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Bristol-Myers Squibb and Infinity Pharmaceuticals Announce a New Clinical Collaboration to Evaluate Opdivo (Nivolumab) in Combination with IPI-549 in Urothelial Cancer
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Halozyme Therapeutics (HALO) Reports First Clinical Dosing In Bristol-Myers Squibb (BMY) Phase 1 Trial Of BMS-986179 With Enhanze Technology
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Halozyme Announces First Clinical Dosing In Bristol-Myers Squibb's Phase 1 Trial Of BMS-986179 With Enhanze® Technology
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Bristol-Myers Squibb Reports Third Quarter Financial Results
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Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) Results in Significantly Longer Treatment-Free Survival in Patients with Previously Untreated Advanced or Metastatic Renal Cell Carcinoma
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Bristol-Myers Squibb (BMY) Reports Data from Phase 3 CheckMate -067 Clinical Trial for Opdivo (nivolumab) in Combination with Yervoy (ipilimumab)
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Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) Demonstrates Durable Four-Year Survival Benefits in Patients with Advanced Melanoma
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Opdivo (nivolumab) Plus Low-Dose Yervoy (ipilimumab) Demonstrates Durable Clinical Benefit in Previously Untreated Patients with MSI-H or dMMR Metastatic Colorectal Cancer
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Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) Shows Promising Results in Patients with Advanced Form of Bladder Cancer
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Bristol-Myers Squibb (BMY) Provides Update on Ongoing Regulatory Review of Opdivo Plus Low-Dose Yervoy
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Bristol-Myers Squibb Provides Update on the Ongoing Regulatory Review of Opdivo Plus Low-Dose Yervoy in First-Line Lung Cancer Patients with Tumor Mutational Burden ≥10 mut/Mb
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Bristol-Myers Squibb to Showcase Immunoscience Research and Biomarker-Guided Treatment Approaches at the 2018 American College of Rheumatology and Association of Rheumatology Health Professionals Annu
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Bristol-Myers Squibb (BMY) Announces Phase 3 CheckMate -331 Study Does Not Meet Primary Endpoint of OS with Opdivo Versus Chemotherapy in Patients with Previously Treated Relapsed SCLC
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Bristol-Myers Squibb Announces Phase 3 CheckMate -331 Study Does Not Meet Primary Endpoint of Overall Survival with Opdivo Versus Chemotherapy in Patients with Previously Treated Relapsed Small Cell L
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Bristol-Myers Squibb (BMY) and Compugen (CGEN) Announce Clinical Collaboration to Evaluate Therapeutic Regimen in Advanced Solid Tumors
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Bristol-Myers Squibb and Compugen Announce Clinical Collaboration to Evaluate Therapeutic Regimen in Advanced Solid Tumors
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Bristol-Myers Squibb and Compugen Announce Clinical Collaboration to Evaluate Therapeutic Regimen in Advanced Solid Tumors
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Bristol-Myers Squibb (BMY) Announces EMA Validates its Application for Empliciti Plus Pomalidomide and Low-Dose Dexamethasone in Patients with Multiple Myeloma
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European Medicines Agency Validates Bristol-Myers Squibb’s Application for Empliciti (elotuzumab) Plus Pomalidomide and Low-Dose Dexamethasone in Patients with Multiple Myeloma
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European Medicines Agency Validates Bristol-Myers Squibb’s Application for Empliciti (elotuzumab) Plus Pomalidomide and Low-Dose Dexamethasone in Patients with Multiple Myeloma
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Natera (NTRA) Enters Agreement with Bristol-Myers (BMY) for Signatera ctDNA Assay
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Bristol-Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Reports 'Significant Skin Clearance' from Phase 2 Study of BMS-986165 in Patients with Moderate to Severe Plaque Psoriasis
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Bristol-Myers Squibb’s Novel, Oral, Selective TYK2 Inhibitor Delivered Significant Skin Clearance in Patients with Moderate to Severe Plaque Psoriasis in Phase 2 Trial
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Bristol-Myers Squibb to Take Part in Morgan Stanley Global Health Care Conference
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Bristol-Myers Squibb to Announce Results for Third Quarter 2018 on October 25
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Bristol-Myers Squibb Kicks Off Coast 2 Coast 4 Cancer Ride to Fundraise for the V Foundation for Cancer Research
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Bristol-Myers Squibb (BMY) Reports FDA Approval of Supplemental Biologics License Application for Sprycel (dasatinib) in Pediatric Patients
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U.S. Food and Drug Administration Accepts Bristol-Myers Squibb’s Application for Sprycel (dasatinib) in Pediatric Patients with Newly Diagnosed Philadelphia Chromosome-Positive Acute Lymphoblastic L
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Bristol-Myers Squibb Appoints Christopher Boerner Executive Vice President and Chief Commercial Officer
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Bristol-Myers Squibb (BMY) Says FDA Accepts for Priority Review of its Application for Empliciti Plus Pomalidomide and Low-Dose Dexamethasone in Patients with RRMM
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U.S. Food and Drug Administration Accepts for Priority Review Bristol-Myers Squibb’s Application for Empliciti (elotuzumab) Plus Pomalidomide and Low-Dose Dexamethasone in Patients with Relapsed or
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Bristol-Myers Squibb (BMY) Says FDA Approved Opdivo as First New Medication in Nearly 20 Years for Certain Patients with Previously Treated SCLC
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U.S. Food and Drug Administration Approves Opdivo® (nivolumab) as the First New Medication in Nearly 20 Years for Certain Patients with Previously Treated Small Cell Lung Cancer
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Bristol-Myers Squibb (BMY) Reports EMA Approval for Opdivo (nivolumab)
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European Commission Approves Bristol-Myers Squibb’s Opdivo (nivolumab) for the Adjuvant Treatment of Adult Patients with Melanoma with Involvement of Lymph Nodes or Metastatic Disease Who Have Under
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Bristol-Myers Squibb Reports Second Quarter Financial Results
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Bristol-Myers Squibb and Tsinghua University Announce Collaboration to Accelerate Early Research into Potential Therapies for Autoimmune Diseases and Cancer
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Bristol-Myers Squibb Announces Departure of Chief Commercial Officer
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Bristol-Myers Squibb (BMY) Reports Clinical Research Collaboration with Gritstone Oncology to Evaluate Novel Immunotherapy Approach in Advanced Solid Tumors
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Bristol-Myers Squibb and Gritstone Oncology Announce Clinical Research Collaboration to Evaluate Novel Immunotherapy Approach in Advanced Solid Tumors
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Bristol-Myers Squibb (BMY) Opdivo + Low-Dose Yervoy is First Immuno-Oncology Combination Approved for Some MSI-H/dMMR mCRC Patients
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Bristol-Myers Squibb’s Opdivo® (nivolumab) + Low-Dose Yervoy® (ipilimumab) is the First Immuno-Oncology Combination Approved for MSI-H/dMMR mCRC Patients Who Progressed Following Treatment with a
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Bristol-Myers Squibb (BMY) Says EC Approved Expanded Indication for Sprycel
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European Commission Approves Expanded Indication for Sprycel (dasatinib) to Include Treatment of Children with Philadelphia Chromosome-Positive Chronic Myeloid Leukemia in Chronic Phase
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Bristol-Myers Squibb (BMY) Announces Positive CHMP Opinion Recommending Approval of Opdivo for Adjuvant Treatment of Adult Patients with Melanoma
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Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Approval of Opdivo (nivolumab) for the Adjuvant Treatment of Adult Patients with Melanoma
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Bristol-Myers Squibb (BMY) Reports FDA Acceptance of Supplemental Biologics License Application for Opdivo (nivolumab) Plus Low-Dose Yervoy (ipilimumab)
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U.S. Food and Drug Administration (FDA) Accepts Application for Opdivo Plus Low-Dose Yervoy for Treatment of First-Line Non-Small Cell Lung Cancer in Patients with Tumor Mutational Burden ≥10 mut/Mb
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Dallas Cowboys Quarterback Dak Prescott, Modern Family Star Eric Stonestreet and Actress Tia Mowry Call on Americans to Rise Up Against Cancer Through Ready. Raise. Rise.

