BRISTOL MYERS SQUIBB
- Country
- 🇺🇸United States
- Ownership
- -
- Established
- 1989-01-01
- Employees
- 30K
- Market Cap
- $97.5B
- Website
- https://www.bms.com/
Clinical Trials
1.7k
Trial Phases
6 Phases
Drug Approvals
11
Drug Approvals
Clinical Trials
Distribution across different clinical trial phases (1332 trials with phase data)• Click on a phase to view related trials
A Study Comparing BMS-986504 in Combination With Nab-paclitaxel and Gemcitabine Versus Placebo in Combination With Nab-paclitaxel and Gemcitabine in Participants With Untreated Metastatic Pancreatic Ductal Adenocarcinoma With Homozygous MTAP Deletion (MountainTAP-30)
- Conditions
- Pancreatic Ductal Adenocarcinoma
- Interventions
- First Posted Date
- 2025-07-21
- Last Posted Date
- 2025-07-21
- Lead Sponsor
- Bristol-Myers Squibb
- Target Recruit Count
- 470
- Registration Number
- NCT07076121
- Locations
- 🇺🇸
Local Institution - 0142, Phoenix, Arizona, United States
🇺🇸Local Institution - 0306, Springdale, Arkansas, United States
🇺🇸Local Institution - 0157, San Francisco, California, United States
A Study to Evaluate Treatment Patterns, Outcomes, and Healthcare Resource Utilization in Patients With Lower-Risk Myelodysplastic Syndromes Treated With Luspatercept
- First Posted Date
- 2025-07-20
- Last Posted Date
- 2025-07-20
- Lead Sponsor
- Bristol-Myers Squibb
- Target Recruit Count
- 250
- Registration Number
- NCT07075406
- Locations
- 🇺🇸
RTI Health Solutions, Research Triangle Park, North Carolina, United States
Treatment Patterns and Outcomes in Patients With Lower-risk Myelodysplastic Syndromes Treated With Luspatercept in China
- First Posted Date
- 2025-07-18
- Last Posted Date
- 2025-07-18
- Lead Sponsor
- Bristol-Myers Squibb
- Target Recruit Count
- 80
- Registration Number
- NCT07073690
- Locations
- 🇨🇳
Zhijian Xiao, Tianjin, China
A Study to Evaluate Novel KarX and KarT Prototypes Versus the KarXT and KarX-EC Reference Following Single Doses, and to Explore the Effect of Food After Multiple Doses of Selected Prototypes in Healthy Adult Participants
- Conditions
- Healthy Volunteers
- Interventions
- First Posted Date
- 2025-07-14
- Last Posted Date
- 2025-07-14
- Lead Sponsor
- Bristol-Myers Squibb
- Target Recruit Count
- 48
- Registration Number
- NCT07063342
- Locations
- 🇬🇧
Quotient Sciences, Nottingham, Nottinghamshire, United Kingdom
A Study to Compare the Combination of BMS-986504 With Pembrolizumab and Chemotherapy Versus Placebo Plus Pembrolizumab and Chemotherapy in First-line Metastatic Non-small Cell Lung Cancer Participants With Homozygous MTAP Deletion
- Conditions
- Metastatic Non-small Cell Lung Cancer With MTAP Deletion
- Interventions
- First Posted Date
- 2025-07-14
- Last Posted Date
- 2025-07-14
- Lead Sponsor
- Bristol-Myers Squibb
- Target Recruit Count
- 590
- Registration Number
- NCT07063745
- Locations
- 🇺🇸
Local Institution - 0119, Anchorage, Alaska, United States
🇺🇸Local Institution - 0120, Tucson, Arizona, United States
🇺🇸Local Institution - 0135, Springdale, Arkansas, United States
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News
Bristol Myers Squibb's Reblozyl Fails Primary Endpoint in Phase III Myelofibrosis Trial Despite Secondary Benefits
Bristol Myers Squibb's anemia drug Reblozyl failed to meet its primary endpoint of red blood cell transfusion independence in the Phase III INDEPENDENCE trial for myelofibrosis patients.
FDA Advisory Panel Rejects GSK's Blenrep Combination Therapies for Multiple Myeloma
FDA advisers voted 5-3 against approving GSK's Blenrep in combination with bortezomib and dexamethasone for relapsed or refractory multiple myeloma patients.
Bristol Myers Squibb and Pfizer Launch Direct-to-Patient Eliquis Program with 40% Price Discount
Bristol Myers Squibb and Pfizer announced a new direct-to-patient purchasing option for Eliquis (apixaban) through their Eliquis 360 Support program, offering eligible patients a cash price more than 40% below the current $606 list price.
FDA Raises Eye Safety Concerns for GSK's Blenrep Ahead of Advisory Committee Review
The FDA has identified significant ocular toxicity concerns with GSK's Blenrep (belantamab mafodotin) ahead of a July 17 advisory committee meeting to review the drug's reintroduction to the U.S. market.
Insurance Disparities Widen Cancer Survival Gaps Despite Immune Checkpoint Inhibitor Advances
A new American Cancer Society study reveals that immune checkpoint inhibitors, while improving survival across all insurance groups, have widened survival disparities between uninsured patients and those with private insurance for advanced melanoma, lung, and kidney cancers.
AbbVie Acquires In Vivo CAR-T Developer Capstan Therapeutics for Up to $2.1 Billion
AbbVie has agreed to acquire cell therapy developer Capstan Therapeutics in a deal worth up to $2.1 billion in cash, gaining access to innovative in vivo CAR-T technology.
FDA Removes Regulatory Barriers for Bristol Myers Squibb's CAR T-Cell Therapies, Expanding Patient Access
The FDA eliminated Risk Evaluation and Mitigation Strategy (REMS) programs and reduced post-treatment monitoring from four weeks to two weeks for Bristol Myers Squibb's CAR T-cell therapies Breyanzi and Abecma.
FDA Approves Streamlined Access for Bristol Myers Squibb CAR T Cell Therapies
The FDA has approved label updates for Bristol Myers Squibb's CAR T cell therapies Breyanzi and Abecma, reducing patient monitoring requirements and removing Risk Evaluation and Mitigation Strategy (REMS) programs.
Incyte Names Bill Meury as New CEO, Replacing 11-Year Veteran Hervé Hoppenot
Incyte has appointed Bill Meury as its new CEO, effective immediately, replacing Hervé Hoppenot who led the cancer and blood disease drugmaker for 11 years.
Cigna Sues Bristol Myers Squibb Over Alleged Monopoly Practices for Cancer Drug Pomalyst
Cigna filed a federal lawsuit against Bristol Myers Squibb, alleging the company used anti-competitive strategies to maintain a monopoly on Pomalyst, a multiple myeloma treatment that generated $2.7 billion in U.S. sales last year.