Corgenix Medical Corporation (OTC BB: CONX.OB), a worldwide developer
and marketer of diagnostic test kits, today filed its fiscal quarter
Form 10-Q and reported financial results. The report disclosed that the
company achieved record operating results for the quarter ended
September 30, 2012.
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Revenue for the quarter increased 29.5% to a record $2.82 million from
$2.18 million in the same period of the prior year. Most of the growth
was in contract manufacturing (up 291%), liver disease (up 37%),
coagulation (up 32%) and AspirinWorks® (up 19%).
Geographically, North American revenues increased 30.4% and
international revenues increased 24.1%.
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Total gross profit for the quarter increased 14.8% to a record of
$1.20 million from $1.05 million in the previous year.
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Operating expenses declined from the first quarter in the prior year
by 4.2% while interest expense decreased 89.4% to $6,000 in the
current quarter from $60,000 in the prior year.
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Operating income increased to $205,000 in the first quarter of 2012
from $6,000 in the first quarter of 2011.
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The company achieved record net income for the current quarter of
$198,000 versus a net loss of $50,000 in the prior year, while EBITDA
increased 165% to $305,000.
Unaudited Financials at a Glance (in thousands, except percentages)
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Q1 2012
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Q1 2011
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Percent Change
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Revenue
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$2,821
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$2,178
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29.5%
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Gross Profit
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$1,202
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$1,047
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14.8%
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Operating Expenses
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$997
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$1,042
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(4.2%)
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Operating Income
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$205
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$6
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---
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Net Income (Loss)
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$198
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($50)
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---
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EBITDA
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$305
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$115
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165.0%
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“We had a solid first quarter and are very encouraged that our key
strategic initiatives are beginning to pay off in a more stable business
with solid profitability,” said Douglass Simpson, President and CEO of
Corgenix. “We’re continuing to take important steps to maintain this
growth in revenues and earnings to ensure long-term success, and we’re
confident that our focus on the most important growth areas will
continue to drive increased value for our shareholders.”
Business Development Highlights for the Quarter ended September 30,
2012
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Completed preliminary discussions with the U.S. Food and Drug
Administration (FDA) on several diagnostic products in advance of
510(k) submissions expected in Q3 and Q4
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Continued expansion of international business through the ELITech
Group, focusing on securing regulatory approval in key countries
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Advanced automated systems program with the installation and initial
sales of the SkyLAB 752 instrument in the U.S.
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Met key project guidelines of the Joint Product Development Agreement
(JPDA) with ELITech, advancing several products expected to be
released prior to end of fiscal year
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Conducted advanced clinical studies of Lassa virus products in West
Africa in preparation of product launch spanning Q2 and Q3.
First Quarter Conference Call Details
Corgenix invites all those interested in hearing management’s discussion
of the first quarter results to join a shareholders conference call
today, Tuesday, November 13, 2012, at 4:00 p.m. EST (2:00 p.m. MST).
Interested parties can join the call by dialing (800) 895-0231.
International participants may access the call by dialing +1
785-424-1054. The conference code is “CORGENIX.” A replay will be
available for 30 days following the call by dialing (800) 388-5895 for
U.S. participants and +1 402-220-1110 for international participants.
About Corgenix Medical Corporation
Corgenix is a leader in the development and manufacturing of specialized
diagnostic kits for immunology disorders, vascular diseases and bone and
joint disorders, including the world’s only non-blood-based test for
aspirin effect. Corgenix diagnostic products are commercialized for use
in clinical laboratories throughout the world. The company currently
sells over 50 diagnostic products through a global distribution network
and has significant experience advancing products through the FDA
process. More information is available at www.corgenix.com.
Statements in this press release that are not strictly historical
facts are “forward-looking” statements (identified by the words
“believe”, “estimate”, “project”, “expect” or similar expressions)
within the meaning of the Private Securities Litigation Reform Act of
1995. Such statements, which are inherently uncertain, are based on
management’s current expectations and are subject to various factors,
risks and uncertainties that may cause actual results, outcome of
events, timing and performance to differ materially from those expressed
or implied by such forward-looking statements. Factors that would cause
or contribute to such differences include, but are not limited to,
continued acceptance of the Company’s products and services in the
marketplace, competitive factors, changes in the regulatory environment,
and other risks detailed in the Company’s periodic reports filed with
the Securities and Exchange Commission, and in the Company’s subsequent
filings with the Securities and Exchange Commission. The statements in
this press release are made as of today, based upon information
currently known to management, and the Company does not undertake any
obligation or intend to publicly update or revise any forward-looking
statements.
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UNAUDITED SUMMARY BALANCE SHEET DATA (in thousands)
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September 30, 2012
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June 30, 2012
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Cash
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$
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1,197
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$
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1,249
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Working capital
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3,994
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3,645
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Total assets
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6,735
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6,263
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Long-term debt
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440
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472
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Total stockholders’ equity
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4,982
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4,626
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