Summary
Biogen Idec Inc. reported strong financial results for the second quarter of 2009, with total revenues reaching $1,093.3 million and net income of $142.8 million, or $0.49 per diluted share. This represents a 10.1% increase in revenue compared to the same period in the prior year, driven primarily by robust growth in TYSABRI sales, which generated $187.6 million, and a $64.0 million increase in AVONEX sales. Key drivers of this performance include a 27.4% year-over-year increase in TYSABRI revenues, fueled by higher patient demand in both the US and international markets, and a 12.1% increase in AVONEX revenue, primarily due to price increases in the US and increased patient demand internationally. The company also highlighted its strong liquidity position with $2,670.7 million in cash and marketable securities, providing ample resources for operations, share repurchases, and strategic investments.
Financial Highlights
53 data points| Revenue | $1.09B |
| Cost of Revenue | $90.72M |
| Gross Profit | $1.00B |
| R&D Expenses | $416.45M |
| SG&A Expenses | $220.83M |
| Operating Expenses | $870.38M |
| Operating Income | $222.91M |
| Interest Expense | $9.30M |
| Net Income | $142.80M |
| EPS (Basic) | $0.49 |
| EPS (Diluted) | $0.49 |
| Shares Outstanding (Basic) | 288.62M |
| Shares Outstanding (Diluted) | 290.36M |
Key Highlights
- 1Total revenues for Q2 2009 increased by 10.1% year-over-year to $1,093.3 million.
- 2Net income for Q2 2009 was $142.8 million, resulting in diluted EPS of $0.49.
- 3TYSABRI revenue significantly increased by 27.4% to $187.6 million, driven by global patient demand.
- 4AVONEX revenue grew by 12.1% to $591.2 million, with US sales up 19.7% primarily due to price increases.
- 5The company maintained a strong liquidity position with $2,670.7 million in cash and marketable securities as of June 30, 2009.
- 6Biogen Idec entered into a collaboration with Acorda Therapeutics for Fampridine-SR, involving a $110.0 million upfront payment.
- 7PEGylated interferon beta-1a received Fast Track designation from the FDA for relapsing MS.