News Breaks |
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| November 2, 2012 |
| 05:02 EDT |  | BMY | Bristol-Myers receives positive decision from NICE for Yervoy Bristol-Myers Squibb announced that the National Institute of Health and Clinical Excellence, or NICE, has decided to recommend Yervoy, or ipilimumab, which is approved in the European Union for the treatment of previously-treated metastatic advanced melanoma, within the Final Appraisal Determination, or FAD. This important decision will enable eligible patients in England and Wales to routinely access treatment with Yervoy through the National Health Services, or NHS. The NICE approval follows the provision of access to treatment with Yervoy for previously-treated advanced melanoma patients in an increasing number of European countries, including Spain, Germany, Austria, Switzerland, Denmark, Luxembourg, Belgium, Finland, Netherlands, Ireland and Sweden. Bristol-Myers Squibb is working closely with other European authorities to secure further access to Yervoy to address the unmet need. |
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News For BMY From The Last 14 Days Check below for free stories on BMY the last two weeks. |
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| May 17, 2013 |
| 13:21 EDT |  | BMY | Options with increasing implied volatility: CPRT BMY GDI HNZ
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| May 16, 2013 |
| 16:32 EDT |  | BMY | Bristol-Myers announces intention to voluntarily delist preferred stock
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| 13:20 EDT |  | BMY | Follow-up: Bristol-Myers upgraded to Outperform from Market Perform at Leerink Leerink upgraded Bristol-Myers citing the company's multi-billion dollar immuno-oncology prospects. The firm says there were additional responses reported in the press briefing with combination nivolumab and Yervoy. Leerink has a $51 price target for shares. |
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| 13:14 EDT |  | BMY | Bristol-Myers upgraded to Outperform from Market Perform at Leerink
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| 08:55 EDT |  | BMY | BofA/Merrill's pharmaceuticals analysts hold analyst/industry conference call
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| 08:38 EDT |  | BMY | Bristol-Myers shares likely to give back recent gains, says Leerink Leerink expects shares of Bristol-Myers to give back recent gains after ASCO published abstracts last night. The firm found the abstracts as in-line with, but not above, its expectations for nivolumab alone or immuno-oncology combination therapy and keeps a Market Perform rating on Bristol-Myers. |
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| 05:52 EDT |  | BMY | Stocks with implied volatility movement; BMY SLV
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| May 15, 2013 |
| 11:28 EDT |  | BMY | Options with increasing implied volatility: BMY AGNC EBIX IAU
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| 09:43 EDT |  | BMY | Active equity option families trading on open
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| May 14, 2013 |
| 07:24 EDT |  | BMY | EBD Group to host a conference BioTrinity 2013 is being held in Newbury, England on May 14-16. |
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| May 10, 2013 |
| 11:48 EDT |  | BMY | Drugmakers to face pressure on U.S. prices, Reuters says
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| May 9, 2013 |
| 10:17 EDT |  | BMY | Shire trades higher in London amid takeover chatter, Guardian says
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| May 8, 2013 |
| 10:33 EDT |  | BMY | Bristol-Myers, Pfizer announced results from ARISTOTLE trial subanalysis Bristol-Myers (BMY) and Pfizer (PFE) announced yesterday that results from a prespecified subanalysis of the ARISTOTLE trial were published in Circulation, the peer-reviewed journal of the American Heart Association. Results from the subanalysis showed that the reductions in stroke or systemic embolism, number of major bleeding events and mortality demonstrated with Eliquis compared to warfarin in the ARISTOTLE trial were consistent across subgroups defined based on levels of International Normalized Ratio control in patients with nonvalvular atrial fibrillation. This story corrects a headline from yesterday. |
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| May 6, 2013 |
| 17:03 EDT |  | BMY | Bristol-Myers, Pfizer announce publication of ARISTOTLE trial Bristol-Myers Squibb (BMY) and Pfizer (PFE) announced that results from a prespecified subanalysis of the ARISTOTLE trial were published in Circulation, the peer-reviewed journal of the American Heart Association. Results from this subanalysis showed that the reductions in stroke or systemic embolism, number of major bleeding events and mortality demonstrated with Eliquis compared to warfarin in the ARISTOTLE trial were consistent across subgroups defined based on levels of International Normalized Ratio control in patients with nonvalvular atrial fibrillation. Based on the results of the subanalysis, the benefits of Eliquis compared with warfarin for stroke or systemic embolism, bleeding, and mortality appear similar across the range of centers' and patients' quality of INR control. |
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| 08:53 EDT |  | BMY | BofA/Merrill's major pharma analysts hold an analyst/industry conference call
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| 07:27 EDT |  | BMY | Bristol-Myers, AstraZeneca announces results of metreleptin study
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