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News Breaks
December 31, 2012
06:13 EDTBMYBristol-Myers upgraded to Neutral from Underweight at Atlantic Equities
Atlantic Equities upgraded Bristol-Myers citing FDA approval of it anti-clotting drug, Eliquis. Price target is $32.50.
News For BMY From The Last 14 Days
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June 19, 2013
05:43 EDTBMYAstraZeneca, Bristol-Myers announce top line results of Phase 4 trial of Onglyza
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June 17, 2013
07:28 EDTBMYCambridge Healthtech Institute to host a conference
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June 14, 2013
09:03 EDTBMYBristol-Myers, AstraZeneca to present 33 abstracts at ADA Scientific Sessions
AstraZeneca (AZN) and Bristol-Myers Squibb (BMY) announced that 33 abstracts on the companies’ research in diabetes have been accepted for presentation at the 73rd Scientific Sessions of the American Diabetes Association in Chicago, June 21-25. The data include studies from five marketed products as well as dapagliflozin, an investigational compound in the U.S., currently approved for use in the European Union, Australia, New Zealand and Mexico. Key presentations include: the first presentation of Phase IIa pilot data exploring the use of dapagliflozin in adult patients with type 1 diabetes; four-year data examining the durability of dapagliflozin vs. glipizide as add-on therapies in patients with type 2 diabetes inadequately controlled on metformin; study evaluating the efficacy and tolerability of saxagliptin in patients with type 2 diabetes and a history of cardiovascular disease; three-year data from a study examining the effect of exenatide once weekly on sustained glycemic control and weight compared with insulin glargine; and Phase IV study examining glycemic control, weight, and hypoglycemia with exenatide compared to mealtime administration of rapid-acting analog insulin.
08:02 EDTBMYBristol-Myers, Simcere enter Orencia pact for China
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June 13, 2013
11:02 EDTBMYLeerink's major pharma analyst holds an analyst/Industry conference call
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June 12, 2013
13:15 EDTBMYBristol-Myers, AstraZeneca issue statement on review of some therapies
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June 11, 2013
18:09 EDTBMYOrencia trial data shows efficacy rate comparable to Humira
Bristol-Myers announced the results of year two data from AMPLE, a trial of 646 patients comparing the subcutaneous formulation of Orencia, or abatacept, vs. Humira, or adalimumab, each on a background of MTX, in biologic naïve patients with moderate to severe RA. The AMPLE year two data are being presented this week at the European League Against Rheumatism annual congress and highlighted during a congress press conference. AMPLE met its primary endpoint as measured by non-inferiority of ACR20 at year one. The Orenica regimen achieved comparable rates of efficacy vs. the Humira regimen, or 64.8% vs. 63.4%, respectively. Onset of response was also generally similar for the two groups. Year two of the study remained investigator-blinded. At year two, the Orencia regimen achieved the same rate of efficacy as the Humira regimen based on ACR20.
08:01 EDTBMYLeerink's major pharma and biotech analysts hold a conference call
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June 7, 2013
13:49 EDTBMYBristol-Myers volatility elevated as shares pullback from 11-year high
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June 6, 2013
11:04 EDTBMYBristol-Myers says Health Canada expands Abilify indications
Abilify has received an additional approval from Health Canada as an adjunct, or add-on, treatment to antidepressants for the treatment of major depressive disorder in adults who had an inadequate response to prior antidepressant treatments during the current episode.

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