In the pipeline

Our pipeline is focused on research in therapeutic areas where we can accelerate the development of transformational, life-changing medicines for patients

Our pipeline at a glance

As of February 06, 2025

50

Compounds in development

40+

Disease areas being studied

Like any other scientific endeavor, clinical testing of novel drug compounds is a complex, time-consuming, resource-intensive process with no guaranteed results. But, as described here, Bristol Myers Squibb is committed to pursuing such clinical development and, in doing so, to bringing new hope to patients.

In the pipeline

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The safety and efficacy of investigational agents and/or investigational uses of approved products have not been established. 

Brand Name / Compound
Research Area / Line of Therapy
Phase 1 P 1
Phase 2 P 2
Phase 3 P 3

Please click on product name to see the Full U.S. Prescribing Information for KRAZATI®, OPDIVO®, OPDUALAG, REBLOZYL®, BREYANZI®, SOTYKTU, and COBENFY including Boxed WARNINGS for BREYANZI®.

Development Partnership: Anti-CCR8 + nivolumab, nivolumab + relatlimab HD, OPDIVO, OPDUALAG, YERVOY: Ono; AUGTYRO, COBENFY, KRAZATI: Zai Lab; BMS-986495: Prothena; iza-bren (EGFRxHER3 ADC): SystImmune; milvexian: Johnson & Johnson; obexelimab: Zenas BioPharma; PKCθ Inhibitor: Exscientia; REBLOZYL: Merck; rHuPH20: Halozyme

* Partner-run study
✦ NME Lead Indication
     NSCLC = Non-Small Cell Lung Cancer
     SCLC = Small Cell Lung Cancer
     ADC = Antibody Drug Conjugate


For information on approved uses, refer to approved product labeling. Phase I - clinical trials investigating safety of an investigational medicine in a small number of human subjects. Phase II - clinical trials investigating dosing, safety and efficacy of an investigational medicine in a small number of patients who have the disease or condition under study. Phase III - clinical trials investigating the safety and efficacy of an investigational medicine in a larger number of patients who have the disease or condition under study. For purposes of this chart, this includes the regulatory approval process prior to receiving marketing approval in the first major market.