Roche Outlook, Stock Buoyed by Avastin Approval

Mon Feb 25, 2008 6:03pm EST
 
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By Sam Cage

ZURICH (Reuters) - Analysts raised forecasts for Roche Holding AG (ROG.VX) on Monday after U.S. regulators approved its Avastin drug for treating advanced breast cancer, adding a potentially significant new revenue source.

Most observers had expected the Food and Drug Administration (FDA) either to delay a decision or reject the medicine for this use, so the news pushed Roche stock up nearly 4 percent in early trade, following 9 percent gains for its U.S. partner Genentech Inc DNA.N late on Friday.

"The market had hardly reckoned on this decision," said Zuercher Kantonalbank analyst Michael Nawrath, who reiterated an Overweight rating on Roche.

"The potential sales of 1 billion Swiss francs in 2008 had been taken out of our model. Now we are adding 5 percent to Avastin sales in 2008 and 2009," Nawrath said.

Roche participation certificates, its most widely traded form of equity, were 3.9 percent higher at 203.70 Swiss francs at 0927 GMT, while the European pharmaceuticals sector index .SXDP was up 1.3 percent.

An FDA advisory voted 5-4 against approval in December, but positive new data from a clinical study was released last week.

"We expect many on the Street will need to increase 2008 and 2009 numbers, as approval will bring better reimbursement and ability to market in breast cancer," said Andrew Baum, analyst at Morgan Stanley, who kept an "overweight" rating on the stock.

Landsbanki Kepler analyst Denise Anderson, who maintained a "buy" rating, said she would add back the 500 million francs in 2008 sales that were deleted after the panel vote.

Avastin, which works by choking off the blood supply that tumors need to grow, is expected to be one of the world's biggest selling drugs.

It is already approved in colorectal and non-small-cell lung cancers, but faces competition from several other medicines, including Erbitux from ImClone Systems Inc IMCL.O and Merck KGaA (MRCG.DE).

The drug was approved under a scheme that allows the FDA to approve medicines against life-threatening diseases based on initial positive data, and the final green light will depend on further review of data from late-stage clinical trials.

Breast cancer affects 1.2 million people a year globally and kills 500,000, according to the World Health Organization.

(Editing by Will Waterman)

 

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