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BioMarin Announces First Quarter 2011 Financial Results Financial Highlights ($ in millions, except per share data, unaudited) Item Q1 2011 Q1 2010 Comparison Total BioMarin Revenue $109.5 28.8% increase...

Key Takeaway: NOVATO, Calif. , April 28, 2011 /PRNewswire/ -- Financial Highlights ($ in millions, except per share data, unaudited) BioMarin Pharmaceutical Inc. (Nasdaq: BMRN ) today announced financial results for the first quarter of 2011. GAAP net loss was $4.4 million ( $0.04 per dilute

Full Press Release Details

NOVATO, Calif. , April 28, 2011 /PRNewswire/ --
Financial Highlights ($ in millions, except per share data, unaudited)
Item Q1 2011 Q1 2010 Comparison
Total BioMarin Revenue $109.5 28.8% increase
Total Net Product Revenue $109.1 29.7% increase
Naglazyme Net Product Revenue $60.6 24.7% increase
Aldurazyme BioMarin Net Product Revenue* $18.7 $14.2
Kuvan Net Product Revenue $26.7 25.9% increase
Firdapse Net Product Revenue $3.1 $0.1
GAAP Net Income (Loss) $(4.4) $1.2
GAAP Net Income (Loss) per share $ (0.04) (basic and diluted) $0.01 (basic and diluted)
Non-GAAP Adjusted EBITDA $17.3 $14.8
Non-GAAP Adjusted EBITDA per share $0.16 (basic), $0.14 (diluted) $0.15 (basic), $0.14 (diluted)
* Net product transfer revenue had a positive $1.8 milli on impact on net Aldurazyme revenue to BioMarin in the first quarter of 2011 and a negative $1.7 million impact on net Aldurazyme revenue to BioMarin in the first quarter of 2010.
BioMarin Pharmaceutical Inc. (Nasdaq: BMRN ) today announced financial results for the first quarter of 2011. GAAP net loss was $4.4 million ( $0.04 per diluted share) for the first quarter of 2011, compared to GAAP net income of $1.2 million ( $0.01 per diluted share) for the first quarter of 2010. Non-GAAP adjusted EBITDA was $17.3 million ( $0.14 per diluted share) for the first quarter of 2011, compared to non-GAAP adjusted EBITDA of $14.8 million ( $0.14 per diluted share) for the first quarter of 2010. Non-GAAP adjusted EBITDA excludes depreciation and amortization, contingent consideration expense, interest income and expense, income taxes, stock compensation expense and material non-recurring items. The reconciliation of the non-GAAP measures to the GAAP net income in the first quarter of 2011 is detailed in the table provided near the end of the press release.
As of March 31, 2011 , BioMarin had cash, cash equivalents and short and long-term investments totaling $394.0 million , as compared to $402.3 million as of December 31, 2010 . Cash and investment balances declined $8.3 million in the first quarter of 2011 due primarily to the timing of cash receipts that were collected in early April. For 2011, the company expects to remain cash flow neutral to slightly positive.
"Our clinical pipeline is advancing with more programs in the clinic than ever in the history of the company," said Jean-Jacques Bienaime , Chief Executive Officer of BioMarin. "We saw a strong quarter from our commercial business, driven in part by the timing of a Naglazyme order from Brazil early in the quarter, along with consistent new patient adds around the world. We remain focused on growing the commercial business and the successful advancement of our pipeline projects."
Net Product Revenue (in millions)
Three Months Ended March 31,
2011 2010 $ Change % Change
Naglazyme (1) $ 60.6 $ 48.6 $ 12.0 24.7%
Kuvan (2) $ 26.7 $ 21.2 $ 5.5 25.9%
Firdapse (3) $ 3.1 $ 0.1 $ 3.0 100%+
(1) Changes in foreign currency rates, net of hedges, had a positive $0.1 million impact on Naglazyme sales in the three months ended March 31, 2011. Naglazyme revenues experience quarterly fluctuations due to the timing of government ordering patterns in certain countries.
(2) The quantity of commercial tablets dispensed to patients in the U.S. increased 21.1 percent in the first quarter of 2011 compared to the first quarter of 2010.
(3) A product for the treatment of Lambert Eaton Myasthenic Syndrome (LEMS) which was launched in the EU in April 2010.
Three Months Ended March 31,
2011 2010 $ Change % Change
Aldurazyme revenue reported by Genzyme (4) $ 42.8 $ 39.9 $ 2.9 7.3%
Royalties due from Genzyme 16.9 15.9 1.0
Incremental (previously recognized) 1.8 (1.7) 3.5
Total Aldurazyme net product revenues (5) $ 18.7 $ 14.2 $ 4.5
(4) Changes in foreign currency rates caused an increase to Aldurazyme sales by Genzyme of $0.4 million in the three months ended March 31, 2011. In the first quarter of 2011, the number of Aldurazyme vials shipped increased 6.4 percent over the first quarter of 2010.
(5) To the extent units shipped to third party customers by Genzyme exceed BioMarin inventory transfers to Genzyme, BioMarin records a decrease in net product revenue from the royalty payable to BioMarin for the amount of previously recognized product transfer revenue. If BioMarin inventory transfers exceed units shipped to third party customers by Genzyme, BioMarin will record incremental net product transfer revenue for the period.
Revenue Guidance ($ in millions)
Item 2011 Guidance Previous 2011 Guidance
Total BioMarin Revenues $422 to $452 $417 to $452
Total Net Product Revenues $416 to $446 $411 to $446
Naglazyme Net Product Revenue $211 to $225 $206 to $225
Kuvan Net Product Revenue Unchanged $112 to $120
Aldurazyme Net Product Revenue to BioMarin Unchanged $79 to $83
Firdapse Net Product Revenue Unchanged $14 to $18
Selected Income Statement Guidance ($ in millions)
Item 2011 Guidance Previous 2011 Guidance
Cost of Sales (% of Total Revenue) Unchanged 18% to 20%
Selling, General and Admin. Expense Unchanged $164 to $174
Research and Development Expense Unchanged $195 to $205
Amortization and Contingent Consideration Unchanged $15
Interest Income Unchanged $3
Income Tax Expense (Benefit) Unchanged $15
GAAP Net Income (Loss) $(52) to $(42) $(60) to $(48)
Stock Compensation Expense Unchanged $43
Non-GAAP Adjusted EBITDA $51 to $61 $43 to $55
Anticipated Upcoming Milestones
2Q 2011: Initiation of pivotal Phase III trial for Firdapse for LEMS in the U.S. 3Q 2011: Top-line results from Phase II trial for PEG-PAL, including daily dosing and formulation studies 1Q 2012: Initiation of Phase III trial for PEG-PAL 1Q 2012: Initiation of Phase I trial for BMN-111 for Achondroplasia 1H 2012: 510k approval and commercial availability of the handheld blood Phe monitor for PKU 2H 2012: Top-line results for Phase III trial for GALNS for MPS IVA 2H 2012: Top-line results for PKU-016 Kuvan neurocognitive study 2H 2012: Top-line results for Phase I/II trial for BMN-701 for Pompe disease 4Q 2012/1Q 2013: Market authorization application filings for GALNS for MPS IVA
Research and Development Programs
BioMarin continues to make significant investments in research and development to ensure persistent growth of the company. The current pipeline includes programs in various stages of development that are focused on treating a range of serious unmet medical needs.
Advanced Clinical Programs
Mid-Stage Clinical Programs
Early-Stage Clinical Programs
Preclinical Programs
Non-GAAP Financial Information and Reconciliation
The above results for the three months ended March 31, 2011 and March 31, 2010 and financial guidance for the year ending December 31, 2011 are presented both as determined in accordance with GAAP and on a non-GAAP basis. As used in this release, non-GAAP income is based on GAAP Earnings Before Interest, Taxes, Depreciation and Amortization (EBITDA) adjusted to exclude non-cash stock compensation expense, contingent consideration expense and certain nonrecurring material items (adjusted EBITDA).
The following tables detail the reconciliation of non-GAAP to GAAP financial metrics:
Reconciliation of GAAP Net Income (Loss) to Non-GAAP Adjusted EBITDA
(in millions)
(unaudited)
Three Months Ended March 31, Year Ending December 31, 2011
NOTES 2011 2010 Guidance
GAAP Net Income (Loss) $ (4.4) $ 1.2 $(52) - $(42)
Interest expense, net 1.4 1.2 6
Income tax expense 4.8 0.6 15
Depreciation 4.7 3.4 24
Amortization 0.9 0.1 4
EBITDA (Loss) 7.4 6.5 (3) - 7
Stock-based compensation 10.4 8.5 43
Gain on sale of equity investments - (0.9) -
Contingent consideration (1) (0.5) 0.7 11
Adjusted EBITDA $ 17.3 $ 14.8 $51 - $61
(1) Represents the changes in the fair value of contingent acquisition consideration payable for the period.
BioMarin believes that this non-GAAP information is useful to investors, taken in conjunction with BioMarin's GAAP information because it provides additional information regarding the performance of BioMarin's core ongoing business, Naglazyme, Kuvan, Aldurazyme and Firdapse and development of its pipeline. By providing information about both the overall GAAP financial performance and the non-GAAP measures that focus on continuing operations, the company believes that the additional information enhances investors' overall understanding of the company's business and prospects for the future. Further, the company uses both the GAAP and the non-GAAP results and expectations internally for its operating, budgeting and financial planning purposes and uses the adjusted EBITDA methodology in establishing corporate goals for internal compensation programs.
Diluted Earnings Per Share Calculation
As of March 31, 2011 and March 31, 2010 , the shares related to our outstanding convertible debt are 19.1 million and 26.3 million, respectively. The calculation of non-GAAP adjusted EBITDA diluted earnings per share for the quarter ended March 31, 2011 and March 31, 2010 includes the 19.1 million shares and the 10.3 million shares, respectively, related to the company's convertible debt, as their impact is considered dilutive.
Conference Call Details
BioMarin will host a conference call and webcast to discuss first quarter 2011 financial results today, Thursday, April 28 , at 5:00 p.m. ET . This event can be accessed on the investor section of the BioMarin website at www.BMRN.com .
Date: April 28, 2011 Time: 5:00 p.m. ET U.S. / Canada Dial-in Number: 888.396.2386 International Dial-in Number: 617.847.8712 Participant Code: 42725170 Replay Dial-in Number: 888.286.8010 Replay International Dial-in Number: 617.801.6888 Replay Code: 56138656
BioMarin develops and commercializes innovative biopharmaceuticals for serious diseases and medical conditions. The company's product portfolio comprises four approved products and multiple clinical and pre-clinical product candidates. Approved products include Naglazyme® (galsulfase) for mucopolysaccharidosis VI (MPS VI), a product wholly developed and commercialized by BioMarin; Aldurazyme® (laronidase) for mucopolysaccharidosis I (MPS I), a product which BioMarin developed through a 50/50 joint venture with Genzyme Corporation; Kuvan® (sapropterin dihydrochloride) Tablets, for phenylketonuria (PKU), developed in partnership with Merck Serono, a division of Merck KGaA of Darmstadt, Germany ; and Firdapse™ (amifampridine), which has been approved by the European Commission for the treatment of Lambert Eaton Myasthenic Syndrome (LEMS). Product candidates include GALNS (N-acetylgalactosamine 6-sulfatase), which is currently in Phase III clinical development for the treatment of MPS IVA, PEG-PAL (PEGylated recombinant phenylalanine ammonia lyase), which is currently in Phase II clinical development for the treatment of PKU, BMN-701, a novel fusion protein of insulin-like growth factor 2 and acid alpha glucosidase (IGF2-GAA), which is currently in Phase I/II clinical development for the treatment of Pompe disease, and BMN-673, a poly ADP-ribose polymerase (PARP) inhibitor, which is currently in Phase I/II clinical development for the treatment of genetically-defined cancers. For additional information, please visit www.BMRN.com . Information on BioMarin's website is not incorporated by reference into this press release.
Forward-Looking Statement
BioMarin®, Naglazyme®, Kuvan® and Firdapse™ are registered trademarks of BioMarin Pharmaceutical Inc.
Aldurazyme® is a registered trademark of BioMarin/Genzyme LLC.
Contact:
Investors Media
Eugenia Shen Bob Purcell
BioMarin Pharmaceutical Inc. BioMarin Pharmaceutical Inc.
(415) 506-6570 (415) 506-3267
BIOMARIN PHARMACEUTICAL INC. CONSOLIDATED BALANCE SHEETS March 31, 2011 and 2010 (In thousands of U. S. dollars, except share and per share amounts)
March 31, 2011 December 31, 2010 (1)
ASSETS (unaudited)
Current assets:
Cash and cash equivalents $ 90,782 $ 88,079
Short-term investments 161,799 186,033
Accounts receivable, net (allowance for doubtful accounts $969 and $63, respectively) 106,198 86,576
Inventory 110,067 109,698
Other current assets 34,984 33,874
Total current assets 503,830 504,260
Investment in BioMarin/Genzyme LLC 1,133 1,082
Long-term investments 141,378 128,171
Property, plant and equipment, net 217,884 221,866
Intangible assets, net 102,692 103,648
Goodwill 53,055 53,364
Long-term deferred tax assets 231,947 236,017
Other assets 12,227 14,215
Total assets $ 1,264,146 $ 1,262,623
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable and accrued liabilities $ 75,986 $ 83,844
Total current liabilities 75,986 83,844
Convertible debt 377,521 377,521
Other long-term liabilities 89,799 84,001
Total liabilities 543,306 545,366
Stockholders' equity:
Common stock, $0.001 par value: 250,000,000 shares authorized at March 31, 2011 and December 31, 2010 : 110,873,519 and 110,634,465 shares issued and outstanding at March 31, 2011 and December 31, 2010, respectively 111 111
Additional paid-in capital 1,103,885 1,090,188
Company common stock held by Nonqualified Deferred Compensation Plan (1,733) (1,965)
Accumulated other comprehensive income (loss) (5,787) 188
Accumulated deficit (375,636) (371,265)
Total stockholders' equity 720,840 717,257
Total liabilities and stockholders' equity $ 1,264,146 $ 1,262,623
BIOMARIN PHARMACEUTICAL INC. CONSOLIDATED STATEMENTS OF OPERATIONS For the Three Months Ended March 31, 2011 and 2010 (In thousands, except for per share data)
2011 2010
REVENUES: (unaudited) (unaudited)
Net product revenues $ 109,076 $ 84,073
Collaborative agreement revenues 125 201
Royalty and license revenues 255 679
Total revenues 109,456 84,953
OPERATING EXPENSES:
Cost of sales (excludes amortization of developed product technology) 20,796 17,412
Research and development 45,017 30,097
Selling, general and administrative 41,037 34,000
Intangible asset amortization and contingent consideration 312 654
Total operating expenses 107,162 82,163
INCOME FROM OPERATIONS 2,294 2,790
Equity in the loss of BioMarin/Genzyme LLC (542) (691)
Interest income 782 1,190
Interest expense (2,141) (2,429)
Net gain from sale of investments - 927
INCOME BEFORE INCOME TAXES 393 1,787
Provision for income taxes 4,764 636
NET INCOME (LOSS) $ (4,371) $ 1,151
NET INCOME (LOSS) PER SHARE, BASIC & DILUTED $ (0.04) $ 0.01
Weighted average common shares outstanding, basic 110,652 101,144
Weighted average common shares outstanding, diluted 110,743 103,720
Total stock-based compensation expense included in the Consolidated Statements of Operations is as follows:
Three Months Ended
March 31,
2011 2010
(unaudited) (unaudited)
Cost of sales $ 1,402 $ 1,028
Research and development 3,674 3,182
Selling, general and administrative 5,304 4,336
$ 10,380 $ 8,546
SOURCE BioMarin Pharmaceutical Inc.

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Last updated: Apr 28, 2011