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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 $49.46 USD
Change Today +0.35 / 0.71%
Volume 6.7M
As of 8:04 PM 04/17/14 All times are local (Market data is delayed by at least 15 minutes).

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bristol-myers squibb co (BMY) Key Developments

Bristol-Myers Squibb Submits New Drug Application to U.S. FDA for a Fixed-Dose Combination Tablet of Atazanavir Sulfate with Cobicistat for People Living with HIV-1

Bristol-Myers Squibb Company announced the submission of a new drug application (NDA) on April 4, 2014 to the U.S. Food and Drug Administration (FDA) for a fixed-dose combination of atazanavir sulfate, a protease inhibitor marketed as Reyataz(R), and cobicistat, an investigational pharmacokinetic enhancer, or boosting agent, that can increase the level of certain HIV-1 medicines in the blood and make them more effective. Bristol-Myers Squibb is seeking approval of the fixed-dose combination tablet for use in combination with other antiretroviral agents for the treatment of HIV-1 infection. If approved, atazanavir sulfate and cobicistat could offer patients living with HIV-1 a single tablet that eliminates the need to take a boosting agent in a separate tablet. Cobicistat is being developed by Gilead Sciences Inc. Reyataz is currently used in combination with other antiretroviral agents and is most commonly used with ritonavir, a pharmacokinetic enhancer. A once-daily therapy, Reyataz is indicated for the treatment of HIV-1 infection in treatment-naïve and treatment-experienced adult patients and pediatric patients six years of age or older. Reyataz is the only protease inhibitor that has been evaluated with cobicistat in a prospective, randomized, Phase III double-blind clinical trial (Gilead's Study 114), which compared the efficacy and safety of cobicistat-boosted Reyataz (atazanavir sulfate) versus ritonavir-boosted Reyataz in treatment-naïve adult patients for 48 weeks. Study 114 may support the clinical use of atazanavir and cobicistat together.

Bristol-Myers Squibb Extends Commercial and Distribution Deal with DKSH in Six Asian Countries

Bristol-Myers Squibb (BMS) has extended an existing relationship with DKSH in relation to the provision of services in six markets in Asia. Under the deal, DKSH will provide marketing, sales, warehousing, physical distribution, credit management, and collection services for BMS in Hong Kong, Malaysia, Singapore, Taiwan, Thailand and Vietnam.

Bristol-Myers Squibb Company Announces Phase III Results from the Global Hallmark-Dual Study

Bristol-Myers Squibb Company announced Phase III results from the global HALLMARK-Dual study investigating the all-oral, interferon- and ribavirin-free regimen of daclatasvir (DCV), a NS5A inhibitor, and asunaprevir (ASV), a NS3 inhibitor, among genotype 1b hepatitis C virus (HCV) infected patients. Results showed that the 24-week regimen achieved an overall sustained virologic response (a functional cure) 12 weeks after the end of treatment (SVR(12)) among treatment-naïve (90%), peginterferon/ribavirin non-responder (82%), and peginterferon/ribavirin ineligible/intolerant (82%) patients, including cirrhotic and non-cirrhotic patients (84% and 85%). In the study the DCV+ASV regimen was generally well tolerated. Globally, there are 170 million people infected with HCV, with genotype 1 being the most prevalent. There are 9 million people infected in Europe, where there is a high prevalence of HCV genotype 1b. These data were part of the company's recent DCV and ASV new drug application (NDA) submissions to the U.S. Food and Drug Administration (FDA), and helped support the validated marketing authorization application to the European Medicines Agency for the use of DCV in combination with other agents for the treatment of adults with HCV with compensated liver disease, including genotypes 1, 2, 3, and 4. These data are comparable to a similar Phase III study of this regimen in Japanese patients, which led to the submission of a New Drug Application with Japan's Pharmaceutical and Medical Devices Agency. This Phase III multinational clinical trial involved 116 sites in 18 countries, including countries that have a high prevalence of genotype 1b such as Korea and Taiwan. In the study, treatment-naïve patients (n=205) received DCV 60 mg once daily plus ASV 100 mg twice daily for 12 weeks, and 102 patients received matching placebo for 12 weeks. The DCV+ASV treatment-naïve group continued treatment through week 24; placebo recipients entered another DCV+ASV study. The peginterferon/ribavirin-ineligible/intolerant (n=235) and non-responder patients (n=205) received the same doses of DCV and ASV for 24 weeks. The primary endpoint was the percentage of patients with a sustained virologic response at 12 weeks after the end of treatment (SVR(12)). Virologic Response, 90% of treatment-naïve patients achieved SVR12, 82% of patients with prior null or partial response to peginterferon/ribavirin (non-responders) achieved SVR12, 82% of peginterferon/ribavirin ineligible/intolerant patients achieved SVR12, Among peginterferon/ribavirin ineligible/intolerant patients, SVR12 was achieved by patients with anemia/neutropenia (91%); depression (80%) and compensated advanced fibrosis/cirrhosis with thrombocytopenia (73%). Results among Cirrhotic Patients treated with DCV+ASV: At baseline, 33 treatment-naïve, 63 non-responders, and 111 ineligible/intolerant patients had cirrhosis. Cirrhotic patients made up 32% of the study population. SVR rates were similar in cirrhotic (84%) and non-cirrhotic (85%) patients.

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Archieved Financial News About Bristol-Myers Squibb Co.

UK's NICE backs cut-price Novartis leukaemia drug

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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,, Jim Cramer ,Investing Opinion
Quote: The futures themselves have long since ceased to be an accurate barometer of the market and are instead accurate barometers of hedge-fund allocations to the commodity.It is tremendously beneficial to the oil companies, particularly those that are refiners, to keep it that way, so they don't bring oil to the market to respond to the demand.It's a big act.But it does affect the consumer.If Standard & Poor's hadn't been like Zeus throwing thunderbolts at our markets -- and if there weren't genuine ...
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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.
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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

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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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Gold Moves Higher As Silver Slides Ahead Of Debt Ceiling Vote

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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