













Paladin Reports First Quarter 2012 Results Achieves Record Revenues
Published in Health and Fitness on Thursday, May 3rd 2012 at 4:19 GMT by Market Wire

May 03, 2012 07:00 ET
Paladin Reports First Quarter 2012 Results Achieves Record Revenues
MONTREAL, CANADA--(Marketwire - May 3, 2012) - Paladin Labs Inc. (TSX:PLB), a leading specialty pharmaceutical company, today reported its financial results for the quarter ended March 31, 2012.
2012 First Quarter Highlights
Financial
- Revenues reached a record $38.6 million, an increase of 21% over the same period last year
- Net income was $11.3 million, an increase of 40% over the same period last year
- EBITDA1 was $18.0 million, an increase of 4% over the same period last year
Product Development
- Filed a new drug submission (NDS) that has been accepted for review by Health Canada for Silenor® (doxepin) for the treatment and symptomatic relief of insomnia
- Received regulatory approval from Health Canada for Oralair™, a sublingual grass pollen immunotherapy tablet for the treatment of the symptoms of moderate to severe seasonal grass pollen allergic rhinitis with or without conjunctivitis
Corporate Development
- Entered into a strategic partnership whereby the Company will accelerate the buy-out of Pharmaplan (Pty) Limited ("Pharmaplan") and merge the Pharmaplan business with the pharma division of Litha Healthcare Group Limited (JSE:LHG) ("Litha")
"The first quarter of 2012 was marked by important business development and regulatory activities. We are pleased that our partnership agreement with Litha remains on track to close in early July and, on closing, will further expand Paladin's geographic footprint and our international growth prospects. We expect the transaction will be immediately accretive and result in a step change in Paladin's financial profile. During the quarter, we received regulatory approval for Oralair™, a novel sublingual grass pollen immunotherapy tablet. We also submitted our insomnia treatment, Silenor®, for regulatory approval. With our robust product pipeline and strong balance sheet we are confident in our ability to continue to execute our growth strategy" said Mark Beaudet, interim President and CEO of Paladin Labs.
Financial Results
Revenues increased $6.8 million or 21% to $38.6 million for the first quarter of 2012 from $31.8 million for the same period in 2011. The increase in revenues for the first quarter is primarily due to incremental revenues from products acquired and/or launched after the comparative quarter, March 31, 2011, which contributed $3.4 million to the quarter ended March 31, 2012. The increase in revenues is also attributable to the sales growth of certain significant promoted products, including Tridural®, Trelstar®, Testim®, Metadol®, Plan B® and Abstral®, which combined increased by 9% compared to 2011.
First quarter 2012, EBITDA1 increased 4% to $18.0 million, compared to EBITDA1 of $17.3 million in the first quarter of 2011.
Net income for the quarter was $11.3 million or $0.54 per fully diluted share, compared to net income of $8.1 million or $0.40 per fully diluted share in the first quarter a year ago.
As at March 31 2012, Paladin's cash, cash equivalents and investments in marketable securities totaled a record $252.7 million. From this strong cash position, Paladin continues to pursue acquisition opportunities.
Product Developments
During the quarter Paladin filed a NDS with Health Canada for Silenor® and received regulatory approval from Health Canada for Oralair™.
In February 2012, Paladin announced that it filed a NDS for Silenor® with Health Canada and that Health Canada had accepted the submission for review. Silenor® is a low-dose oral tablet formulation of doxepin indicated for the treatment and symptomatic relief of insomnia. If approved, Silenor® is expected to be the first and only non-controlled prescription sleep medication in Canada indicated for the treatment and symptomatic relief of insomnia characterized by difficulty in falling asleep, frequent nocturnal awakening and/or early morning awakenings.
In March 2012, Paladin received regulatory approval for Oralair™. Oralair™ is a sublingual grass pollen immunotherapy tablet for the treatment of the symptoms of moderate to severe seasonal grass pollen allergic rhinitis with or without conjunctivitis. Paladin anticipates launching Oralair™ in time for the 2013 allergy season and is confident that, when launched, Oralair™ will provide Canadian allergy sufferers with a safe, effective and convenient alternative for the treatment of seasonal grass allergies.
Corporate Developments
In February, 2012, Paladin entered into a strategic partnership whereby it will accelerate the buy-out of the remaining 55.01% of Pharmaplan and merge the Pharmaplan business with the pharma division of Litha (the "Combined Transactions"). Under the terms of the Combined Transactions, Paladin will acquire the 55.01% of Pharmaplan which it does not currently own. Litha will then acquire 100% of the share capital of Pharmaplan from Paladin in exchange for cash and the issuance of 169,090,909 shares in Litha at ZAR2.75 per share. Paladin has also agreed to acquire an additional 72,989,078 shares of Litha from the Blackstar Group at ZAR2.75 per share. Paladin will deploy an anticipated $48 million in cash and issue 88,948 shares at $44.97 per share to complete the Combined Transactions. As a result Paladin will own approximately 45% of Litha, making it Litha's single largest shareholder upon closing. The Combined Transactions are subject to certain regulatory approvals including South African competition review and approval by shareholders of Litha and is expected to close on July 2, 2012.
Had the Combined Transactions taken place on January 1, 2011, Paladin would have recorded $255 million of consolidated revenue and $96 million of consolidated EBITDA, an increase of $113 million and $28 million, respectively, over its reported revenue of $141.5 million and EBITDA of $67.6 million for the year ended December 31, 2011. These amounts do not give effect to the interest in Litha not owned by Paladin.
During 2011, Paladin received regulatory approval from the Toronto Stock Exchange to carry out a normal course issuer bid and to date has purchased 75,420 shares under this normal course issuer bid.
Jonathan Goodman Update
On August 18, 2011, the Company announced that its President and CEO, Mr. Jonathan Ross Goodman, was involved in an accident and was hospitalized with serious injuries. As Mr. Goodman was unable to perform his duties as President and CEO, the Board of Directors of Paladin asked Mr. Mark Beaudet, Co-Founder, Director and Vice President Marketing and Sales of Paladin, to assume such duties on an interim basis. Mr. Goodman continues his recovery and rehabilitation program. As a result, Mr. Goodman will remain absent from the Company for an indeterminate period of time. The Company will provide further updates on Mr. Goodman's condition only when a change in circumstance warrants same.
(1) EBITDA - Non-IFRS Financial Measures
The term EBITDA (earnings before interest, taxes, depreciation and amortization) does not have any standardized meaning under International Financial Reporting Standards ("IFRS") and therefore may not be comparable to similar measures presented by other companies. The Company defines EBITDA as earnings before interest expense, other expense (income), taxes, amortization, foreign exchange gains (losses), share of net income in an associate and unusual items; such as write-downs and gains (losses) on intellectual property and investments. EBITDA is calculated and presented consistently from period to period and agrees, on a consolidated basis, with the amount disclosed as "Earnings before under-noted items" on the consolidated statements of income. The Company believes EBITDA to be an important measurement that allows it to assess the operating performance of its ongoing business on a consistent basis without the impact of amortization expenses. The Company excludes amortization expenses because their level depends substantially on non-operating factors such as the historical cost of intangible assets. The Company's method for calculating EBITDA may differ from that used by other issuers and, accordingly, this measure may not be comparable to EBITDA used by other issuers.
Conference Call Notice
Paladin will host a conference call to discuss its first quarter results today at 10:00 a.m. EST. The dial-in number for the conference call is 1-800-768-2481 or 416-981-9000. The call will be audio-cast live and archived for 30 days at [ www.paladinlabs.com ].
About Paladin Labs Inc.
Paladin Labs Inc., headquartered in Montreal, Canada, is a specialty pharmaceutical company focused on acquiring or in-licensing innovative pharmaceutical products for the Canadian and select international markets. With this strategy, a focused Canadian national sales team and proven marketing expertise, Paladin has evolved into one of Canada's leading specialty pharmaceutical companies. For more information, please visit the Company's web site at [ www.paladinlabs.com ].
This press release may contain forward-looking statements and predictions. These forward-looking statements, by their nature, necessarily involve risks and uncertainties that could cause actual results to differ materially from those contemplated by the forward-looking statements. The Company considers the assumptions on which these forward-looking statements are based to be reasonable at the time they were prepared, but cautions that these assumptions regarding the future events, many of which are beyond the control of the Company and its subsidiaries, may ultimately prove to be incorrect. Factors and risks, which could cause actual results to differ materially from current expectations, are discussed in the annual report as well as in the Company's Annual Information Form for the year ended December 31, 2011. The Company disclaims any intention or obligation to update or revise any forward-looking statements whether as a result of new information or future events and except as required by law. For additional information on risks and uncertainties relating to these forward-looking statements, investors should consult the Company's ongoing quarterly filings, annual report and Annual Information Form and other fillings found on SEDAR at [ www.sedar.com ].
INTERIM CONSOLIDATED BALANCE SHEETS |
[In thousands of Canadian dollars] | ||
As at | March 31, 2012 | December 31, 2011 |
ASSETS | ||
Current | ||
Cash and cash equivalents | 89,402 | 72,115 |
Marketable securities | 163,298 | 166,894 |
Trade and other receivables | 24,825 | 20,208 |
Inventories | 13,101 | 13,327 |
Income tax receivable | 1,412 | 718 |
Other current assets | 2,638 | 1,476 |
Total current assets | 294,676 | 274,738 |
Investment in an associate | 21,275 | 20,850 |
Financial assets | 8,905 | 9,311 |
Investment tax credits recoverable | 24,674 | 24,674 |
Deferred income tax assets | 36,297 | 40,613 |
Property, plant and equipment | 152 | 162 |
Pharmaceutical product licenses and rights | 24,662 | 27,565 |
Total assets | 410,641 | 397,913 |
LIABILITIES AND SHAREHOLDERS' EQUITY | ||
Current | ||
Payables, accruals and provisions | 42,350 | 38,849 |
Finance lease liability | 1,008 | 984 |
Deferred revenue | 3,190 | 2,999 |
Income tax payable | 21,542 | 22,205 |
Balances of sale payable | 849 | 1,809 |
Total current liabilities | 68,939 | 66,846 |
Finance lease liability | 5,467 | 5,745 |
Deferred revenue | 1,861 | 2,099 |
Balances of sale payable | 497 | 497 |
Total liabilities | 76,764 | 75,187 |
Shareholders' equity | ||
Share capital | 167,342 | 166,681 |
Other paid-in capital | 5,494 | 5,144 |
Other capital reserves | 19 | 553 |
Retained earnings | 161,022 | 150,348 |
Total shareholders' equity | 333,877 | 322,726 |
Total liabilities and shareholders' equity | 410,641 | 397,913 |
INTERIM CONSOLIDATED INCOME STATEMENTS | ||||
[In thousands of Canadian dollars except for share and per share amounts] | ||||
Three months ended March 31 | ||||
2012 | 2011 | |||
Revenues | 38,557 | 31,752 | ||
Cost of sales | 11,188 | 8,040 | ||
Gross income | 27,369 | 23,712 | ||
Expenses (income) | ||||
Selling, general and administrative | 7,668 | 7,040 | ||
Research and development | 2,548 | 2,071 | ||
Interest income | (893 | ) | (2,669 | ) |
Earnings before under-noted items | 18,046 | 17,270 | ||
Amortization of pharmaceutical product licenses and rights | 2,903 | 5,330 | ||
Other finance expense | 555 | 573 | ||
Other income | (200 | ) | - | |
Foreign exchange gain | (154 | ) | (381 | ) |
Share of net income of an associate | (425 | ) | (201 | ) |
Income before income tax | 15,367 | 11,949 | ||
Provision for income taxes | 4,045 | 3,849 | ||
Net income for the period | 11,322 | 8,100 | ||
Attributable to shareholders | ||||
Basic earnings per share | 0.56 | 0.42 | ||
Diluted earnings per share | 0.54 | 0.40 | ||
Weighted average number of shares outstanding | ||||
Basic | 20,284,749 | 19,290,851 | ||
Diluted | 20,919,714 | 20,042,756 | ||
INTERIM CONSOLIDATED STATEMENTS OF CASH FLOWS | |||||
[In thousands of Canadian dollars] | Three months ended March 31 | ||||
2012 | 2011 | ||||
Operating activities | |||||
Net income for the year | 11,322 | 8,100 | |||
Adjustments reconciling net income to operating cash flows | |||||
Amortization of pharmaceutical product licenses and rights | 2,903 | 5,330 | |||
Deferred tax | 4,373 | 2,280 | |||
Share-based compensation expense | 581 | 423 | |||
Other finance expense | 555 | 573 | |||
Unrealized foreign exchange loss (gain) | 65 | (470 | ) | ||
Depreciation of property, plant and equipment | 27 | 105 | |||
Share of net income of an associate | (425 | ) | (201 | ) | |
19,401 | 16,140 | ||||
Net change in non-cash balances relating to operations | (4,518 | ) | (1,638 | ) | |
Cash inflow from operating activities | 14,883 | 14,502 | |||
Investing activities | |||||
Disposal and maturities of marketable securities | 39,507 | 2,913 | |||
Purchases of marketable securities | (36,578 | ) | (45,738 | ) | |
Purchase of property, plant and equipment | (16 | ) | (55 | ) | |
Purchase of financial assets | - | (80,338 | ) | ||
Purchase of pharmaceutical product licenses and rights | - | (7,567 | ) | ||
Investment in an associate | - | (2,936 | ) | ||
Repayment of balances of sale payable | - | (250 | ) | ||
Proceeds from disposal of financial assets | - | 3,344 | |||
Dividends from an associate | - | 251 | |||
Net cash inflow (outflow) from investing activities | 2,913 | (130,376 | ) | ||
Financing activities | |||||
Common shares issued for cash, net of issuance costs of $nil [2011: $1,643] | 571 | 39,387 | |||
Repurchase of shares | (819 | ) | - | ||
Repayment of obligation under finance lease | (250 | ) | - | ||
Net cash (outflow) inflow from financing activities | (498 | ) | 39,387 | ||
Foreign exchange loss on cash and cash equivalents | (11 | ) | (167 | ) | |
Increase (decrease) in cash and cash equivalents during the period | 17,287 | (76,654 | ) | ||
Cash and cash equivalents, beginning of the period | 72,115 | 96,295 | |||
Cash and cash equivalents, end of the period | 89,402 | 19,641 | |||
Cash and cash equivalents | 89,402 | 19,641 | |||
Marketable securities | 163,298 | 86,067 | |||
252,700 | 102,708 | ||||