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News Breaks
March 1, 2013
14:52 EDTBIIB, SHPG, BMYBiogen, Shire among targets considered by Bristol-Myers, WSJ says
Bristol-Myers Squibb (BMY) has recently studied a possible acquisition of Biogen Idec (BIIB) and previously engaged advisers to look into the acquisition of Shire (SHPG), according to The Wall Street Journal, citing people familiar with the matters. Shares of both smaller companies rose following the initial report. In afternoon trading, Biogen advanced 0.7% to $167.50, while Shire rose 1.7% to $95.28. Reference Link
News For BIIB;SHPG;BMY From The Last 14 Days
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October 15, 2014
10:48 EDTSHPGShire tanks with AbbVie calling board meeting over merger
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10:02 EDTSHPGOn The Fly: Analyst Upgrade Summary
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09:57 EDTBMYLeerink biotech analysts hold an analyst/industry conference call
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09:20 EDTSHPGOn The Fly: Pre-market Movers
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09:11 EDTSHPGShire upgraded to Buy from Fair Value at CRT Capital
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07:30 EDTSHPGAbbVie review of Shire deal an 'unwelcome surprise,' says Jefferies
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06:58 EDTSHPGAbbVie volatility elevated into reconsidering Shire merger
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06:55 EDTSHPGShire volatility elevated into AbbVie reconsidering merger recommendation
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05:34 EDTSHPGShire says AbbVie should proceed with recommended offer
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October 14, 2014
19:50 EDTSHPGShire down nearly 6% following AbbVie reconsidering merger recommendation
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19:48 EDTSHPGAbbVie board reconsidering recommendation to holders to accept Shire merger
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19:46 EDTSHPGAbbVie board reconsidering recommendation to holders to accept Shire merger
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11:23 EDTBMY, BIIBBIND Therapeutics and The Conference Forum hold a conference
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October 13, 2014
08:05 EDTBMYBristol-Myers, Pharmacyclics, Janssen announce clinical collaboration
Bristol-Myers Squibb Company (BMY), Pharmacyclics, Inc. (PCYC), and Janssen Research & Development, LLC (JNJ) announced today they have entered into a clinical trial collaboration agreement to evaluate the safety, tolerability and preliminary efficacy of Bristol-Myers Squibb’s investigational PD-1 immune checkpoint inhibitor OPDIVO in combination with IMBRUVICA, an oral Bruton's tyrosine kinase inhibitor co-developed and co-marketed by Pharmacyclics and Janssen. The Phase 1/2 study will focus on evaluating the safety and anti-tumor activity of combining OPDIVO and IMBRUVICA as a potential treatment option for patients with non-Hodgkin lymphoma, including diffuse large B-cell lymphoma, follicular lymphoma and chronic lymphocytic leukemia. Bristol-Myers Squibb has proposed the name OPDIVO, which if approved by health authorities, will serve as the trademark for the investigational drug, nivolumab. OPDIVO is part of a new class of cancer treatments known as immunotherapies, which are designed to harness the body’s own immune system in fighting cancer by targeting distinct regulatory components of the immune system. Each agent has individually shown activity against hematologic malignancies in clinical trials; pre-clinical evidence suggests OPDIVO and IMBRUVICA may have the potential for additive treatment effects in patients with hematologic malignancies. The study will be conducted by Janssen. Additional details of the collaboration were not disclosed.
07:13 EDTBMYBioFlorida to hold a conference
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October 10, 2014
10:03 EDTBMYBristol-Myers receives orphan status for melanoma treatment
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08:19 EDTBMYMedivir announces Janssen initiates enrolment in phase II IMPACT study
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October 9, 2014
05:22 EDTSHPGShire provides regulatory update on SHP 465
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October 8, 2014
08:03 EDTBMYBristol-Myers resolves outstanding U.S. litigation on efavirenz
Bristol-Myers Squibb Company says it has "successfully resolved all outstanding U.S. patent litigation relating to efavirenz, an active ingredient contained in our Sustiva -- efavirenz -- and Atripla products. Accordingly, we believe that loss of exclusivity in the U.S. for efavirenz should not occur until December 2017. Bristol-Myers Squibb remains committed to delivering our medicines and to developing new and innovative treatments to help patients prevail over serious disease. Atripla is currently the #1 prescribed U.S. regimen in its category, with over 8 million prescriptions written since its launch in 2006. Earlier this year the company submitted a new drug application to the U.S. Food and Drug Administration for a fixed-dose combination of atazanavir sulfate and cobicistat, an investigational pharmacokinetic enhancer. In addition, studies are ongoing for new treatments including an HIV-1 attachment inhibitor, an HIV-1 maturation inhibitor and an anti-PD-L1. The establishment of intellectual property rights allows Bristol-Myers Squibb to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. We will continue to defend our intellectual property rights against infringement as we remain focused on providing a deep and broad portfolio of innovative medicines to patients around the world."
07:18 EDTBMYInfectious Diseases Society of America to hold a conference
ID Week 2014 is being held in Philadelphia on October 8-12.
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