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Stock Market & Financial Investment News

News Breaks
January 2, 2013
16:48 EDTMRKMerck: FDA acknowledges resubmission of NDA for Ezetimibe/Atorvastatin tablets
Merck announced that the U.S. FDA has acknowledged the resubmission of a New Drug Application for ezetimibe and atorvastatin tablets, an investigational combination medicine. The updated NDA was deemed complete for review after Merck submitted additional data in response to the FDA's Complete Response Letter issued last year. Merck expects the FDA's review to be completed in the first half of 2013. Merck is continuing to move forward with planned filings for the ezetimibe and atorvastatin combination tablet in additional countries around the world.
News For MRK From The Last 14 Days
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April 19, 2015
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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April 15, 2015
08:33 EDTMRKFDA panel results positive for Merck, says SunTrust
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April 14, 2015
13:32 EDTMRKMerck, NewLink Genetics confirm initiation of Phase 3 trial of Ebola vaccine
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April 13, 2015
08:58 EDTMRKMerck may have positive read through from briefing docs, says SunTrust
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April 9, 2015
09:25 EDTMRKPiper Jaffray pharmaceuticals analysts hold an analyst/industry conference call
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April 8, 2015
07:33 EDTMRKAdvaxis, Merck begin enrollment in Phase 1/2 of ADJX-PSA with Keytruda
Advaxis (ADXS) and Merck (MRK) announced that enrollment has initiated in the Phase 1/2 clinical trial evaluating the combination of ADXS-PSA, an investigational Lm-LLO immunotherapy, and Keytruda, the first anti-PD-1 therapy approved in the United States, in patients with previously treated, metastatic castration-resistant prostate cancer, or mCRPC. The clinical trial, KEYNOTE-046, is the first-in-human study of Advaxis's lead Lm-LLO immunotherapy candidate for prostate cancer. It is the second study initiated to evaluate the use of KEYTRUDA in the treatment of advanced prostate cancer. ADXS-PSA and KEYTRUDA are members of a class of cancer treatments known as immuno-oncology therapies. Data from preclinical studies suggest that Advaxis Lm-LLO immunotherapies in combination with a PD-1 antibody may lead to an enhanced anti-tumor immune response. The results from KEYNOTE-046 will determine the future clinical development program for the combination.
07:04 EDTMRKMerck's investigational Hep C therapy granted breakthrough therapy designations
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April 7, 2015
07:14 EDTMRKEyeforpharma to hold a summit
Philadelphia 2015 Commercial Pharma Summit is being held in Philadelphia on April 7-8.

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