Zomedica Corp. (NYSE American: ZOM) (“Zomedica” or the
“Company”), a veterinary health company creating point-of-care
diagnostics products for dogs and cats, today reported consolidated
financial results for the three and six months ended June 30, 2021.
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”).
Robert Cohen, Chief Executive Officer of
Zomedica stated that, “I fully understand and appreciate that what
all of our stakeholders, both internal and external, want to see is
continued execution on our goals and the building of increased
value in our business. For quite some time now, we have been
focused on executing on the many behind the scenes activities
necessary to advance and grow a young company. After a delay due,
in part, to the unexpected sale of our distribution partner and the
lack of completion of the fT4 and ACTH assays from our development
partner, we have implemented a new plan to place TRUFORMA®
Instruments in veterinary clinics. That program -- named our
Customer Appreciation Program -- provides interested customers with
a TRUFORMA® Instrument pursuant to a written agreement under which
the customer agrees to purchase assay cartridges for use on that
Instrument. Our intent not only is to sell cartridges to be used on
these Instruments, but also to establish an installed base of
TRUFORMA® Instruments so that assays available in the future can be
added to their then-existing usage, similar to a razor/razor blade
model. From July 13th, when we began the program, to yesterday, we
have secured 41 signed Instrument placement agreements and have
installed 25 TRUFORMA® Instruments under our Customer Appreciation
Program. These installations tend to lag approximately one to two
weeks behind the signature of an agreement. We are likely to
continue the Customer Appreciation Program until the availability
of the fT4 assay.”
Mr. Cohen continued, “Our business development
efforts also are continuing. We have evaluated many opportunities,
and intend to carefully evaluate all opportunities that we or
others bring to Zomedica. Potential structures of interest to the
Company range from acquisition to distribution of third-party
products to minority investment to securing the rights to
developing technologies, all with the intended goal of enhancing
the value of Zomedica by providing additional high-quality products
to our direct sales organization and additional value to both our
installed base of customers and new customers. With the continued
growth in the animal health market, we believe that now is an
opportune time to expand our product offerings in this exciting
industry.”
“To support TRUFORMA®, our sales organization
now has grown to include 10 Regional Diagnostic Specialists and
Territory Diagnostic Specialists, 3 Professional Services
Veterinarians, and 2 Inside Sales Representatives, all supported by
a Customer Service Department and managed by our Chief Commercial
Officer, Vice President of Sales, and two Area Sales Directors. We
continue to recruit additional members of the sales organization
and expect to have our sales and support teams at full planned
strength by the end of the Fall. We believe that this team is
capable of supporting not only TRUFORMA®, but also any additional
products that are added to Zomedica.”
Summary Second Quarter 2021
Results
Zomedica reported a net loss for the three and
six months ended June 30, 2021 of approximately $4.7 million, or
$.005 per share, and approximately $8.7 million, or $0.01 per
share, respectively, compared to a net loss of approximately $5.3
million, or $0.02 per share, for the three months ended June 30,
2020, an increase in income of approximately $0.6 million, or 11%
and a net loss of approximately $7.8 million, or $0.05 per share
for the six months ended June 30, 2020, a decrease in income of
approximately $0.9 million, or 13%.
Revenue for the three and six months ended June
30, 2021 was $15,693 and $29,817, respectively, and resulted from
the sale of our TRUFORMA® products and associated warranties. We
commenced commercialization of TRUFORMA® on March 15, 2021 and,
accordingly, had only limited sales activity in the first and
second quarters of 2021.
The Company believes that market acceptance of
TRUFORMA® has been adversely impacted by delays in the development
of our fT4 and ACTH assays by our development partner. We expect
that market adoption of TRUFORMA® will be challenging until our fT4
and ACTH assays are available for commercial release. We expect
that the fT4 assay will be available for commercial sale in the
fall of 2021 and that the ACTH assay will be available for
commercial sale by the end of 2021.
Cost of revenue for the three and six months
ended June 30, 2021 was $35,876 and $41,533, respectively. As noted
above, commercialization of TRUFORMA® commenced on March 15, 2021.
The Company expects that cost of revenue will increase as we sell
additional products in subsequent periods.
Research and development expense for the three
and six months ended June 30, 2021 was approximately $0.3 million
and approximately $0.7 million, respectively, compared to
approximately $3.9 million and $4.5 million for the three and six
months ended June 30, 2020, respectively, representing a decrease
of approximately $3.6 million, or 93%, over the prior three-month
period and a decrease of approximately $3.1 million, or 85%, for
the prior six-month period. The decrease in both periods was a
result of an overall reduction in research and development activity
as the Company curtailed our drug development activities, and a
reduction in development costs related to TRUFORMA® as the Company
completed development of the instrument and three of the first five
assays and began transitioning to commercialization activities.
Selling, general and administrative expense for
the three months ended June 30, 2021 was approximately $5.0
million, compared to approximately $1.4 million for the three
months ended June 30, 2020, an increase of approximately $3.6
million, or 261%. The increase primarily was due to an increase in
share-based compensation expense which was approximately $1.7
million for the three months ended June 30, 2021, compared to
approximately $0.1 million for the comparable period in 2020. Other
significant increases include regulatory fees incurred for the
annual shareholders meeting of approximately $0.9 million, salaries
of approximately $0.6 million, professional fees of approximately
$0.3 million, contracted expenditures of approximately $0.1
million, and marketing, travel and office expense of $0.1
million.
Liquidity and Outstanding Share
Capital
Zomedica had cash and cash equivalents of
approximately $276.2 million as of June 30, 2021, compared to
approximately $29.1 million as of June 30, 2020. The increase in
cash during the three months ended June 30, 2021 is mainly a result
of the cash flows from financing activities, partially offset by
cash flows used in operating and investing activities as discussed
below.
As of June 30, 2021, Zomedica had shareholders’
equity of approximately $276.1 million. After giving effect to
exercises of warrants and stock option exercises in July 2021, as
of August 11, 2021, Zomedica’s pro forma shareholders’ equity as of
June 30, 2021 would have been approximately $276.4 million.
Net cash used in operating activities for the
six months ended June 30, 2021 was approximately $4.4 million,
compared to approximately $7.9 million for the six months ended
June 30, 2020, a decrease of approximately $3.5 million, or 45%.
Approximately $3.0 million of current period expense is non-cash
expense associated with stock compensation, recorded as a result of
stock option grants in 2020, compared to the prior period of
approximately $0.3 million, approximately $0.5 million in gains
recognized on extinguishment of debt, and a loss on disposal of
property of $0.2 million. Other non-cash activity included
amortization and depreciation of approximately $0.2 million.
Accounts payable increased by approximately $1.9 million, offset in
part by an increase in inventory purchases of approximately $0.8
million.
Net cash used in investing activities for the
six months ended June 30, 2021 was approximately $0.1 million,
compared to net cash provided of approximately $1.0 million for the
six months ended June 30, 2020, an increase in net cash used of
approximately $1.1 million, or 114%. The increase in net cash used
in investing activities was due to the receipt of cash from the
modification of our lease in the first half of 2020 compared to
investments of intangible and other property and equipment in the
current period.
Net cash from financing activities for the six
months ended June 30, 2021 was approximately $218.7 million,
compared to approximately $35.5 million for the six months ended
June 30, 2020, an increase of approximately $183.2 million, or
517%. The increase resulted primarily from the sale of our equity
securities for total gross proceeds of approximately $199.5
million, cash received of approximately $32.1 million from warrant
exercises, and cash received of approximately $1.4 million from
stock option exercises, offset by stock issuance costs of
approximately $14.3 million.
As of June 30, 2021, Zomedica had an unlimited
number of authorized common shares with 977,950,993 common shares
issued and outstanding. As of August 11, 2021, Zomedica had
979,728,168 common shares issued and outstanding.
For complete financial results, please see
Zomedica’s filings on EDGAR and SEDAR or visit the Zomedica website
at www.ZOMEDICA.com.
For additional information regarding TRUFORMA®,
please click on the TRUFORMA® tab at the top of the home page on
the Zomedica website (www.zomedica.com).
About ZomedicaBased in Ann
Arbor, Michigan, Zomedica (NYSE American: ZOM) is a veterinary
health company creating products for dogs and cats by focusing on
the unmet needs of clinical veterinarians. Zomedica’s product
portfolio will include innovative diagnostics and medical devices
that emphasize patient health and practice health. It is Zomedica’s
mission to provide veterinarians the opportunity to increase
productivity and grow revenue while better serving the animals in
their care. For more information, visit www.ZOMEDICA.com.
Follow Zomedica
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Reader AdvisoryExcept for
statements of historical fact, this news release contains certain
"forward-looking information" or “forward-looking statements”
(collectively, “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 and include statements relating to our
expectations regarding future results. 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, including assumptions with respect to American economic
growth, demand for the Company’s products, the Company’s ability to
produce and sell its products, sufficiency of our budgeted capital
and operating expenditures, the satisfaction by our strategic
partners of their obligations under our commercial agreements, our
ability to realize upon our business plans and cost control efforts
and the impact of COVID-19 on our business, results and financial
condition.
Our forward-looking information is 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; uncertainty as
to the timing and results of development work and verification and
validation studies; uncertainty as to the timing and results of
commercialization efforts, as well as the cost of commercialization
efforts, including the cost to develop an internal sales force and
manage our growth; uncertainty as to our ability to supply
equipment and assays in response to customer demand; uncertainty as
to the likelihood and timing of any required regulatory approvals,
and the availability and cost of capital; the ability to identify
and develop and achieve commercial success for new products and
technologies; veterinary acceptance of our products; competition
from related products; 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; performance by our
strategic partners of their obligations under our commercial
agreements, including product manufacturing obligations; risks
pertaining to permits and licensing, intellectual property
infringement risks, risks relating to any required clinical trials
and regulatory approvals, risks relating to the safety and efficacy
of our products, the use of our products, intellectual property
protection, risks related to the COVID-19 pandemic and its impact
upon our business operations generally, including our ability to
develop and commercialize our products, and the other risk factors
disclosed in our filings with the SEC 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 Contact: PCG Advisory Kirin
Smith, Presidentksmith@pcgadvisory.com+1 646.823.8656
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