other risk
factors disclosed in our filings with the Securities and Exchange
Commission and under our profile on SEDAR at www.sedar.com. Readers
are cautioned that this list of risk factors should not be
construed as exhaustive.
The forward-looking information contained in this news release
is expressly qualified by this cautionary statement. We undertake
no duty to update any of the forward-looking information to conform
such information to actual results or to changes in our
expectations except as otherwise required by applicable securities
legislation. Readers are cautioned not to place undue reliance on
forward-looking information.
Investor Relations ContactsShameze Rampertab,
CPA, CAsrampertab@zomedica.com+1 647.283.3630
PCG Advisory GroupKirin Smith, COOksmith@pcgadvisory.com+1
646.863.6519www.pcgadvisory.com
Media ContactAndrea
Eberleaeberle@zomedica.com+1 734.369.2555
Zomedica Pharmaceuticals (TSXV:ZOM)
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