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

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.

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

As of October 30, 2025

48
 

Compounds in development

40+
 

Disease areas being studied

In the Pipeline

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

Development Partnerships:  Anti-CCR8 + nivolumab, nivolumab + relatlimab HD, OPDIVO, YERVOY: Ono; AUGTYRO, COBENFY (KarXT): Zai Lab; BMS-986495: Prothena; pumitamig (BNT327/BMS-986545): BioNTech; iza-bren: SystImmune; milvexian: Johnson & Johnson; obexelimab: Zenas BioPharma; REBLOZYL: Merck; rHuPH20: Halozyme

Reference notes:

 *    Partner-run study
(NME) New Molecular Entity Lead Indication 


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.