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Featuresearnings

Bristol-Myers profits beat estimates as it readies new immuno-harnessing cancer drug

By
Laura Lorenzetti
Laura Lorenzetti
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By
Laura Lorenzetti
Laura Lorenzetti
Down Arrow Button Icon
July 24, 2014, 9:14 AM ET
Bristol-Myers 2013 Earnings Forecast Beats Estimates
Lamberto Andreotti, president, chief operating officer and chief executive officer designate of Bristol-Myers Squibb Co., speaks during an investor meeting in New York, U.S., on Thursday, March 4, 2010. Bristol-Myers Squibb Co. said earnings, excluding some costs, will drop to as low as $1.95 a share in 2013 from projected 2010 profit, as its top-selling drug, the blood thinner Plavix, loses patent protection. Photographer: Daniel Acker/Bloomberg via Getty ImagesBloomberg--Getty Images

Bristol-Myers Squibb (BMY) beat expectations for its second-quarter earnings, bolstered by fast growth in sales of key cancer drugs Yervoy and Sprycel.

Earnings were 48 cents a share, excluding one-time items, topping the average analyst estimate of 45 cents, according to data compiled by Bloomberg. Yervoy sales were up 38% year-over-year to $321 million globally, compared with the average analyst estimate of $292 million. Sprycel sales grew 18% over the year to $368 million, slightly shy of the analysts’ expectations. Sales of Bristol-Myers’ best-selling drug Abilify, an anti-psychotic, dipped 1% to $555 million.

The New York City-based drug-maker’s bottom line suffered from a 49% increase in research and developments costs, including impairment and acquisition-related charges of $458 million, driving net income down 37% to $333 million, to 20 cents a share on a GAAP basis, from $535 million, or 32 cents a share, a year earlier.

Those factors also led it to cut its full-year guidance for earnings under U.S. Generally Accepted Accounting Principles by 12% to a range of $1.50-$1.60. However, it kept its non-GAAP guidance unchanged. The market prefers to follow the non-GAAP measure on the view that it better reflects the earnings potential of drugs under development.

More:Bristol-Myers Squibb: Big Pharma’s small wonder

Investors are carefully watching Bristol-Myers’ development of its nivolumab drug Opdivo, a cancer therapy that uses the body’s immune system to fight off the disease. The drug was approved in Japan this month for the treatement of certain-types of melanoma, making it the first PD-1 immune checkpoint inhibitor to receive regulatory approval anywhere in the world.

Bristol-Myers is partnering with Ono Pharmaceutical, a Japanese drug maker, to bring Opdivo, Yervoy and three early-state immune-targeting cancer drugs to the Asian market, the companies announced Wednesday.

In the U.S. Market, Bristol-Myers will submit a biologics license to the Food and Drug Administration for Optivo in the third quarter to seek approval for its use in treating melanoma. This will be the second regulatory submission underway for Opdivo in the U.S. The company is also seeking approval for the drugs use in treating a specific type of lung cancer.

Opdivo’s approval would give Bristol-Myers a potent treatment, which is being tested alone and in combination with other drugs in its portfolio, that will help boost sales.

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By Laura Lorenzetti
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