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Bristol-Myers Squibb Co. (BMY) Stock Summary:

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 $49.12 USD
Change Today +0.70 / 1.45%
Volume 7.5M
As of 8:04 PM 07/18/14 All times are local (Market data is delayed by at least 15 minutes).

bristol-myers squibb co (BMY) Snapshot

Open
$48.50
Previous Close
$48.42
Day High
$49.19
Day Low
$48.28
52 Week High
03/6/14 - $57.49
52 Week Low
08/22/13 - $41.11
Market Cap
81.4B
Average Volume 10 Days
6.2M
EPS TTM
$1.76
Shares Outstanding
1.7B
EX-Date
07/1/14
P/E TM
27.9x
Dividend
$1.44
Dividend Yield
2.91%
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BMY:US Advanced Stock Chart

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bristol-myers squibb co (BMY) Key Developments

Bristol-Myers Squibb and Pfizer Announce Enrollment of First Patient in Phase IV EMANATE Trial to Assess Effectiveness and Safety of Eliquis(R) (apixaban) in Patients with NVAF Undergoing Cardioversion

Bristol-Myers Squibb Company and Pfizer Inc. announced that the first patient has been enrolled into a Phase IV clinical trial called EMANATE (Eliquis evaluated in acute cardioversion coMpared to usuAl treatmeNts for AnTicoagulation in subjEcts with NVAF) assessing the effectiveness and safety of Eliquis in patients with nonvalvular atrial fibrillation (NVAF) undergoing cardioversion. Eliquis is currently approved to reduce the risk of stroke and systemic embolism in patients with NVAF. Cardioversion (administered through electric shock to the chest or with medication) is a commonly used, effective method of converting atrial fibrillation to a normal rhythm, allowing the heart to pump more effectively. Traditionally, anticoagulation is administered for a minimum of three weeks prior to cardioversion and for four weeks afterward. In some patients, early cardioversion can be performed on the same day or within days of new-onset NVAF, usually after imaging, to confirm the absence of a pre-existing thrombus in the heart, which could be dislodged during the cardioversion procedure and cause a stroke. EMANATE, a randomized, open-label clinical trial, will assess the effectiveness and safety of Eliquis compared with usual care (parenteral heparin and/or oral anticoagulation with a vitamin K antagonist) initiated in patients with NVAF expected to undergo cardioversion after short-term anticoagulation, in a clinical practice setting. In NVAF patients presenting at least 48 hours after the onset of NVAF, early cardioversion will be performed after excluding a thrombus by imaging, on the same day or within a few days. In NVAF patients presenting within 48 hours of the onset of NVAF, cardioversion will be performed promptly without prior imaging. In all patients, Eliquis or usual care will be initiated prior to cardioversion and continued for up to 30 days post-cardioversion. The EMANATE trial is anticipated to enroll 1,500 eligible patients from the U.S., Canada, Europe and Asia. Patients will be randomized 1:1 to Eliquis or usual care, to be administered for up to 30 days following early cardioversion or 90 days post randomization if cardioversion is not performed within this timeframe. The primary efficacy endpoints are the occurrence of acute stroke, systemic embolism and all-cause death. Primary safety endpoints are major bleeding and clinically relevant non-major bleeding. ELIQUIS is indicated to reduce the risk of stroke and systemic embolism in patients with nonvalvular atrial fibrillation. ELIQUIS is indicated for the prophylaxis of deep vein thrombosis (DVT), which may lead to pulmonary embolism (PE), in patients who have undergone hip or knee replacement surgery.

Bristol-Myers Squibb Announces Plans for Third Quarter Submission of Biologics License Application for Opdivo

Bristol-Myers Squibb Company announced that, following discussions with the U.S. Food and Drug Administration (FDA), the company is planning a third quarter submission of a Biologics Licensing Application (BLA) for Opdivo(R) (nivolumab) for previously treated advanced melanoma. This will mark the second tumor type for which Bristol-Myers Squibb has a regulatory submission underway for Opdivo in the U.S. The advanced melanoma BLA is based on data from Checkmate -037, a multinational, multicenter, randomized open-label Phase 3 trial evaluating Opdivo compared to dacarbazine (DTIC) or carboplatin/paclitaxel in patients with unresectable or metastatic melanoma who have been previously treated with Yervoy(R) (ipilimumab) and, if BRAF-mutation positive, a BRAF inhibitor regimen. Bristol-Myers Squibb has proposed the name Opdivo (pronounced op-dee-voh), which, if approved by health authorities, will serve as the trade name for nivolumab. Cancer cells may exploit 'regulatory' pathways, such as checkpoint pathways, to hide from the immune system and shield the tumor from immune attack. Opdivo is an investigational, fully-human PD-1 immune checkpoint inhibitor that binds to the checkpoint receptor PD-1 (programmed death-1) expressed on activated T-cells. Investigating whether by blocking this pathway, Opdivo would enable the immune system to resume its ability to recognize, attack and destroy cancer cells. Bristol-Myers Squibb has a broad, global development program to study Opdivo in multiple tumor types consisting of more than 35 trials-as monotherapy or in combination with other therapies-in which more than 7,000 patients have been enrolled worldwide. Among these are several potentially registrational trials in non-small cell lung cancer (NSCLC), melanoma, renal cell carcinoma (RCC), head and neck cancer, glioblastoma and non-Hodgkin lymphoma.

Zafgen, Inc. Appoints Patrick Loustau as its President

Zafgen Inc. has appointed Patrick Loustau as its President. Most recently, he was the Senior Vice President for Global Commercialization (Cardiovascular & Metabolics) at Bristol-Myers Squibb Co.

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BMY

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Valuation BMY Industry Range
Price/Earnings 28.3x
Price/Sales 5.0x
Price/Book 5.3x
Price/Cash Flow 28.2x
TEV/Sales 4.1x
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Archieved Financial News About Bristol-Myers Squibb Co.

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Quote: deathsBristol-Myers Squibb Co. (BMY)’s Yervoy, cleared in March as the first treatment proven to extend lives of advanced melanoma patients. Jack ScannellLondonNew York, may earn $1.5 billion from Yervoy in 2015, according to the average estimate of three analysts surveyed by Bloomberg. Whiskey, Wine Fraud on Americans Brings 5-Year Term for Briton A British man who defrauded American and Canadian investors of about 30 million pounds ($49 million) through investment schemes tied to win...
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Roche, Daiichi Sankyo Win U.S. Approval on Drug to Treat Advanced Melanoma

Quote: deathsBaselSwitzerlandBristol-Myers Squibb Co. (BMY)’s Yervoy, cleared in March as the first treatment proven to extend lives of advanced melanoma patients. Richard Pazdur, director of the Office of Oncology Drug Products in the FDA’s Center for Drug Evaluation and Research, said in the statement. “Zelboraf is the second new cancer drug approved that demonstrates an improvement in overall survival.” Jack ScannellLondonNew York, may earn $1.5 billion from Yervoy in 201...
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U.S. FDA approves Roche skin cancer drug Zelboraf

Quote: Zelboraf was developed in partnership with Daiichi Sankyo (4568.T) and is the second drug to be approved for melanoma this year, after Yervoy from Bristol-Myers Squibb(BMY.N). Prior to 2011, the FDA had not approved a new melanoma drug in 13 years. Both are expected to top $1 billion in sales for their manufacturers, and analysts at Sanford Bernstein predict that Yervoy will capture 60 percent of the U.S. market versus 40 percent for Zelboraf. "The FDA's quick action on this drug approval is imp...
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Daiichi, Roche Win U.S. Drug Approval

Quote: In March, the FDA cleared Yervoy from Bristol-Myers Squibb Co. Unlike vemurafenib's focus on the molecular causes of metastatic melanoma, Yervoy works by marshaling the body's immune system to fight the cancer. The rival treatments are expensive, with a course of Yervoy costing $120,000. Most patients will take Zelboraf for about six months at an estimated cost of $56,400, Roche said. The genetic test identifying skin-cancer patients with the BRAF mutation will cost $120-$150, the company said. ...
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Bristol-Myers Squibb Announces the Winners of the 2011 REYATAZ® (atazanavir sulfate) “Fight HIV Your Way” Contest

Keywords: Bristol-Myers Squibb Announces the Winners of the 2011 REYATAZ® (atazanavir sulfate) “Fight HIV Your Way” Contest, bmy
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Bayer and J&J 'Muddied The Waters' With Xarelto

Quote: Meanwhile, BoehringerIngelheim has already launched Pradaxa with an aggressive promotionalcampaign and Pfizer (PFE) and Bristol-Myers Squibb (BMY) recently released studyresults that has some analysts speculating their apixaban bold thinnerwill be the one to beat (see this). The problem, according to the editorial, is that the Rocket study didnot show any superiority for Xarelto on an “intent-to-treat” basis.Instead, the study authors used a different group of patients - theas-treate...
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Cramer's Battle Plan After Wednesday's Steep Sell-Off

Quote: Specifically, Cramer stated you should wait for VZ to go to at least a 6% yield and that you should wait for a 5% yield on Bristol-Myers Squibb (BMY).Cramer discussed the difference between silver and gold, noting that gold is a purer currency while silver is also an industrial metal, and that he would prefer investors use Gold as their allocation over silver for this distinction. Cramer usually suggests that investors choose the SPDR Gold ETF (GLD) if they want to invest in gold, but also has r...
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A.M. Vitals: Genetic Immunotherapy For Leukemia Holds Promise

Quote: The treatment, to be called Complera, will join on the market another once-daily, three-drug pill intended for people new to HIV therapy — Atriplia, marketed by Gilead in conjunction with Bristol-Myers Squibb. Pet Food Threat: the New York Times’ Well blog reports. Pets can get food poisoning, and humans can get it from coming into contact with tainted pet food. Vets recommend not feeding pets raw food diets and storing dry foods, pet vitamins and treats in a cool, dry place, the NYT...
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Gilead Investors Eye Next Catalyst

Keywords: gilead sciences,hiv,aids,johnson & johnson,j&j,quad,atripla,truvada,edurant,complera,glaxosmithkline,abbott laboratories,norvir,bristol,myers squibb,integrase inhibitors,drug cocktail,viread,emtriva,MARKETS,GILD,JNJ,GSK,BMY,TEVA
Quote: Atripla, marketed with partner Bristol-Myers SquibbBMY), is the subject of a patent challenge from Teva Pharmaceutical IndustriesTEVA). Teva also is challenging Truvada’s patent. the company also announced a resolution to manufacturing problems at a California plant. The Food and Drug Administration warned the company to fix the issues last September. AIDS drugs are expensive (Complera will be sold for about $1,700 a month), and some of the pullback in Gilead’s stock is probably rela...
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FDA Submissions May Make This Bottom Bouncer More Appealing

Quote: Erbitux is marketed in the United States by Bristol-Myers Squibb Company (BMY) and Eli Lilly and Company (LLY). Merck KGaA (MRK) has the right to market Erbitux outside the US and Canada. Qiagen N.V is a provider of sample and assay technologies for life sciences, molecular diagnostics, applied testing and pharma. Its Sample technologies are used to isolate DNA, RNA, and proteins from any biological sample. The company's assay technologies are used to make specific target biomolecules, such as t...
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Qiagen: FDA Submissions May Make This Bottom Bouncer More Appealing

Quote: Erbitux is marketed in the United States by Bristol-Myers Squibb Company (BMY) and Eli Lilly and Company (LLY). Merck KGaA (MRK) has the right to market Erbitux outside the US and Canada. Qiagen N.V is a provider of sample and assay technologies for life sciences, molecular diagnostics, applied testing and pharma. Its Sample technologies are used to isolate DNA, RNA, and proteins from any biological sample. The company's assay technologies are used to make specific target biomolecules, such as t...
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AMRI cuts net loss to $568K

Quote: In the year-ago quarter, AMRI (Nasdaq: AMRI) reported a net loss of $3.9 million, or 13 cents a share. Total revenue for the second quarter was $52.4 million, a 9 percent increase from a year ago. Bristol-Myers SquibbBristol-Myers SquibbLatest from The Business JournalsGenetic testing for cholesterol drug Plavix could push Harmonyx to double revenuePlavix heart drug priced higher than local roots' rival’sBiochemical payoffFollow this company. Thomas D’Ambra, CEO of AMRI, attributed...
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Stock Market Bargains Go Begging: Cramer

Keywords: Financial, News, Stock, Market, Headlines, Investments, Quotes, Trading, TheStreet.com, Jim Cramer ,Investing Opinion
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A.M. Vitals: Alzheimer's Research Suggests Early Interventions

Quote: That’s why Pfizer, Johnson & Johnson and Bristol-Myers Squibb are looking to treat patients with signs of milder memory loss, the paper says. Hackable Devices:the Associated Press reports. Many devices contain wireless chips, but most are too small to contain encryption technology, the AP says. Lab-Grown Sperm: the WSJ reports. Experts call the research, published in Cell, a breakthrough but caution it may not translate to humans. Lower Costs: the Los Angeles Times reports. Increased u...
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Qiagen completes 2nd U.S. FDA submission of therascreen KRAS RGQ PCR Kit

Quote: by Bristol-Myers Squibb (BMY) and Eli Lilly (LLY). Merck KGaA has the right to market Erbitux outside the U.S. and Canada. QIAGEN submitted a Premarket Approval, or PMA, application to the FDA for use of its innovative assay in determining which patients can be expected to benefit from Erbitux in treatment of mCRC. PMA follows a recent submission for use with another EGFR inhibitor drug, also in patients with metastatic colorectal cancer. FDA decisions are expected in 2012. :theflyonthewall.com....
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UPDATE 3-Deutsche Post upbeat after strong Q2

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UPDATE 1-Bristol-Myers gets FDA ok for subcutaneous Orencia

Keywords: United States, CarolBishopric
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UPDATE 1-Bristol-Myers sales eclipse forecast

Keywords: United States, John Wallace
Quote: forecast of $0.55 * Raises 2011 profit view to $2.20 to $2.30/shr * Affirms 2013 forecast, representing fairly stable profit (Adds product sales, 2011, 2013 forecasts) NEW YORK, July 28 (Reuters) - Bristol-Myers Squibb Co's (BMY.N) second-quarter sales blew past Wall Street forecasts, but sharply higher taxes kept earnings roughly in line with expectations. The U.S. drugmaker on Thursday raised its 2011 profit view and reaffirmed a 2013 forecast that suggests relatively stable earnings that year...
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Quote: Ahead of the bell, drug maker Bristol-Myers Squibb (BMY) raised its 2011 profit forecast after second-quarter sales of nine of its 10 top drugs exceeded analysts’ estimates. Also, Exxon Mobil (XOM) reported its highest quarterly profit since the third-quarter of 2008. But the results fell short of Wall Street estimates. Data from the National Association of Realtors is scheduled to be released at 10 a.m. eastern time for previously owned home sales in June.......
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