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Bristol-Myers Squibb
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FDA Approval
U.S. Food and Drug Administration Approves Bristol Myers Squibb’s Zeposia® (ozanimod), an Oral Treatment for Adults with Moderately to Severely Active Ulcerative Colitis
Bristol-Myers Squibb
PR-M06-21-008
Jun 07, 2021
Collaboration
Dragonfly Therapeutics and Bristol Myers Squibb Announce Exclusive Global License for Dragonfly’s IL-12 Investigational Immunotherapy Program
Bristol-Myers Squibb
PR-M08-20-NI-35
Aug 20, 2020
Diversity
Bristol Myers Squibb and the Bristol Myers Squibb Foundation Commit $300 Million to Accelerate and Expand Health Equity and Diversity and Inclusion Efforts
Bristol-Myers Squibb
PR-M08-20-NI-20
Aug 13, 2020
FDA
FDA Accepts for Priority Review Bristol Myers Squibb’s Application for CC-486 for Maintenance Treatment of Adult Patients in Remission with Acute Myeloid Leukemia
Bristol-Myers Squibb
PR-M05-20-NI-012
May 08, 2020
Healthcare
Bristol Myers Squibb Expands Patient Support Programs to Help Newly Uninsured Patients in the U.S.
Bristol-Myers Squibb
PR-M04-20-NI-010
Apr 07, 2020
Digital Therapeutics
Voluntis and Bristol-Myers Squibb to Co-Develop Digital Therapeutics for Oncology
Bristol-Myers Squibb
PR-M03-20-NI-011
Mar 06, 2020
Collaboration
Evotec and Bristol-Myers Squibb Expand iPSC Collaboration
Evotec
PR-M01-20-NI-018
Jan 14, 2020
Bristol-Myers Squibb Announces Update for Patients with Resected High-Risk Melanoma and PD-L1 <1%
Bristol-Myers Squibb
PA1904
Nov 29, 2019
Collaboration
Presage Announces Collaboration with Bristol-Myers Squibb for Phase O Studies of Novel Cancer Agents Utilizing CIVO™ Technology
Presage Biosciences
PR-M09-19-NI-002
Sep 03, 2019
M&A
Bristol-Myers Squibb Provides Update on Pending Merger with Celgene
Bristol-Myers Squibb
PR-M06-19-NI-051
Jun 26, 2019
M&A
BMS–Celgene Merger Still On
Nice Insight
PAO-M05-19-NI-007
May 02, 2019
M&A
Bristol-Myers Squibb to Acquire Celgene to Create a Premier Innovative Biopharma Company
Bristol-Myers Squibb
PR-M01-19-NI-017
Jan 03, 2019
Oncology
Bristol-Myers Squibb and Infinity Pharmaceuticals Announce a New Clinical Collaboration to Evaluate Opdivo (Nivolumab) in Combination with IPI-549 in Urothelial Cancer
Infinity Pharmaceuticals
PR-M11-18-NI-029
Nov 08, 2018
FDA Approval
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
Bristol-Myers Squibb
PR-M09-18-NI-065
Sep 21, 2018
Funding
IFM Gets Funding to Support Work on NLRP3 Inhibitors
Nigel Walker
Nice Insight
PAO-M07-18-NI-016
Jul 24, 2018
U.S. Food and Drug Administration Accepts Supplemental Biologics License Application for Opdivo (nivolumab)
Bristol-Myers Squibb
PR-M04-18-NI-85
Apr 24, 2018
Cardiovascular
Janssen Announces Worldwide Development and Commercialization Collaboration with Bristol-Myers Squibb to Advance a Next-Generation Therapy for Cardiovascular Diseases
Janssen Pharmaceutical Companies
PR-M04-18-NI-72
Apr 20, 2018
Collaboration
Bristol-Myers Squibb and Illumina Announce Strategic Collaboration to Develop and Commercialize Companion Diagnostics
Bristol-Myers Squibb
PR-M04-18-NI-64
Apr 19, 2018
Oncology
Opdivo (nivolumab), First PD-1 Inhibitor to Demonstrate Superior Survival Benefit Compared with Chemotherapy
Bristol-Myers Squibb
PR-M04-18-NI-65
Apr 19, 2018
Strategic Collaboration
Bristol-Myers Squibb and Nektar Therapeutics Announce Global Development & Commercialization Collaboration for Nektar’s CD122-biased Agonist, NKTR-214
Bristol-Myers Squibb
PR-M02-18-NI-73
Feb 20, 2018