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Amgen (AMGN) Completes Acquisition Of Otezla, Updates Guidance
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Amgen Completes Acquisition Of Otezla® (apremilast)
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Bristol-Myers Squibb (BMY) Completes Acquisition of Celgene (CELG)
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Bristol-Myers Squibb Completes Acquisition of Celgene, Creating a Leading Biopharma Company
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Bristol-Myers Squibb (BMY) Announces Update on CheckMate -915 for Opdivo Plus Yervoy (ipilimumab) Versus Opdivo Alone in Patients with Resected High-Risk Melanoma and PD-L1 <1%
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Bristol-Myers Squibb Announces Update on CheckMate -915 for Opdivo (nivolumab) Plus Yervoy (ipilimumab) Versus Opdivo Alone in Patients with Resected High-Risk Melanoma and PD-L1 <1%
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Bristol-Myers (BMY) Receives FTC Clearance for Celgene (CELG) Acquisition, Deal Expected to Close Next Week
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Bristol-Myers Squibb Receives Clearance from U.S. Federal Trade Commission for Celgene Acquisition
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Bristol-Myers Squibb (BMY) Announces FAA Accepts for Priority Review Application for Opdivo Plus Yervoy Combination for Patients with Previously Treated Advanced HCC
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U.S. Food and Drug Administration Accepts for Priority Review Bristol-Myers Squibb’s Application for Opdivo (nivolumab) Plus Yervoy (ipilimumab) Combination for Patients with Previously Treated Adva
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Bristol-Myers Squibb Underscores Precision-Focused Immunology Leadership with New Data on ORENCIA® (abatacept) in Early RA, ACPA-Positive Patients Presented at 2019 ACR/ARP Annual Meeting¹
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Bristol-Myers Squibb Reports Third Quarter Financial Results
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Bristol-Myers Squibb to Take Part at the Wolfe Research Healthcare Conference
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Bristol-Myers Squibb Awards “Golden Tickets” for LabCentral to Carmine Therapeutics, STIMIT
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Bristol-Myers Squibb (BMY) Announces EC Approves Opdivo 4-Week Dosing Schedule for Adjuvant Treatment of Adult Patients with Melanoma with Involvement of Lymph Nodes or Metastatic Disease
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European Commission Approves Opdivo (nivolumab) Four-Week Dosing Schedule for the Adjuvant Treatment of Adult Patients with Melanoma with Involvement of Lymph Nodes or Metastatic Disease Who Have Unde
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Bristol-Myers Squibb (BMY) CheckMate -9LA Meets Primary Endpoint Demonstrating Superior OS Compared to Chemotherapy Alone in First-Line Lung Cancer
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CheckMate -9LA, a Phase 3 Trial Evaluating Opdivo (nivolumab) Plus Low-Dose Yervoy (ipilimumab) Combined with Chemotherapy, Meets Primary Endpoint Demonstrating Superior Overall Survival Compared to C
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Opdivo (nivolumab) Demonstrates Statistically Significant Overall Survival Benefit Versus Chemotherapy in Patients with Advanced Esophageal Cancer
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Bristol-Myers Squibb Announces Final Results from CheckMate -227 Part 1 Demonstrating Superior Overall Survival for Opdivo (nivolumab) Plus Low-Dose Yervoy (ipilimumab) vs. Chemotherapy in Advanced No
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Five-Year Outcomes for Opdivo (nivolumab) in Combination with Yervoy (ipilimumab) Demonstrate Durable Long-Term Survival Benefits in Patients with Advanced Melanoma
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Adjuvant Treatment with Opdivo (nivolumab) Continues to Demonstrate Extended Recurrence-Free Survival at Three Years in Resected High-Risk Melanoma Patients
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Bristol-Myers Squibb (BMY) Reports Positive CHMP Recommendation Approval of Opdivo (nivolumab) Flat Dosing Schedule
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Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Approval of Opdivo (nivolumab) Four-Week Dosing Schedule for the Adjuvant Treatment of Adult Patients with Melanoma with Involvement of
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Bristol-Myers Squibb to Hold Investor Webcast to Discuss ESMO Highlights
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Bristol-Myers Squibb (BMY) Says Research at ESMO Demonstrates Breadth of Oncology Development Program and Focus on Improving OS Across Multiple Cancers
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Bristol-Myers Squibb Research at ESMO Demonstrates Breadth of Oncology Development Program and Focus on Improving Overall Survival Across Multiple Cancers
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Bristol-Myers Squibb to Announce Results for Third Quarter 2019 on October 31, 2019
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Bristol‑Myers Squibb Announces Dividend
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Bristol-Myers Squibb (BMY) Announces Pooled Five-Year Survival Results for Opdivo in Previously-Treated Advanced NSCLC
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Bristol-Myers Squibb Announces Pooled Five-Year Survival Results for Opdivo (nivolumab) in Previously-Treated Advanced Non-Small Cell Lung Cancer Patients
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Bristol-Myers Squibb (BMY) Reports Update on Phase 3 Opdivo (nivolumab) CheckMate -548 Trial
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Bristol-Myers Squibb Provides Update on Phase 3 Opdivo (nivolumab) CheckMate -548 Trial in Patients with Newly Diagnosed MGMT-Methylated Glioblastoma Multiforme
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Press Release Biocartis NV: Biocartis announces H1 2019 results
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BioMotiv and Bristol-Myers Squibb Form Strategic Partnership
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More Than 100 Bristol-Myers Squibb Employees Embark on Coast 2 Coast 4 Cancer Ride to Help Advance Groundbreaking Cancer Research
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Bristol-Myers Squibb to Take Part at the Morgan Stanley Conference
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European Commission Approves Empliciti (elotuzumab) Plus Pomalidomide and Low-Dose Dexamethasone (EPd) for the Treatment of Patients with Relapsed and Refractory Multiple Myeloma
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Amgen (AMGN) to Acquire Otezla from Celgene (CELG) for $13.4B
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Bristol-Myers Squibb Announces Agreement Between Celgene and Amgen to Divest OTEZLA® for $13.4 Billion
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Amgen To Acquire Otezla® For $13.4 Billion In Cash, Or Approximately $11.2 Billion Net Of Anticipated Future Cash Tax Benefits
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PTC Therapeutics Expands Presence in New Jersey by Securing State-of-the-Art Biologics Facility
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Nektar (NKTR) and Bristol-Myers Squibb (BMY) Announce FDA Breakthrough Therapy Designation for Bempegaldesleukin with Opdivo for Treatment of Patients with Untreated Advanced Melanoma
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Nektar Therapeutics and Bristol-Myers Squibb Announce U.S. FDA Breakthrough Therapy Designation for Bempegaldesleukin (NKTR-214) in Combination with Opdivo® (nivolumab) for the Treatment of Patients
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Bristol-Myers Squibb (BMY) Announces European Commission Approval of Pending Acquisition of Celgene (CELG)
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Bristol-Myers Squibb Announces European Commission Approval of Pending Acquisition of Celgene
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Bristol-Myers Squibb (BMY) Receives Positive CHMP Opinion Recommending Approval of Empliciti Plus Pomalidomide and Low-Dose Dexamethasone for Treatment of Patients with R/R MM
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Bristol-Myers Squibb Receives Positive CHMP Opinion Recommending Approval of Empliciti (elotuzumab) Plus Pomalidomide and Low-Dose Dexamethasone for Treatment of Patients with Relapsed and Refractory
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Bristol-Myers Squibb Reports Second Quarter Financial Results
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Bristol-Myers Squibb (BMY) Part 2 of the Phase 3 CheckMate -227 Did Not Meet Primary Endpoint

