Guest guest Posted June 4, 2006 Report Share Posted June 4, 2006 ASCO drug conference opens Friday Annual meeting on cancer treatments a premier medical event By Val Brickates Kennedy, MarketWatch Last Update: 4:16 PM ET Jun 1, 2006 BOSTON (MarketWatch) -- Cancer drug makers are gearing up for one of the biggest market moving events of the year, the annual meeting of the American Society of Clinical Oncology, or ASCO, where over 25,000 medical professionals will gather to get updated on the latest and greatest oncology treatments. Considered one of the premier medical events, ASCO provides a unique opportunity for drug developers to roll out their latest clinical results before the very people who drive their sales -- cancer specialists. The meeting opens in Atlanta on Friday, June 2, and will run through Tuesday, June 6. Unlike past years, when ASCO news was dominated by such biotechnology heavyweights as Genentech, old-line pharmaceutical firms are expected to grab headlines this year, with Bristol-Myers Squibb's Sprycel and GlaxoKline's Tykerb potentially creating the most buzz. " All-in, we believe this year's ASCO is shaping up to highlight large pharma's competitive threat to biotech in addition to the ever-present biotech/biotech competition, " said W. Baird analyst , in his brief note on the event. Here's a round up of presentations Wall Street analysts will be watching closely, especially from Big Pharma: Bristol-Myers Squibb In a highly unusual move, the FDA has decided to convene an advisory panel at ASCO this year to review Bristol-Myers market application for Sprycel, its much-anticipated therapy for CML, or chronic myelogenous leukemia. While the agency is not bound to the recommendations of its panel of experts, it generally follows them. The FDA meeting is slated for June 2, with the agency expected to make a final decision on the drug by June 28. In general, analysts believe that the committee should give Sprycel the thumbs up. " Our physician experts believe a recommendation for Sprycel is highly likely based on reasonable tolerability and excellent efficacy, " wrote analysts at Cowen & Co. of the FDA meeting. Also a potential market mover will be Bristol-Myers' June 3 presentation of additional Phase III data on Sprycel, also known as dasatinib, for CML. The drug is initially being targeted for patients with CML who don't respond well to Novartis AG's Gleevec, the current standard treatment for the disease. In particular, the market will be looking for data on how well Sprycel performs against high doses of Gleevec. On June 4, Bristol-Myers will be presenting Phase II data for another one of its oncology products, MDX-010, for advanced melanoma. According to Bank of America, Bristol-Myers is still trying to figure out whether to pursue applying for approval of the drug in combination with other cancer drugs or as a monotherapy. " We will also be closely watching any side effect data from trials, particularly immune-mediated events, " wrote the analysts. Quote Link to comment Share on other sites More sharing options...
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