MISSISSAUGA, ON, May 12 /PRNewswire-FirstCall/ -- DRAXIS Health Inc. (TSX: DAX) reported first quarter operating results that reached new highs for quarterly revenues, product sales and operating income for the three months ended March 31, 2005. All amounts are expressed in U.S. dollars.
Highlights
- Revenues were $22.8 million in the first-quarter, up 62% from
$14.1 million in 2004; driven by record quarterly product sales of
$20.5 million, which were 68% ahead of sales in the first-quarter
2004.
- Net income for the first-quarter 2005 was $3.3 million, up 137% from
$1.4 million in the same quarter the prior year.
- Basic and diluted EPS was 8 cents for the first-quarter 2005; double
the 4 cents per share in the first three months of 2004.
- Operating income for the first quarter 2005 was $4.5 million, up
204% from the $1.5 million in the first-quarter 2004.
- Net cash flows from operating activities increased to $1.6 million
for the first-quarter 2005, compared to a small net cash outflow for
the same period in 2004.
"The first three months of 2005 have seen us achieve the best quarterly operating performance since we acquired our two core operating businesses in 1997 and 1998," said Dr. Martin Barkin, President and CEO of DRAXIS. "The success of our business strategy continues to evolve: operating income is three times what it was a year ago, our operating margins continue to improve, and we are consistently generating positive operating cash flows quarter over quarter. Of our two operations, contract manufacturing continues to take the lead, growing 90% over last year's first-quarter and posting an operating margin of 19.4% as a result of our continuing focus in the specialized production of sterile products. Radiopharmaceutical product sales in first-quarter 2005 were 9% ahead of first-quarter 2004, but this was lower than we anticipated. We have made some significant organizational changes in this division, placing it under new leadership by recently appointing Jean-Pierre Robert as President of DRAXIMAGE."
In the first-quarter 2005 revenues included $0.9 million of contingent milestones earned in respect of product rights sold as part of the 2003 divestiture of the company's Canadian prescription pharmaceutical sales and marketing business. Basic EPS excluding this payment would be 7 cents per share for the first-quarter 2005.
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FINANCIAL HIGHLIGHTS
(in thousands of U.S. dollars except share related data and
in accordance with U.S. GAAP)
Q1, 2005 Q1, 2004
(unaudited) (unaudited)
REVENUES
Product sales $20,506 $12,209
Royalty and licensing 2,339 1,927
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$22,845 $14,136
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Research and development expense $567 $461
Product Gross Margin $7,446 $4,238
Product Gross Margin % 36.3% 34.7%
Operating income $4,540 $1,451
Operating Margin % 19.9% 10.3%
Cash and cash equivalents $7,342 $10,539
Total debt $0 $10,156
Cash flows from (used in) operating
activities $1,606 ($30)
Cash flows used in investing activities (941) (645)
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$665 ($675)
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Net income (loss)
from continuing operations $3,295 $1,388
from discontinued operations - (9)
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$3,295 $1,379
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Basic income per share
from continuing operations $0.080 $0.040
from discontinued operations - -
-------------------------------------------------------------------------
$0.080 $0.040
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Segment Highlights from Management's Discussion and Analysis
Contract Manufacturing
- Product sales revenues of $15.9 million in the first-quarter 2005
represented an increase of $7.5 million, or 90%, over first-quarter
2004 product sales of $8.4 million; the increase was due largely to
increased demand for production of Hectorol(R) Injection for Bone Care
International, Inc. and products under the GlaxoSmithKline contract.
- Product gross margin for the first three months of 2005 was 29.0%
compared to 21.2 % for the same quarter in 2004, the increase being
driven principally by volume growth of higher margin sterile products.
- Operating income was $3.1 million for the first-quarter 2005 compared
to $0.5 million for the first three months of 2004 as a result of both
volume growth, which was made possible by increasing capacity through
additional production labour, and improved capacity utilization that
has directly resulted in better margins through substantially improved
absorption of overhead costs.
- During the quarter the division finalized the studies and analysis
required to support the final validation of the recently installed
second lyophilizer unit and commenced commercial production of
freeze-dried sterile products at the beginning of the second-quarter
2005.
Radiopharmaceuticals
- Product sales for first-quarter 2005 were $4.7 million, a 9.3%
increase over the $4.3 million for first-quarter 2004; primarily as a
result of additional sales of radioiodine products, particularly in
the United States.
- Product gross margin for the first three months of 2005 increased
slightly to 59.1%, compared to 58.5% for the first-quarter 2004,
reflecting the positive impact of sodium iodide sales in both years.
- On April 26, 2005, Mr. Jean-Pierre Robert was appointed the new
President of DRAXIMAGE, the radiopharmaceuticals business, reporting
to the Chief Executive Officer effective May 9, 2005. Mr. Robert has
prior healthcare industry experience, particularly in the
radiopharmaceutical sector, having served as Vice President and
General Manager of Tyco Healthcare (Canada) following its acquisition
of Mallinckrodt (Canada), where he held the same position.
- Dr. Richard Flanagan will assume the position of Scientific Advisor to
the CEO where he will continue to give the Company the benefits of his
in-depth scientific knowledge and experience in radiopharmaceuticals
and molecular imaging.
- During the quarter the division received the first European regulatory
approval for a diagnostic imaging kit product, MAA, which represents a
significant milestone in the strategy of introducing products into
European markets.
- Subsequent to the end of the quarter, DRAXIS provided an update on the
key aspects of the product development program for FIBRIMAGE(R),
including the status of the Canadian Phase III clinical trial, the
findings of two recently completed marketing studies by DRAXIS and the
status of the clinical trial that is planned for the U.S.
Interim Financial Report
This release includes by reference the first-quarter interim financial report incorporating the full Management's Discussion & Analysis (MD&A) as well as financial statements prepared in accordance with U.S. GAAP. The interim report, including the MD&A and financial statements, has been filed with applicable Canadian and U.S. securities regulatory authorities, is accessible on the Company's website at http://www.draxis.com/ in the Investor Relations section under Financial Reports, through the SEDAR and EDGAR databases and is available upon request by contacting DRAXIS Investor Relations at 1-877-441-1984.
Conference Call
DRAXIS has scheduled a conference call to discuss first-quarter 2005 financial results at 10 a.m. (ET) on May 12, 2005. This call can be accessed by dialing 1 (800) 565-5442 (Access Code 1420492) and will also be webcast live with access through the Company's website at http://www.draxis.com/. The conference call will also be available in archived format on the website for 30 days following the conference call.
About DRAXIS Health Inc.
DRAXIS Health (http://www.draxis.com/) is a specialty pharmaceutical company providing products in three categories. Sterile products include liquid and freeze-dried (lyophilized) injectables plus sterile ointments and creams. Non-sterile products are produced as solid oral and semi-solid dosage forms. Radiopharmaceuticals are used for both therapeutic and diagnostic molecular imaging applications.
Pharmaceutical contract manufacturing services are provided through the DRAXIS Pharma division and radiopharmaceuticals are developed, produced, and sold through the DRAXIMAGE division. DRAXIS Health employs over 500 staff in its Montreal facility.
This news release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements are not guarantees of future performance. By their nature, forward-looking statements involve numerous assumptions, known and unknown risks, uncertainties and other factors that may cause the actual results or performance of the Company to be materially different from such statements or from any future results or performance implied thereby. Factors which could cause the Company's results or performance to differ from current expectations include, but are not limited to: the achievement of desired clinical trial results related to the Company's pipeline products; timely regulatory approval of the Company's products; the ability to comply with regulatory requirements applicable to the manufacture and marketing of the Company's products; the Company's ability to obtain and enforce effective patents; the non-infringement of third party patents or proprietary rights by the Company and its products; factors beyond our control which could cause interruptions in our operations; reimbursement policies related to health care; the establishment and maintenance of strategic collaborative and commercial relationships; the Company's dependence on a small number of key customers; the disclosure of confidential information by our collaborators, employees or consultants; the preservation of healthy working relationships with the Company's union and employees; the Company's ability to grow the business; the fluctuation of our financial results and exchange and interest rate fluctuations; the adaptation to changing technologies; the loss of key personnel; the avoidance of product liability claims; the loss incurred if the current lawsuit against us succeeds; the volatility of the price of our common shares; and market acceptance of the Company's products. For additional information with respect to certain of these and other factors, reference should be made to the Company's most recent Form 20-F filed with the United States Securities and Exchange Commission (available on EDGAR at http://www.sec.gov/) and with Canadian securities regulators (available on SEDAR at http://www.sedar.com/). Unless otherwise required by applicable securities laws, the Company disclaims any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.
Financial Tables Attached
DRAXIS HEALTH INC.
Consolidated Statements of Operations
In Accordance with U.S. GAAP
-------------------------------------------------------------------------
(in thousands of U.S. dollars except share related data)
(unaudited)
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
REVENUES
Product sales $ 20,506 $ 12,209
Royalty and licensing 2,339 1,927
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22,845 14,136
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EXPENSES
Cost of goods sold, excluding depreciation
and amortization 13,060 7,971
Selling, general and administration 3,640 3,292
Research and development 567 420
Depreciation and amortization 1,038 961
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18,305 12,644
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Operating income 4,540 1,492
Financing expense, net (42) (125)
Other income - 96
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Income before undernoted 4,498 1,463
Income taxes (1,203) (71)
Minority interest - (4)
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Income from continuing operations 3,295 1,388
Loss from discontinued operations,
net of taxes (Note 2) - (9)
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Net income $ 3,295 $ 1,379
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Basic income (loss) per share
-----------------------------
from continuing operations $ 0.08 $ 0.04
from discontinued operations - -
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$ 0.08 $ 0.04
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Diluted income (loss) per share
-------------------------------
from continuing operations $ 0.08 $ 0.04
from discontinued operations - -
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$ 0.08 $ 0.04
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Weighted-average number of shares
outstanding
- basic 41,142,854 37,537,205
- diluted 42,150,678 38,778,477
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See the accompanying notes to the Consolidated Financial Statements.
These interim financial statements should be read in conjunction with the
annual Consolidated Financial Statements.
DRAXIS HEALTH INC.
Consolidated Balance Sheets
In Accordance with U.S. GAAP
-------------------------------------------------------------------------
(in thousands of U.S. dollars except share related data)
(unaudited)
March 31, December 31,
2005 2004
-------------- -------------
ASSETS (audited)
Current assets
Cash and cash equivalents $ 7,342 $ 5,926
Restricted cash 428 428
Accounts receivable 14,348 13,724
Inventories 9,102 10,158
Prepaid expenses 936 830
Deferred income taxes, net 4,121 4,121
-------------------------------------------------------------------------
Total current assets 36,277 35,187
Property, plant and equipment, net 43,615 43,857
Goodwill, net 707 728
Intangible assets, net 587 737
Other assets 612 604
Deferred income taxes, net 6,643 7,672
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Total assets $ 88,441 $ 88,785
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LIABILITIES
Current liabilities
Accounts payable and accrued liabilities $ 7,110 $ 10,436
Current portion of deferred revenues 3,705 3,676
Customer deposits 608 628
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Total current liabilities 11,423 14,740
Deferred revenues 3,301 4,125
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Total liabilities $ 14,724 $ 18,865
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Minority interest (Note 3) - -
SHAREHOLDERS' EQUITY
Common stock, without par value of
unlimited shares authorized $ 76,598 $ 75,840
Additional paid-in capital 15,546 15,546
Warrants (Note 4(c)) 916 916
Deficit (24,270) (27,565)
Accumulated other comprehensive income 4,927 5,183
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Total shareholders' equity 73,717 69,920
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Total liabilities and shareholders' equity $ 88,441 $ 88,785
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See the accompanying notes to the Consolidated Financial Statements.
These interim financial statements should be read in conjunction with the
annual Consolidated Financial Statements.
DRAXIS HEALTH INC.
Consolidated Statements of Changes in Equity and Comprehensive
Income (Loss)
In Accordance with U.S. GAAP
-------------------------------------------------------------------------
(in thousands of U.S. dollars except share related data)
(unaudited)
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
Common Stock (Number of Shares)
Balance, beginning of period 41,015,326 37,297,817
Exercise of options 289,062 402,532
Exercise of employee participation shares - 54,896
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Balance, end of period 41,304,388 37,755,245
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Common Stock
Balance, beginning of period $ 75,840 $ 61,175
Exercise of options 758 1,173
Exercise of employee participation shares - 204
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Balance, end of period $ 76,598 $ 62,552
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Additional Paid In Capital
Balance, beginning of period $ 15,546 $ 15,667
Stock compensation - (121)
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Balance, end of period $ 15,546 $ 15,546
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Warrants
Balance, beginning of period $ 916 $ -
-------------------------------------------------------------------------
Balance, end of period $ 916 $ -
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Employee Participation Shares
Balance, beginning of period $ - $ 86
Exercise of employee participation shares - (86)
-------------------------------------------------------------------------
Balance, end of period $ - $ -
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Employee Participation Shares-Loans Receivable
Balance, beginning of period $ - $ (86)
Exercise of employee participation shares - 86
-------------------------------------------------------------------------
Balance, end of period $ - $ -
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Deficit
Balance, beginning of period $ (27,565) $ (35,481)
Net income 3,295 1,379
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Balance, end of period $ (24,270) $ (34,102)
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Accumulated Other Comprehensive Income (Loss)
Balance, beginning of period $ 5,183 $ 286
Other comprehensive loss (256) (594)
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Balance, end of period 4,927 (308)
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Total shareholders' equity $ 73,717 $ 43,688
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Comprehensive Income
Foreign currency translation adjustments $ (256) $ (594)
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Other comprehensive loss (256) (594)
Net income 3,295 1,379
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Total comprehensive income $ 3,039 $ 785
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See the accompanying notes to the Consolidated Financial Statements.
These interim financial statements should be read in conjunction with the
annual Consolidated Financial Statements.
DRAXIS HEALTH INC.
Consolidated Statements of Cash Flows
In Accordance with U.S. GAAP
-------------------------------------------------------------------------
(in thousands of U.S. dollars)
(unaudited)
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
CASH FLOWS FROM (USED IN) OPERATING
ACTIVITIES
Net income from continuing operations $ 3,295 $ 1,388
Adjustments to reconcile net income from
continuing operations to net cash
from (used in) operating activities
Amortization of deferred revenues (1,050) (1,318)
Depreciation and other amortization 1,038 961
Stock compensation - 83
Deferred income taxes 987 (32)
Minority interest - 4
Other 261 315
Changes in operating assets and liabilities
Accounts receivable (630) (654)
Inventories 1,003 (1,128)
Income taxes (37) 118
Prepaid expenses (206) (190)
Accounts payable and accrued liabilities (3,309) 325
Current portion of deferred revenues 254 98
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Net cash from (used in) operating activities
of continuing operations 1,606 (30)
-------------------------------------------------------------------------
CASH FLOWS FROM (USED IN) INVESTING
ACTIVITIES
Expenditures for property, plant and
equipment (794) (591)
Increase in intangible assets (147) (150)
Proceeds from disposition of product right - 96
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Net cash from (used in) investing activities of
continuing operations (941) (645)
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CASH FLOWS FROM (USED IN) FINANCING ACTIVITIES
Repayment of long-term debt - (241)
(Decrease) increase from customer
deposits, net (17) 16
Exercise of options 758 1,173
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Net cash from (used in) financing activities
of continuing operations 741 948
-------------------------------------------------------------------------
Effect of foreign exchange rate changes
on cash and cash equivalents 10 (284)
-------------------------------------------------------------------------
Net cash from (used in) continuing
operations 1,416 (11)
Net cash used in discontinued operations - (13)
-------------------------------------------------------------------------
Net increase (decrease) in cash and
cash equivalents 1,416 (24)
Cash and cash equivalents, beginning of
period 5,926 10,563
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Cash and cash equivalents, end of period $ 7,342 $ 10,539
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Additional Information
Interest paid $ - $ 71
Income taxes paid $ 228 $ 154
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See the accompanying notes to the Consolidated Financial Statements.
These interim financial statements should be read in conjunction with the
annual Consolidated Financial Statements
DRAXIS HEALTH INC.
Notes to the Consolidated Financial Statements
In Accordance with U.S. GAAP
-------------------------------------------------------------------------
(in thousands of U.S. dollars except share related data)
(unaudited)
1. Significant Accounting Policies
These consolidated financial statements have been prepared in
accordance with U.S. generally accepted accounting principles
("GAAP").
The functional currency of the Company is the Canadian dollar however
its reporting currency is the U.S. dollar. For the current and prior
periods, the financial statements of the Company's operations whose
reporting currency is other than the U.S. dollar are translated from
such reporting currency to U.S. dollars using the current rate
method. Under the current rate method, assets and liabilities are
translated at the exchange rates in effect at the balance sheet date.
Revenues and expenses, including gains and losses on foreign exchange
transactions, are translated at average rates for the period. The
resulting unrealized translation gains and losses on the Company's
net investment in these operations, including long-term intercompany
advances, are accumulated in a separate component of shareholders'
equity, described in the consolidated balance sheets as accumulated
other comprehensive income.
The disclosures contained in these unaudited interim consolidated
financial statements do not include all requirements of GAAP for
annual financial statements. The unaudited interim consolidated
financial statements should be read in conjunction with the audited
consolidated financial statements for the year ended
December 31, 2004.
The unaudited interim consolidated financial statements are based
upon accounting principles consistent with those used and described
in the audited consolidated financial statements for the year ended
December 31, 2004, other than as noted herein.
The unaudited interim consolidated financial statements reflect all
adjustments, consisting only of normal recurring adjustments, which
are, in the opinion of management, necessary to present fairly the
financial position of the Company as at March 31, 2005 and the
results of operations and cash flows for the three month periods
ended March 31, 2005 and 2004.
2. Discontinued Operations
In 2001, the Company adopted a formal plan to dispose of its Canadian
sales and marketing division ("DRAXIS Pharmaceutica").
Pursuant to APB No. 30, "Reporting the Results of Operations -
Reporting the Effects of Disposal of a Segment of a Business, and
Extraordinary, Unusual and Infrequently Occurring Events and
Transactions," the results of operations of DRAXIS Pharmaceutica have
been reported as discontinued operations and the consolidated
financial statements and notes thereto for the year ended
December 31, 2001 and all subsequent periods presented have been
reclassified.
On March 31, 2003, the Company amended its License, Distribution and
Supply Agreement with Elan Corporation, plc ("Elan") to return the
Canadian rights to several of Elan's neurology products in exchange
for a cash payment of $6,500, resulting in an after tax gain of
$4,286 on this transaction.
On July 22, 2003, the Company completed the divestiture of DRAXIS
Pharmaceutica with the sale to Shire BioChem Inc. ("Shire"), of
substantially all remaining products of the division. The Company
received $9,600 in cash from Shire and could receive up to $2,900 in
market driven milestones over the next several years. The Company
realized an after tax gain of $4,054, net of transaction and related
charges. In addition, the Company will receive royalty payments based
on the continuing Canadian sales of the products. The Company also
received the value of acquired inventories and Shire is now
responsible for all financial provisions of the license agreement
related to Permax(R).
Commencing in the second quarter of 2002, the Company resolved to
retain ownership of the Canadian rights to Alertec(R) and continue to
market and sell Alertec(R) in Canada itself. Accordingly,
discontinued operations did not include revenues and expenses
directly attributable to Alertec(R) up until such time that third
party approval was obtained. As a result of the ability to obtain
third party approval upon closing with Shire, management decided to
dispose of Alertec(R) through the sale of the Canadian rights to
Shire and at that time included Alertec(R) as part of discontinued
operations on a prospective basis.
Interest expense directly attributable to license obligations
included in the transaction has been allocated to the discontinued
operations.
The results of discontinued operations, presented in the accompanying
Consolidated Statements of Operations, were as follows:
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
Revenues $ - $ 73
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Operating loss from discontinued
operations - (13)
Income tax recovery - 4
---------------------------------------------------------------------
Net loss from discontinued operations
- net of tax $ - $ (9)
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3. Acquisition of Minority Interest
On April 22, 2004, the Company completed the acquisition of the 32.7%
interest in the Company's manufacturing subsidiary, DRAXIS Pharma
Inc. ("DPI"), that was previously owned by SGF Sante Inc. ("SGF").
The $9.6 million (CDN$13.0 million) cash acquisition has been
accounted for by the purchase method of accounting and allocated to
identifiable assets and liabilities based on their estimated fair
values as follows:
Minority interest $3,992
Property, plant and equipment 6,785
Deferred income tax liability (1,220)
----------------------------------------
Total purchase price $9,557
----------------------------------------
----------------------------------------
The estimates of fair value were determined by the Company's
management based on an independent valuation of Property, plant and
equipment.
The purchase price paid to SGF is subject to adjustment in limited
circumstances involving a change of control of the Company or DPI or
a sale of substantially all of the assets of DPI prior to
April 22, 2005.
4. Shareholders' Equity
(a) Stock Option Plan
The following is a summary of common shares issuable pursuant to
outstanding stock options:
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
Balance, beginning of period 2,753,232 3,097,942
Increase (decrease) resulting from:
Granted 325,000 125,000
Exercised (289,062) (400,032)
Cancelled - (68,333)
Expired - (1,700)
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Balance, end of period 2,789,170 2,752,877
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(b) Stock-based Compensation Costs
The following outlines the impact and assumptions used if the
compensation cost for the Company's stock options was determined
under the fair value based method of accounting.
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
Net income, as reported $ 3,295 $ 1,379
Pro forma impact (201) (167)
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Pro forma net income $ 3,094 $ 1,212
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Basic net income per share, as reported $ 0.08 $ 0.04
Pro forma impact per share - (0.01)
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Pro forma net income per share (Basic) $ 0.08 $ 0.03
Pro forma net income per share (Diluted) $ 0.07 $ 0.03
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Dividend yield 0.0% 0.0%
Expected volatility 59-60% 60%-62%
Risk-free interest rate 4.0% 4.0%
Expected option life 5 yrs 5yrs
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(c) Common Share Offering
On April 22, 2004, the Company closed its offering of 3,053,436 units
at a price of $4.82 (CDN$6.55) per unit for proceeds net of related
expenses of $13,385 (CDN$18,213). Each unit consists of one common
share of the Company and one-half of one share purchase warrant. Each
whole warrant will entitle the holder to acquire one common share of
the Company at a price of CDN$8.50 at any time prior to two years
from April 22, 2004. Included as a component of shareholders' equity
is $916, which represents the fair value of the warrants issued. The
fair value of the warrant was determined based on the price of the
offering.
The underwriters had an over-allotment option to purchase up to an
additional 458,016 units, exercisable at the issue price any time up
to 30 days following closing of the offering, representing additional
gross proceeds of up to $2,206 (CDN$3,000) to the Company. The
over-allotment option expired unexercised.
5. Segmented Information
Industry Segmentation
For purposes of decision-making and assessing performance, management
considers that it operates in three segments: Radiopharmaceuticals,
Manufacturing, and Corporate and Other. Executive management assesses
the performance of each segment based on segment income before
financing expense, income taxes and minority interest. The
accounting policies used to determine segmented results and measure
segmented assets are the same as those described in the summary of
significant accounting policies
For the Three Month Periods
Ended March 31,
----------------------------
2005 2004
-------------- -------------
PRODUCT SALES REVENUES
Radiopharmaceuticals $ 4,734 $ 4,332
Manufacturing 15,851 8,363
Corporate and Other (79) (486)
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$ 20,506 $ 12,209
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ROYALTY AND LICENSING REVENUES
Radiopharmaceuticals $ - $ -
Manufacturing - -
Corporate and Other 2,339 1,927
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$ 2,339 $ 1,927
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TOTAL REVENUES
Radiopharmaceuticals $ 4,734 $ 4,332
Manufacturing 15,851 8,363
Corporate and Other 2,260 1,441
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$ 22,845 $ 14,136
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PRODUCT GROSS MARGIN
Radiopharmaceuticals $ 2,797 $ 2,534
Manufacturing 4,600 1,773
Corporate and Other 49 (69)
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$ 7,446 $ 4,238
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SELLING, GENERAL AND ADMINISTRATION
EXPENSE
Radiopharmaceuticals $ 1,136 $ 839
Manufacturing 849 846
Corporate and Other 1,655 1,607
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$ 3,640 $ 3,292
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RESEARCH AND DEVELOPMENT EXPENSE
Radiopharmaceuticals $ 567 $ 420
Manufacturing - -
Corporate and Other - -
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$ 567 $ 420
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DEPRECIATION AND AMORTIZATION
Radiopharmaceuticals $ 245 $ 227
Manufacturing 681 466
Corporate and Other 112 268
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$ 1,038 $ 961
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OPERATING INCOME (LOSS)
Radiopharmaceuticals $ 849 $ 1,048
Manufacturing 3,070 461
Corporate and Other 621 (17)
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$ 4,540 $ 1,492
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IDENTIFIABLE ASSETS March 31, December 31,
2005 2004
-------------- -------------
(audited)
Radiopharmaceuticals $ 11,963 $ 12,354
Manufacturing 49,098 50,103
Corporate and Other 27,380 26,328
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$ 88,441 $ 88,785
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Geographic Segmentation
For the Three Month Periods
Ended March 31,
----------------------------
REVENUES(1) 2005 2004
-------------- -------------
Canada $ 11,354 $ 6,586
United States 11,367 7,440
Other 124 110
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$ 22,845 $ 14,136
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March 31, December 31,
LONG-LIVED ASSETS(2) 2005 2004
-------------- -------------
(audited)
Canada $ 44,909 $ 45,322
United States - -
---------------------------------------------------------------------
$ 44,909 $ 45,322
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(1) Revenues are attributable to countries based upon the location
of the customer.
(2) Represents property, plant and equipment, goodwill and intangible
assets that are identified with each geographic region.
For the Three Month Periods
Ended March 31,
----------------------------
EXPENDITURES FOR PROPERTY, PLANT
AND EQUIPMENT 2005 2004
-------------- -------------
Radiopharmaceuticals $ 44 $ 209
Manufacturing 739 371
Corporate and Other 11 11
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$ 794 $ 591
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For the Three Month Periods
Ended March 31,
----------------------------
PRODUCT SALES REVENUES BY MAJOR
PRODUCT GROUPS 2005 2004
-------------- -------------
Radiopharmaceuticals $ 4,734 $ 4,332
Manufacturing - Sterile 11,337 5,717
Manufacturing - Non Sterile 4,514 2,646
Corporate and Other 166 1
Intercompany eliminations (245) (487)
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$ 20,506 $ 12,209
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6. Reconciliation of Results Reported in Accordance with U.S. GAAP to
Canadian GAAP
The major differences between U.S. and Canadian GAAP which affect net
income are summarized in the following table with an explanation of
the adjustments.
For the Three Month Periods
Ended March 31,
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2005 2004
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Net income as reported under U.S. GAAP $3,295 $1,379
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Continuing operations
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Intangible assets - Radiopharmaceuticals
segment, net of tax (i) 54 (84)
Intangible assets - Corporate and Other
segment, net of tax (i) (518) (518)
Stock-based compensation (ii) (201) (140)
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(665) (742)
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Net income under Canadian GAAP $2,630 $637
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Basic income (loss) per share
Canadian GAAP $0.06 $0.02
U.S. GAAP $0.08 $0.04
Diluted income (loss) per share
Canadian GAAP $0.06 $0.02
U.S. GAAP $0.08 $0.04
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(i) Intangible Assets - Continuing Operations
Amortization expense associated with continuing operations
under U.S. GAAP differs from Canadian GAAP due to the
differential treatment of the excess of the purchase cost over
the fair value of the assets acquired in conjunction with the
1996 acquisition of Deprenyl Animal Health, Inc., which was
treated as acquired research and development, and the portion
of the 1997 acquisition cost of the Company's
radiopharmaceutical business assigned to acquired research and
development.
(ii) Stock-Based Compensation
Under Canadian GAAP, the Company, in the first quarter of 2004,
adopted retroactively with restatement of 2002 and 2003
results, the application of the fair value based method for
measuring the compensation cost of employee stock options
granted in 2002 and beyond. Under U.S. GAAP, the Company has
elected to adopt the optional recognition provision for its
stock options plans and hence the cost of employee stock
options is disclosed in the note to the financial statements as
pro forma earnings and per share information. The difference
between U.S. and Canadian GAAP applicable to stock-based
compensation applies only to the Corporate and Other segment.
(iii) Research and Development
Under Canadian GAAP, investment tax credits on research and
development are deducted from research and development expense.
Under U.S. GAAP, investment tax credits are recorded as a
reduction of the income tax expense. As a result, there is no
impact in the reconciliation of net income or shareholders'
equity from U.S. to Canadian GAAP.
7. Comparative Information
The Company has reclassified certain prior period's information to
conform with the current presentation format.
DRAXIS Health Inc.