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BRISTOL MYERS SQUIBB

🇺🇸United States
Ownership
-
Established
1989-01-01
Employees
30K
Market Cap
$97.5B
Website
https://www.bms.com/

Clinical Trials

1.7k

Active:129
Completed:1196

Trial Phases

6 Phases

Early Phase 1:1
Phase 1:574
Phase 2:352
+3 more phases

Drug Approvals

11

SFDA:10
CIMA_AEMPS:1

Drug Approvals

REVIA COMPRIMIDOS RECUBIERTOS

Approval Date
Jul 14, 2025
CIMA_AEMPS

Clinical Trials

Distribution across different clinical trial phases (1332 trials with phase data)• Click on a phase to view related trials

Phase 1
574 (43.1%)
Phase 2
352 (26.4%)
Phase 3
320 (24.0%)
Phase 4
53 (4.0%)
Not Applicable
29 (2.2%)
phase_1_2
2 (0.2%)
Early Phase 1
1 (0.1%)
phase_2_3
1 (0.1%)

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)

Not Applicable
Not yet recruiting
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

and more 248 locations

A Study to Evaluate Treatment Patterns, Outcomes, and Healthcare Resource Utilization in Patients With Lower-Risk Myelodysplastic Syndromes Treated With Luspatercept

Active, not recruiting
Conditions
Myelodysplastic Syndromes
Interventions
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

Active, not recruiting
Conditions
Myelodysplastic Syndromes
Interventions
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

Not Applicable
Recruiting
Conditions
Healthy Volunteers
Interventions
Drug: Xanomeline/Trospium Chloride Capsule
Drug: Xanomeline Enteric Capsule
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

Not Applicable
Not yet recruiting
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

and more 164 locations
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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.

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