Princeton, NJ, United States · Est. 1989 · 34,000 employees
Global biopharmaceutical company focused on innovative medicines for serious diseases.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 3 drugs with upcoming expirations
Pipeline
By Phase
66 drugs in development
By Therapeutic Area
top 6
R&D Momentum
96/100
Pipeline Velocity
77/100
Trial Completion Rate
83/100
Pipeline Concentration
22/100
Pipeline Freshness
68/100
Strategic Signals
Activity
Last 14 days
A Study of Adjunctive Aripiprazole in Patients With Major Depressive Disorder
A Phase 2A, Double-blind, Randomized, Placebo-controlled, Multi-center Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986435/MYK-224 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)
A Phase 3, Two-Stage, Randomized, Multicenter, Open-Label Study Comparing Mezigdomide (CC-92480), Bortezomib and Dexamethasone (MEZIVd) Versus Pomalidomide, Bortezomib and Dexamethasone (PVd) in Subjects With Relapsed or Refractory Multiple Myeloma (RRMM): SUCCESSOR-1
A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer's Disease
A Phase 1, Open-label, Positron Emission Tomography (PET) Imaging Study to Evaluate M4 Muscarinic Acetylcholine Receptor Occupancy in the Central Nervous System Using [11C]MK-6884 PET Tracer Before and After Oral Administration of Multiple Doses of BMS-986521 in Healthy Adult Participants
A Phase 2a Study to Evaluate the Safety and Pharmacokinetics of Luspatercept (ACE-536) in Pediatric Participants With Beta (β)-Thalassemia
A Phase 1 First-in-human Study of BMS-986500 as Monotherapy in Advanced Solid Tumors and as Combination Therapy in CDK4/6 Inhibitor Pre-treated Advanced Breast Cancer
Long-Term Follow-up Protocol for Subjects Treated With Gene-Modified T Cells
Phase 1, 3-Part, Open-label Study to Evaluate the Pharmacokinetics of Novel KarX (BMS-986519) and KarT (BMS-986520) Prototypes Versus the KarXT (BMS-986510) and KarX-EC (BMS-986519) Reference Following Single Doses, and to Explore the Effect of Food After Multiple Doses of Selected Prototypes in Healthy Adult Participants
An Exploratory Phase 1/2 Trial to Determine Recommended Phase 2 Dose (RP2D), Safety and Preliminary Efficacy of bb2121 (Ide-cel) Combinations in Subjects With Relapsed/Refractory Multiple Myeloma (KarMMa-7)
A Phase 3b/4 Multi-center, Randomized, Open-label, Long-term Safety Study of Deucravacitinib in Comparison to Ustekinumab in Participants With Moderate-to-Severe Plaque Psoriasis
IZABRIGHT-Bladder01: A Randomized, Open-label, Phase 2/3 Trial of Izalontamab Brengitecan Versus Platinum-based Chemotherapy for Metastatic Urothelial Cancer in Participants With Disease Progression on or After an Immunotherapy-based Treatment
Details
Company Overview
$115.0B
Mkt Cap
$45.0B
Revenue
$10.3B
Cash
Therapeutic Focus
Recent SEC Filings
BRISTOL MYERS SQUIBB CO (BMY, BMYMP, CELG-RI) (CIK 0000014272)
Pipeline
Regulatory
Stadol — STADOL
Application NDA019890 (NDA)
Videx — VIDEX
Application NDA020156 (NDA)
Videx — VIDEX
Application NDA020154 (NDA)
Serzone — SERZONE
Application NDA020152 (NDA)
Pronestyl — PROCANBID
Application NDA020545 (NDA)
Thalomid — THALOMID
Application NDA020785 (NDA)
BuSpar — BUSPAR
Application NDA021190 (NDA)
Videx — VIDEX EC
Application NDA021183 (NDA)
Orencia — ORENCIA
Application BLA125118 (BLA)
Nulojix — NULOJIX
Application BLA125288 (BLA)
Yervoy — YERVOY
Application BLA125377 (BLA)
Opdivo — OPDIVO
Application BLA125554 (BLA)
Opdivo — Opdivo
Application 125554 (BLA)
Empliciti — EMPLICITI
Application BLA761035 (BLA)
Daklinza — DAKLINZA
Application NDA206843 (NDA)
Reblozyl — REBLOZYL
Application BLA761136 (BLA)
Inrebic — INREBIC
Application NDA212327 (NDA)
OPDUALAG — OPDUALAG
Application BLA761234 (BLA)
Eliquis — ELIQUIS
Application NDA202155 (NDA)
Eliquis — ELIQUIS SPRINKLE
Application NDA220073 (NDA)
BRISTOL MYERS SQUIBB CO (BMY, BMYMP, CELG-RI) (CIK 0000014272)
Accession: 001-01136
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)