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Stock Market & Financial Investment News

News Breaks
October 23, 2012
08:15 EDTMRK, SNYFDA warning on Ambien would benefit Merck, says JPMorgan
JPMorgan says the potential FDA safety warning on Sanofi's (SNY) Ambien could be positive for Merck's (MRK) insomnia treatment candidate suvorexant. The firm says its physician survey suggests such a warning would change Ambien prescribing habits and keeps an Overweight rating on shares of Merck.
News For MRK;SNY From The Last 14 Days
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May 17, 2013
08:03 EDTSNYSanofi reports positive topline results from pivotal Phase III Jakarta study
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05:18 EDTSNYSanofi says JAK2 inhibitor for myelofibrosis met primary endpoint
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May 16, 2013
08:55 EDTMRKBofA/Merrill's pharmaceuticals analysts hold analyst/industry conference call
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May 15, 2013
15:16 EDTSNYSanofi systemic sclerosis treatment designated for orphan drug status
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05:39 EDTSNYSanofi, Regeneron announce patient enrollment in two Phase 3 trials
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May 14, 2013
17:39 EDTMRKMoody's lowers Merck's guaranteed debt to A1 from Aa3; stable outlook
Moody's Investors Service lowered the long-term ratings of Merck by one notch, including the guaranteed senior unsecured rating to A1 from Aa3 and the non-guaranteed senior unsecured rating to A2 from A1. This action concludes a review for downgrade initiated on May 1, 2013. At the same time, Moody's affirmed Merck's Prime-1 commercial paper rating. The rating outlook is stable.
May 13, 2013
09:44 EDTSNYSeveral companies reportedly interested in buying Adcock Ingram, Globes says
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07:30 EDTSNYTechConnect to host a summit
2013 National Innovation Summit is being held in Washington, D.C. on May 12-16.
May 10, 2013
11:48 EDTMRK, SNYDrugmakers to face pressure on U.S. prices, Reuters says
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06:53 EDTMRKGlaxoSmithKline, Merck to discount cancer vaccine in poor nations, NY Times says
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May 9, 2013
07:22 EDTMRKMerck awarded significant portion of UNICEF HPV vaccine tender
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May 8, 2013
08:32 EDTMRKMerck says FDA accepts biologics license application for allergy tablet
Merck announced that the Biologics License Application for its investigational ragweed pollen sublingual allergy immunotherapy tablet has been accepted for review by the U.S. Food and Drug Administration. The BLA for Merck’s investigational ragweed pollen sublingual allergy immunotherapy tablet is supported by five studies evaluating the efficacy and safety of the tablet in adults, 18 years of age or older, with ragweed induced allergic rhinitis. On March 27, Merck announced that the FDA had also accepted the BLA for its investigational Timothy grass pollen sublingual allergy immunotherapy tablet. Merck expects the FDA’s review for both to be completed in the first half of 2014.
May 6, 2013
08:53 EDTMRKBofA/Merrill's major pharma analysts hold an analyst/industry conference call
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07:49 EDTSNYBernstein's global pharmaceuticals analyst has analyst/industry conference call
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07:18 EDTMRKAmerican Congress of Obstetrics and Gynecology to hold annual meeting
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