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April 17, 2014
13:50 EDTMRKFDA approves Ragwitek for short ragweed pollen allergies
The Food and Drug Administration approved Ragwitek, the first allergen extract administered under the tongue to treat short ragweed pollen induced allergic rhinitis, with or without conjunctivitis, in adults 18 years through 65 years of age. Ragwitek is manufactured for a subsidiary of Merck by Catalent Pharma Solutions.
News For MRK From The Last 14 Days
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April 27, 2015
18:56 EDTMRKOn The Fly: After Hours Movers
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18:32 EDTMRKMerck announces publication of pivotal data from Zerbaxa Phase 3 clinical study
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17:13 EDTMRKMerck announces Januvia study achieved primary endpoint
Merck announced that the trial evaluating cardiovascular outcomes with Sitagliptin, or TECOS, of Merck's DPP-4 inhibitor, Januvia, or sitagliptin, achieved its primary endpoint of non-inferiority for the composite cardiovascular endpoint. Among secondary endpoints, there was no increase in hospitalization for heart failure in the sitagliptin group versus placebo. The complete results of TECOS will be presented on June 8 at the Scientific Sessions of the American Diabetes Association. TECOS was an event-driven trial conducted in adults with type 2 diabetes and a history of cardiovascular disease. The study was designed to assess the CV safety of long-term treatment with Januvia as part of usual diabetes care compared with usual care without Januvia. The primary endpoint was the composite of time to the first of any of the following confirmed events: cardiovascular-related death, nonfatal myocardial infarction, nonfatal stroke, or unstable angina requiring hospitalization. TECOS enrolled 14,724 participants from 38 countries between December 2008 and July 2012. The median patient follow-up was approximately three years.
15:04 EDTMRKNotable companies reporting before tomorrow's open
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13:43 EDTMRKEarnings Watch: Merck shares lower by about 5.6% since last earnings report
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09:37 EDTMRKBarclays healthcare analysts hold an analyst/industry conference call
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06:19 EDTMRKPharmceutical companies buy drugs and raises prices, WSJ reports
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April 24, 2015
07:58 EDTMRKMerck May weekly volatility elevated into Q1 and outlook
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05:35 EDTMRKMerck Phase 3 C-EDGE program shows high sustained virologic responses
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April 23, 2015
16:39 EDTMRKACETO subsidiary to launch Timolol Maleate Ophthalmic Solution
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05:40 EDTMRKMerck announces results from C-SURFER Phase 2/3 study
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April 22, 2015
08:18 EDTMRKOrganovo enters into a collaboration agreement with Merck Sharp and Dohme
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April 21, 2015
08:30 EDTMRKMerck reaffirms commitment to developing medicines for infectious diseases
Merck reaffirmed its longstanding commitment to discovering and developing novel medicines in the global fight against infectious diseases, including infections caused by resistant bacteria and other pathogens. At this year’s 25th European Congress of Clinical Microbiology and Infectious Diseases, April 25-28 in Copenhagen, Denmark, researchers are scheduled to present more than 30 scientific data presentations on the company’s broad portfolio of marketed and investigational anti-infective medicines. Merck completed its acquisition of Cubist Pharmaceuticals, Inc. on Jan. 21, 2015, and continues to build on both companies’ work in infectious disease. Antimicrobial research remains an important area of focus. In addition to a combined portfolio of antibiotic and antifungal medicines, vaccines, and medicines for HIV and HCV, Merck has multiple programs that span discovery through late-stage development. In total, Merck currently has more than 15 ongoing clinical trials evaluating antibiotic, antifungal and antiviral agents for the prevention and treatment of infectious disease. These trials are projected to enroll approximately 8,000 patients.
April 20, 2015
08:05 EDTMRKTetraLogic, Merck enter into oncology clinical study collaboration
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07:20 EDTMRKAmerican Association for Cancer Research to hold annual meeting
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April 19, 2015
19:35 EDTMRKMerck to swiftly repay $5B loan, explore acquisitions by late 2017, Reuters says
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15:21 EDTMRKMerck announces new data from Keytruda study
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14:59 EDTMRKMerck's Keytruda 'superior' to ipilimumab for PFS in patients with melanoma
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14:47 EDTMRKMerck submits supplemental biologics license for Keytruda in lung cancer
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14:31 EDTMRKMerck reports 28% Keytruda response rate in 25 pleural mesothelioma patients
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