BMS Streamlines Pipeline, Dropping Two Clinical Programs Amid Leadership Changes

Bristol Myers Squibb (BMS) has announced the removal of two clinical programs from its pipeline, signaling a strategic shift in the company's research and development focus. This decision comes alongside recent leadership transitions and ongoing cost-saving initiatives at the pharmaceutical giant.
Pipeline Adjustments and Program Discontinuations
BMS has cut ties with two clinical-stage assets, as revealed in their third-quarter earnings presentation on October 30. The first program, an SOS1 inhibitor coded as MRTX0902, originated from the company's 2023 acquisition of Mirati Therapeutics. This asset was under investigation in a phase 1/2 solid tumor trial, which began in 2022 and was expected to yield primary results by mid-2026.
The second discontinued program is EXS4318, a PKC-theta inhibitor developed in partnership with Exscientia (now known as Recursion). This immunology and inflammation asset, which entered human trials in 2023, was part of a $1.2 billion biobucks discovery deal signed in 2021.
Strategic Implications and Ongoing Developments
Despite these cuts, BMS continues to advance other programs acquired through recent deals. The company is proceeding with the development of MRTX1719, another Mirati program currently in phase 1 testing for solid tumors with MTAP deletion.
The pipeline adjustments coincide with BMS's leadership transition, as former Chief Medical Officer Samit Hirawat, M.D., has been succeeded by AstraZeneca's Cristian Massacesi, M.D. During a recent call, Massacesi emphasized the company's focus on neuroscience, particularly highlighting ongoing work related to the approved schizophrenia treatment Cobenfy. He noted that 14 studies, including 10 pivotal trials, are either in progress or being initiated for this drug.
Financial Considerations and Future Outlook
These strategic moves align with BMS's broader cost-saving initiative, which aims to achieve $1.5 billion in savings by the end of the year. The company's decision to streamline its pipeline reflects a careful evaluation of its research portfolio and resource allocation in a competitive pharmaceutical landscape.
As BMS continues to refine its pipeline and research strategy, industry observers will be watching closely to see how these changes impact the company's long-term growth and innovation potential in key therapeutic areas.
References
- BMS removes 2 clinical programs from pipeline, one from Mirati and another from Exscientia
Bristol Myers Squibb is shedding two clinical programs from its in-house pipeline, one from its 2023 Mirati buyout and another from a partnership with U.K. biotech Exscientia, now known as Recursion.
Explore Further
What were the specific scientific or financial reasons behind the decision to discontinue the MRTX0902 and EXS4318 programs?
How does the development of MRTX1719 for solid tumors with MTAP deletion align with BMS’s broader research priorities?
What are Bristol Myers Squibb’s strategies for advancing neuroscience research, especially around the schizophrenia treatment Cobenfy?
How might the $1.5 billion cost-saving initiative impact the company's ability to innovate in drug development?
What are the potential implications of Cristian Massacesi’s leadership transition for BMS’s pipeline strategy and future collaborations?