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Bristol-Myers Squibb Co. under the ticker symbol BMY. Here is some more information that we have about Bristol-Myers Squibb Co.

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Bristol-Myers Squibb Co.


Bristol-Myers Squibb Company (BMS) engages in the discovery, development, licensing, manufacture, marketing, distribution, and sale of pharmaceuticals and nutritional products worldwide. It operates in two segments, Pharmaceuticals and Nutritionals. The Pharmaceuticals segment offers cardiovascular products, including PLAVIX, AVAPRO/AVALIDE, and PRAVACHOL; virology products comprising REYATAZ, SUSTIVA, and BARACLUDE; oncology products comprising ERBITUX, TAXOL, SPRYCEL, and IXEMPRA; affective and other psychiatric disorder products, such as ABILIFY; immunoscience products comprising ORENCIA; and other pharmaceutical products that include EFFERALGAN, ASPIRINE UPSA, DAFALGAN, and FERVEX. It sells its pharmaceutical products to wholesalers, distributors, retailers, hospitals, clinics, government agencies, and pharmacies. The Nutritionals segment manufactures, markets, distributes, and sells infant formulas and other nutritional products comprising ENFAMIL products that contain nutrients, such as docosahexaenoic and arachidonic acids. The company is also developing various compounds, which are in phase III clinical trials, including Apixaban, Saxagliptin, Dapagliflozin, Ipilimumab, Belatacept, XL-184, Tanespimycin, and Brivanib. In addition, it develops a therapeutic class of biologics called ADNECTINS. BMS has agreements with Sanofi-Aventis; Otsuka Pharmaceutical Co., Ltd.; ImClone Systems Incorporated; Gilead Sciences, Inc.; Medarex, Inc.; and AstraZeneca PLC, as well as collaborations with Pfizer Inc.; Exelixis, Inc.; and KineMed Inc. It also has an agreement with PDL BioPharma, Inc. for the development and commercialization of anti-CS1 antibody and elotuzumab for multiple myeloma; and a strategic alliance with Ensemble Discovery Corporation. The company was formerly known as Bristol-Myers Company and changed its name to Bristol-Myers Squibb Company in 1989. Bristol-Myers Squibb Company was founded in 1887 and is headquartered in New York, New York.
28,000 Employees
Last Reported Date: 02/14/14
Founded in 1887
Last $58.52 USD
Change Today -0.35 / -0.59%
Volume 5.8M
As of 4:15 PM 11/25/14 All times are local (Market data is delayed by at least 15 minutes).

bristol-myers squibb co (BMY) Snapshot

Open
$58.82
Previous Close
$58.87
Day High
$58.86
Day Low
$58.09
52 Week High
11/21/14 - $59.50
52 Week Low
06/5/14 - $46.30
Market Cap
97.1B
Average Volume 10 Days
5.3M
EPS TTM
$1.70
Shares Outstanding
1.7B
EX-Date
10/1/14
P/E TM
34.5x
Dividend
$1.44
Dividend Yield
2.46%
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BMY:US Advanced Stock Chart

bristol-myers squibb co (BMY) Related Bloomberg News

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bristol-myers squibb co (BMY) Key Developments

Bristol-Myers Squibb Company, Five Prime Therapeutics to Evaluate Investigational Immunotherapies in Six Tumor Types

Bristol-Myers Squibb Company and Five Prime Therapeutics said they have agreed to evaluate Bristol's Opdivo in combination with Five Prime's FPA008 in five different tumor types. Under the terms of the agreement, Bristol-Myers Squibb will make a one-time payment of $30 million to Five Prime Therapeutics, and will be responsible for study costs. Five Prime will conduct the clinical trial, which is expected to begin in 2015. The clinical collaboration with evaluate the safety tolerability and preliminary efficacy of combining Opdivo (nivolumab), an investigational PD-1 (programmed death-1) immune checkpoint inhibitor, with FPA008, a monoclonal antibody that inhibits colony stimulating factor-1 receptor. The combination will be evaluated in patients with non-small cell lung cancer, melanoma, head and neck cancer, pancreatic cancer, colorectal cancer and malignant glioma. Bristol-Myers Squibb has proposed the name Opdivo, which, if approved by health authorities, will serve as the trademark for nivolumab.

Bristol-Myers Announces Favorable Data from Hepatitis C Virus Trial

Bristol-Myers Squibb Company has announced favorable data from the UNITY Trial program investigating a 12-week regimen of its all-oral daclatasvir, or DCV, TRIO regimen, a fixed-dose combination of daclatasvir with asunaprevir, or ASV, and beclabuvir, or BCV, in patients with genotype 1 hepatitis C virus, or HCV. The primary endpoint for both studies was the percentage of patients who achieved cure, defined as HCV RNA. The open-label UNITY-1 study evaluated a 12-week regimen of the DCV-TRIO without ribavirin in treatment-naive and -experienced non-cirrhotic patients. Non-cirrhotic treatment-naive patients (n=312) and treatment-experienced patients (n=103) received the DCV-TRIO fixed-dose combination in one pill twice daily for 12 weeks, with 24 weeks of follow-up. The majority of the patients (73%) were genotype 1a, and 91% of all patients achieved SVR12. 92% of treatment-naive patients and 89% of treatment-experienced patients achieved cure, without the use of ribavirin. In the UNITY-2 study, both cirrhotic treatment-naive and treatment-experienced patients received the DCV-TRIO fixed-dose combination, one arm without ribavirin (n=102) and one with ribavirin (n=100). The study was double-blinded to ribavirin, and the majority of the patients (74%) were genotype 1a. The study showed 96% of all patients who received the DCV-TRIO with ribavirin achieved SVR12, and 90% of those who received the DCV-TRIO without ribavirin achieved SVR12.

Portola, Bristol-Myers Squibb and Pfizer Announce Statistically Significant Results From the First Part of the Phase 3 ANNEXA

Portola Pharmaceuticals, Inc., Bristol-Myers Squibb Company and Pfizer Inc. announced results from the first part of the Phase 3 ANNEXA(TM)-A (Andexanet Alfa a Novel Antidote to the Anticoagulant Effects of fXA Inhibitors -- Apixaban) studies. Andexanet alfa produced rapid and nearly complete reversal (by approximately 94%, p value < 0.0001) of the anticoagulant effect of Eliquis (apixaban) in healthy volunteers ages 50-75. This first part of the Phase 3 ANNEXA-A trial achieved all of its primary and secondary endpoints with statistical significance (p value>< 0.0001). The trial included 33 subjects, with 24 randomized to andexanet alfa and nine to placebo. In the study, two to five minutes after completion of a bolus dose of andexanet alfa, the anticoagulant activity of Eliquis was reversed by approximately 94% (p value>< 0.0001) compared with placebo as measured by anti-Factor Xa activity. Every subject treated with andexanet alfa had between 90 and 96% reversal of the anticoagulant activity of Eliquis. The reversal of anti-Factor Xa activity correlated with a significant reduction in the level of free, unbound Eliquis in the plasma, consistent with the mechanism of action of andexanet alfa. Additionally, andexanet alfa restored thrombin generation to baseline normal levels (prior to Eliquis therapy). In this study, no serious adverse events, thrombotic events, or antibodies to Factor X or Xa were reported following andexanet alfa administration. Mild infusion reaction was reported in three subjects>

 

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BMY:US $58.52 USD -0.35

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Industry Analysis

BMY

Industry Average

Valuation BMY Industry Range
Price/Earnings 36.2x
Price/Sales 6.1x
Price/Book 6.4x
Price/Cash Flow 35.9x
TEV/Sales 5.1x
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Bristol-Myers Squibb’s ZymoGenetics R&D Facility Earns LEED Silver Certification from U.S. Green Building Council
[at noodls] - Since its founding 100 years ago, the historic Lake Union Steam Plant, now home to Bristol-Myers Squibb's ZymoGenetics R&D subsidiary, has been a symbol of economic and civic importance to the Eastlake ...
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