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Incyte Corporation at Bank of America Merrill Lynch Health Care Conference (Replay)
05/15/12 at 2:20 p.m. PT
Incyte Corporation at Bank of America Merrill Lynch Health Care Conference
Tuesday, May 15, 2012 2:20 p.m. PT  
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INCY (Common)
Exchange   NASDAQ Change   + 0.95 (4.18%)
Price   $23.70 Volume  2,094,895
Last Trade   May 16, 2012 | 4:00 p.m. ET

Corporate Profile

Incyte's vision is to become a leading drug discovery and development company by building a proprietary product pipeline of novel small molecule drugs. We have an experienced team with prior success in bringing important new drugs to market. We believe we have the resources, experience and drive to improve the lives of patients and build sustainable value for our shareholders.


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DateTitle 
May 01, 2012Incyte to Present at the Bank of America Merrill Lynch 2012 Health Care Conference
WILMINGTON, Del., May 01, 2012 (BUSINESS WIRE) --Incyte Corporation (Nasdaq: INCY) announced today it will present at the Bank of America Merrill Lynch 2012 Health Care Conference on Tuesday, May 15, 2012 at 11:20 a.m. (PT) / 2:20 p.m. (ET) in Las Vegas. The presentation will be webcast live and can be accessed at www.incyte.com under Investor Relations, Events and Webcasts. A replay of the presentation will be available for 90 days. Investors interested in ... 
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April 26, 2012Incyte Reports 2012 First-Quarter Financial Results; Updates Shareholders on Commercial Activity and Key Clinical Programs
$19.3 million in first-quarter net product revenue from JakafiTM (ruxolitinib); $25.1 million of Jakafi shipped to specialty pharmacies during the quarter Phase III studies of Jakafi published in The New England Journal of Medicine demonstrate significant clinical benefit for patients with myelofibrosis Conference Call Scheduled Today at 8:30 a.m. ET WILMINGTON, Del., Apr 26, ... 
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April 20, 2012Incyte Announces EU Regulatory Milestone for Ruxolitinib
WILMINGTON, Del., Apr 20, 2012 (BUSINESS WIRE) --Incyte Corporation (Nasdaq: INCY) announced today a European Union (EU) regulatory milestone from Novartis. The milestone includes a $40 million payment earned based on the recommendation by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) for approval of ruxolitinib for the treatment of disease-related splenomegaly or symptoms in adult patients with primary ... 
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