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Bristol Myers Squibb (BMY)

(Real Time Quote from BATS)

$44.98 USD

44.98
1,213,530

+0.16 (0.36%)

Updated Aug 7, 2025 10:36 AM ET

Zacks Rank:

This is our short term rating system that serves as a timeliness indicator for stocks over the next 1 to 3 months. How good is it? See rankings and related performance below.

Zacks Rank Definition Annualized Return
1Strong Buy23.75%
2Buy17.82%
3Hold9.58%
4Sell5.28%
5Strong Sell2.61%
S&P50011.30%

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3-Hold of 5     3    

Style Scores:

The Style Scores are a complementary set of indicators to use alongside the Zacks Rank. It allows the user to better focus on the stocks that are the best fit for his or her personal trading style.

The scores are based on the trading styles of Value, Growth, and Momentum. There's also a VGM Score ('V' for Value, 'G' for Growth and 'M' for Momentum), which combines the weighted average of the individual style scores into one score.

  • Value Score A
  • Growth Score A
  • Momentum Score A
  • VGM Score A

Within each Score, stocks are graded into five groups: A, B, C, D and F. As you might remember from your school days, an A, is better than a B; a B is better than a C; a C is better than a D; and a D is better than an F.

As an investor, you want to buy stocks with the highest probability of success. That means you want to buy stocks with a Zacks Rank #1 or #2, Strong Buy or Buy, which also has a Score of an A or a B in your personal trading style.

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A Value D Growth C Momentum C VGM

Industry Rank:

The Zacks Industry Rank assigns a rating to each of the 265 X (Expanded) Industries based on their average Zacks Rank.

An industry with a larger percentage of Zacks Rank #1's and #2's will have a better average Zacks Rank than one with a larger percentage of Zacks Rank #4's and #5's.

The industry with the best average Zacks Rank would be considered the top industry (1 out of 265), which would place it in the top 1% of Zacks Ranked Industries. The industry with the worst average Zacks Rank (265 out of 265) would place in the bottom 1%.

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Top 41% (100 out of 246)

Industry: Medical - Biomedical and Genetics

Zacks News

New York-based Bristol-Myers Squibb is a one of the leading global specialty bio-pharmaceutical companies focused on the development of treatments targeting serious diseases. Backed by its blockbuster immune-oncology drug, Opdivo, Bristol-Myers has a strong oncology portfolio, consisting of other drugs like Revlimid, Sprycel, Yervoy and Empliciti. Beyond oncology, the company has important immunology and cardiovascular drugs like Orencia and Eliquis, which diversify its portfolio. Notably, in the cardiovascular space, Eliquis is now the global leading oral anti-coagulant drug. The company continues to experience growth in both the Eliquis brand and the market, while also advancing its Factor XIa inhibitor program..

Zacks Equity Research

Bristol-Myers (BMY) Opdivo Gets Approval for Liver Cancer

Bristol-Myers Squibb Company (BMY) announced that the FDA has approved immuno-oncology drug Opdivo for liver cancer.

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    Pharma Stock Roundup: Pfizer Files Suit against J&J, Supernus Hit by Study Update

    Industry heavyweights like Pfizer (PFE) and Johnson & Johnson were in the news this week related to a lawsuit while Glaxo got FDA approval for a key drug.

      Zacks Equity Research

      Roche's (RHHBY) Tecentriq Studies Put on Partial Hold by FDA

      Roche Holdings AG (RHHBY) announced that the FDA has put a partial clinical hold on a phase Ib and phase I/II b trials evaluating immunotherapy drug Tecentriq.

        Zacks Equity Research

        Oncology Space in Focus this Week on ESMO Presentations

        There were multiple presentations at European Society for Medical Oncology 2017 Congress. AstraZeneca's lung cancer study data was positive and so was Bristol-Myers's melanoma candidate.

          Zacks Equity Research

          Bristol-Myers (BMY) Collaborates With Halozyme for ENHANZE

          Bristol-Myers Squibb Company (BMY) enters into a collaboration and license agreement with Halozyme Therapeutics, Inc. (HALO).

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            Pharma Stock Roundup: Achillion Slumps on End of HCV Deal, Teva Gets a New CEO

            Key highlights this week include Teva's (TEVA) CEO announcement and the FDA approval of the first cancer biosimilar.

              Zacks Equity Research

              Nektar (NKTR) Starts PROPEL Combo Study for Cancer Candidate

              Nektar (NKTR) initiates phase I/II combo study on lead candidate NKTR-214 along with Tecentriq and Keytruda. The trial complements Nektar's ongoing PIVOT research clubbed with Opdivo.

                Zacks Equity Research

                Bristol-Myers Reports Positive Results from Melanoma Study

                Bristol-Myers Squibb Company (BMY) announced encouraging results from a phase III study, CheckMate -238, on Opdivo.

                  Zacks Equity Research

                  Company News For Sep 12, 2017

                  Companies in the news are: TEVA,BMY,EFX,FB

                    Zacks Equity Research

                    Bristol-Myers' Opdivo Study Meets Early Success, Stock Up

                    Bristol-Myers' (BMY) phase III study evaluating Opdivo plus Yervoy successfully met its co-primary endpoints and thus was stopped earlier than expected.

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                      Pharma Stock Roundup: Lilly to Cut Jobs, Streamline Operations, NVS CEO to Step Down in 2018

                      Key highlights this week include Eli Lilly and Company's (LLY) decision to cut the work force and streamline operations and Merck's efforts to strengthen its immune-oncology franchise.

                        Zacks Equity Research

                        Bristol-Myers' (BMY) Opdivo's Myeloma Studies Put on Hold

                        Bristol-Myers Squibb Company (BMY) announced that the FDA put a partial clinical hold on three clinical trials, investigating Opdivo-based combinations in patients with relapsed or refractory multiple myeloma.

                          Zacks Equity Research

                          AbbVie Submits NDA for Endometriosis Candidate to the FDA

                          AbbVie Inc. (ABBV) and partner Neurocrine Biosciences announced that the new drug application (NDA) for their pipeline candidate, elagolix, has been submitted to the FDA.

                            Zacks Equity Research

                            4 Drug Stocks Worth a Look on Promising Cancer Pipeline

                            Cancer is the second most common cause of death in the U.S. preceded only by heart disease. We discuss four pharma giants, which possess the industry's strongest oncology pipeline portfolios.

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                              Key FDA Regulatory Events to Watch Out for in Sep 2017

                              Will the FDA follow the recommendation of its advisory panel and give its nod to Amgen (AMGN) and Mylan's biosimilars?

                                Zacks Equity Research

                                Incyte (INCY) Reports Positive Data on Epacadostat/Keytruda

                                Incyte Corporation (INCY) announced new and updated data from the ongoing phase I/II ECHO-202 trial on pipeline candidate epacadostat with Keytruda.

                                  Zacks Equity Research

                                  Pfizer's sNDA for Bosulif Accepted in the U.S. and Europe

                                  Pfizer (PFE) along with Avillion announced that the regulatory authorities in the U.S. and Europe have accepted the application for label expansion of Bosulif to include newly diagnosed patients.

                                    Zacks Equity Research

                                    Pfizer Presents Encouraging Eliquis Results in NVAF Patients

                                    Pfizer (PFE) and partner Bristol-Myers presented data on Eliquis which showed the potential of the drug in reducing stroke and systemic embolism in NVAF patients undergoing cardioversion.

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                                      Pharma Stock Roundup: Roche Drug Gets Priority Review, EU Nod for Novartis Drug

                                      It was a pretty slow week with key highlights including regulatory updates from companies like Roche (RHHBY) and Novartis.

                                        Zacks Equity Research

                                        Celldex Ends Phase II Enrollment for Breast Cancer Candidate

                                        Celldex (CLDX) announces completion of enrollment in METRIC, a phase IIb study, evaluating glembatumumab vedotin for breast cancer treatment.

                                          Zacks Equity Research

                                          Here's Why Clovis Stock Is Up Almost 60% So Far in 2017

                                          Clovis Oncology (CLVS) stock is on the rise. The company's only approved drug Rubraca is off to an impressive start and is nearing label expansion approval.

                                            Zacks Equity Research

                                            Gilead (GILD) HCV Drug Vosevi Receives Approval in Canada

                                            Gilead Sciences, Inc.'s (GILD) HCV portfolio receives a boost with the approval of Vosevi in Canada.

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                                              Pharma Stock Roundup: Multiple Sclerosis Drug Prices in Focus, Mixed Data on BMY's Opdivo

                                              Key highlights this week in the pharmaceutical sector include the launch of a drug pricing probe, a resignation from the President's manufacturing council and data on Bristol-Myers' (BMY) Opdivo.

                                                Zacks Equity Research

                                                Exelixis Submits sNDA for Kidney Cancer Drug Cabometyx

                                                Exelixis, Inc. (EXEL) submitted its supplemental New Drug Application (sNDA) to the FDA for Cabometyx tablets for patients with previously untreated kidney cancer.

                                                  Zacks Equity Research

                                                  FDA Accepts Portola's (PTLA) BLA Resubmission for AndexXa

                                                  FDA acknowledges Portola's (PTLA) resubmitted BLA for AndexXa to raise hopes for an urgent need of antidotes for Factor Xa inhibitors in the market.