Imprimis Pharmaceuticals, Inc. (NASDAQ: IMMY) today reported
results for the third quarter 2018.
Third Quarter 2018 and Other Recent
Notable Highlights:
- Revenues increased 66% year-over-year to $10.7 million
- Ophthalmology revenue increased 81% year-over-year to $8.9
million
- Gross margin increased to 61% from 48% in the third quarter
2017
- Second consecutive quarter of positive adjusted EBITDA (a
non-GAAP measure) of $424,000
- Cash balance increased for the second consecutive quarter
- Terminated At-the-Market (ATM) equity sales agreement due to
positive operating position
- Eton Pharmaceuticals, former Imprimis subsidiary, completes
upsized IPO; now trading on NASDAQ under the symbol “ETON”
- Melt Pharmaceuticals subsidiary files Pre-IND meeting request
with FDA; starts two preparatory drug development investigator led
studies
- Two new drug development subsidiaries, Mayfield Pharmaceuticals
and Radley Pharmaceuticals, formed and seeded with drug
formulations intended to be taken through FDA’s 505(b)(2)
development pathway
- Board of Directors approved plan to change corporate name to
Harrow Health, Inc. pending shareholder approval
Mark L. Baum, CEO of Imprimis, commented,
“Despite nearly $600,000 in one-time investments for costs incurred
by our subsidiary Melt Pharmaceuticals, Inc. and litigation, we
continued to deliver positive adjusted earnings. This quarter
showed strong performance, including record revenues and gross
margins, increasing cash balances and an outlook of continued
revenue growth from our core operating business. Importantly,
now that we are past the typically weak third calendar quarter, we
are seeing our positive momentum continue into the fourth quarter
in several critical ways we will comment on during our conference
call.”
Baum added, “We’re in the best operational place
we’ve been in since the founding of the company in 2011. The
initial public offering (IPO) of our former subsidiary, Eton
Pharmaceuticals, which now trades on NASDAQ, is only the beginning
of what we intend to achieve. Shareholders have embraced our
diversification strategy – to build, own and generate potential
cash flow through royalties from a diversified portfolio of
healthcare businesses. With the success of our operating
business, the IPO of Eton, and the key milestones we expect our
second spin-out and former subsidiary, Surface Pharmaceuticals, to
reach next year, we are optimistic about the potential of our other
three subsidiaries, including Melt Pharmaceuticals, and two new
businesses formed during the third and fourth quarter, Mayfield
Pharmaceuticals and Radley Pharmaceuticals.”
Baum concluded, “To better reflect our direction
going forward, our Board of Directors has voted to change our
company name to Harrow Health, Inc. A harrow prepares the
ground for valuable crops to be planted, grow and create
yield. This concept is reflected in practice as we created
and produced a better than 230% compound annual growth rate (CAGR)
for our core operating business over the past four years, and at
the same time, created Eton, Surface, Melt, Mayfield and
Radley. Once our name change is approved by our shareholders,
everything we own and are developing will be a part of Harrow
Health.”
Conference Call and Webcast
The company’s management team will host a
conference call and audio-only webcast today at 4:30 p.m. EST (1:30
p.m. PST) to discuss the financial results and recent developments.
To participate in the call, please dial (877) 407-8031 for domestic
callers or (201) 689-8031 for international callers. To
listen to the webcast, please click here or visit the investor
relations section of the Imprimis website by clicking here. A
dial in replay of the call will be available until December 13,
2018. To access the replay, dial (877) 481-4010 domestically
or (919) 882-2331 internationally and reference Replay ID:
40047. The webcast replay will be available until February
13, 2019.
Financial Summary:
Selected highlights regarding operating results
for the three months and nine months ended September 30, 2018 and
for the same periods in 2017 are as follows (in thousands, except
per share data):
|
For the three months ended September 30,
2018 |
For the three months ended September 30,
2017 |
Total Revenues |
$ 10,739 |
|
$ 6,483 |
|
Cost of Sales |
|
(4,191 |
) |
|
(3,403 |
) |
Gross Profit |
|
6,548 |
|
|
3,080 |
|
Selling, General & Administrative Expenses |
|
(6,964 |
) |
|
(5,781 |
) |
Research & Development Expenses |
|
(233 |
) |
|
(63 |
) |
Operating Loss |
|
(649 |
) |
|
(2,764 |
) |
Other Expense, net |
|
(1,865 |
) |
|
(2,928 |
) |
Net Loss |
$ (2,514 |
) |
$
(5,692 |
) |
Net Loss per Common Share, Basic and Diluted |
$ (0.12 |
) |
$ (0.28 |
) |
|
For the nine months ended
September 30, 2018 |
For the nine months ended
September 30, 2017 |
Total Revenues |
$ 29,988 |
|
$ 19,437 |
|
Cost of Sales |
|
(12,419 |
) |
|
(10,048 |
) |
Gross Profit |
|
17,569 |
|
|
9,389 |
|
Selling, General & Administrative Expenses |
|
(20,231 |
) |
|
(19,077 |
) |
Research & Development Expenses |
|
(392 |
) |
|
(324 |
) |
Operating Loss |
|
(3,054 |
) |
|
(10,012 |
) |
Other Income (Expense), net |
|
(451 |
) |
|
798 |
|
Net Loss |
$ (3,505 |
) |
$
(9,214 |
) |
Net Loss per Common Share, Basic and Diluted |
$ (0.16 |
) |
$ (0.47 |
) |
Adjusted EBITDA
In addition to the company's results of
operations determined in accordance with U.S. generally accepted
accounting principles (GAAP), which are presented and discussed
above, management also utilizes adjusted EBITDA, an unaudited
financial measure that is not calculated in accordance with GAAP,
to evaluate the company's financial results and performance and to
plan and forecast future periods. Adjusted EBITDA is considered a
"non-GAAP" financial measure within the meaning of Regulation G
promulgated by the SEC. Management believes that this
non-GAAP financial measure reflects an additional way of viewing
aspects of the company's operations that, when viewed with GAAP
results, provides a more complete understanding of the company's
results of operations and the factors and trends affecting its
business. Management believes adjusted EBITDA provides
meaningful supplemental information regarding the company's
performance because (i) it allows for greater transparency
with respect to key metrics used by management in its financial and
operational decision-making; (ii) it excludes the impact of
non-cash or, when specified, non-recurring items that are not
directly attributable to the company's core operating performance
and that may obscure trends in the company's core operating
performance; and (iii) it is used by institutional investors
and the analyst community to help analyze the company's
results. However, adjusted EBITDA and any other non-GAAP
financial measures should be considered as a supplement to, and not
as a substitute for, or superior to, the corresponding measures
calculated in accordance with GAAP. Further, non-GAAP financial
measures used by the company and the manner in which they are
calculated may differ from the non-GAAP financial measures or the
calculations of the same non-GAAP financial measures used by other
companies, including the company's competitors.
The company defines adjusted EBITDA as net
income (loss) excluding the effects of interest, taxes,
depreciation, amortization, stock-based compensation, other income
(expense) and, if any and when specified, other non-recurring
income or expense items. The company believes that the most
directly comparable GAAP financial measure to adjusted EBITDA is
net loss. Adjusted EBITDA has limitations and should not be
considered as an alternative to gross profit or net loss as a
measure of operating performance or to net cash provided by (used
in) operating, investing or financing activities as a measure of
ability to meet cash needs.
The following is a reconciliation of adjusted
EBITDA, a non-GAAP measure to the most comparable GAAP measure, net
loss, for the three months ended September 30, 2018 and for the
same period in 2017 (in thousands):
|
For the three months ended
September 30, 2018 |
For the three months ended
September 30, 2017 |
GAAP Net Loss |
$ (2,514 |
) |
$ (5,692 |
) |
Stock-based compensation and payments |
|
591 |
|
|
648 |
|
Interest expense, net |
|
705 |
|
|
793 |
|
Taxes |
|
- |
|
|
(28 |
) |
Depreciation |
|
423 |
|
|
382 |
|
Amortization of intangible assets |
|
59 |
|
|
91 |
|
Early extinguishment of debt |
|
- |
|
|
884 |
|
Investment loss from Surface and Eton |
|
1,160 |
|
|
1,237 |
|
Other Expense, net |
|
- |
|
|
42 |
|
Adjusted E(L)BITDA |
$ 424 |
|
$ (1,643 |
) |
About Imprimis Pharmaceuticals
Imprimis Pharmaceuticals, Inc. (NASDAQ: IMMY)
owns a diversified portfolio of healthcare businesses, including
the nation’s leading ophthalmology pharmaceutical compounding
business, ImprimisRx. The company also holds large equity
positions in Eton Pharmaceuticals (NASDAQ: ETON), Surface
Pharmaceuticals, Melt Pharmaceuticals, Mayfield Pharmaceuticals and
Radley Pharmaceuticals, companies founded as subsidiaries of
Imprimis. The Company also owns royalty rights in certain
505(b)(2) drug candidates being developed by Eton, Surface, Melt,
Mayfield and Radley. For more information about Imprimis,
please visit the Investor Relations section of the corporate
website by clicking here.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of the U.S. Private Securities
Litigation Reform Act of 1995. Any statements in this release that
are not historical facts may be considered such "forward-looking
statements." Forward-looking statements are based on management's
current expectations and are subject to risks and uncertainties
which may cause results to differ materially and adversely from the
statements contained herein. Some of the potential risks and
uncertainties that could cause actual results to differ from those
predicted include our ability to make commercially available our
compounded formulations and technologies in a timely manner or at
all; physician interest in prescribing our formulations; risks
related to our compounding pharmacy operations; our ability to
enter into other strategic alliances, including arrangements with
pharmacies, physicians and healthcare organizations for the
development and distribution of our formulations; our ability to
obtain intellectual property protection for our assets; our ability
to accurately estimate our expenses and cash burn, and raise
additional funds when necessary; risks related to research and
development activities; the projected size of the potential market
for our technologies and formulations; unexpected new data, safety
and technical issues; regulatory and market developments impacting
compounding pharmacies, outsourcing facilities and the
pharmaceutical industry; competition; and market conditions. These
and additional risks and uncertainties are more fully described in
Imprimis' filings with the Securities and Exchange Commission,
including its Annual Report on Form 10-K and its Quarterly Reports
on Form 10-Q. Such documents may be read free of charge on the
SEC's web site at www.sec.gov. Undue reliance should not be placed
on forward-looking statements, which speak only as of the date they
are made. Except as required by law, Imprimis undertakes no
obligation to update any forward-looking statements to reflect new
information, events or circumstances after the date they are made,
or to reflect the occurrence of unanticipated events.
No Imprimis compounded formulation is
FDA-approved. Other than drugs compounded at a registered
outsourcing facility, all Imprimis compounded formulations require
a prescription for an individually identified patient consistent
with federal and state laws.
Investor ContactJon Patton
jpatton@imprimispharma.com
858.704.4587
Media ContactDeb HollidayHolliday
Communications, Inc.deb@hollidaycommunications.net412.877.4519
Source: Imprimis Pharmaceuticals, Inc.
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