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Merck To Buy Biotech Firm for $1.1 Billion


Posted on 2006-10-31 08:40:00



Pharmaceutical company Merck & Co. said Monday it agreed to pay an $1.1 billion to buy Sirna Therapeutics Inc., a tiny biotechnology firm developing drugs based on new technology at the heart of last month's Nobel Prize for medicine award.

Merck's $13-per-share offer for the San Francisco-based company is almost a 102 percent premium over Sirna's closing Nasdaq Stock Market price of $6.45, which fell 5 cents before the bid was made public after the stock markets closed. Sirna's stock surged 98 percent to $12.74 in after-hours trading. The stock's high for the past year is $8.52, set in April.

Merck's stock fell 45 cents to $45.64 at the close of trading on the New York Stock Exchange and remained unchanged in after-hours trading.

Sirna is developing drugs using so-called RNA interference technology. There are at least a half-dozen biotechnology companies developing drugs that silence genes by interfering with the messenger-carrying RNA, a technique discovered by this year's Nobel winners, Andrew Fire of Stanford University and Craig Mello at the University of Massachusetts. There are eight U.S and European patents specifically related to the technology.

Analysts said the deal could spur other similar acquisitions of some of Sirna's handful of competitors who are racing to commercialize a discovery made only eight years ago -- a short time in the scientific world.

Normally skittish venture capitalists already have invested hundreds of millions in the nascent technology and now Merck has made its second, most substantive bet on RNA interference. The Whitehouse Station, N.J.-based company previously had invested in Alnylam Pharmaceuticals, a Sirna competitor.

The closest drug Sirna has near market is for the treatment of the eye disorder, macular degeneration, a leading cause of blindness in the elderly. However, that drug is still at least two years from regulatory approval and probably further out because its experimental treatment will require the successful completion of at least two costly, time-consuming and large-scale human trials testing for safety and effectiveness.