Bristol Myers Squibb reported Q4 2025 revenue of $12.5 billion, representing a 1% increase year-over-year. Non-GAAP EPS for the quarter was $1.26, a 25% decrease compared to the prior year, primarily due to a $(0.60) per share impact from acquired in-process R&D (IPRD) charges and licensing income. For the full year 2025, revenue totaled $48.2 billion, which was relatively flat compared to 2024. The Growth Portfolio, led by Reblozyl (+22%), Camzyos (+59%), and Breyanzi (+49%), surged 17% in 2025 to $26.4 billion, now accounting for 55% of total company revenue. This expansion helped offset a 15% decline in the Legacy Portfolio, where Revlimid sales plummeted following the expiration of volume limits in January 2026.
Note: Bristol Myers Squibb's FY'25 ended on December 31, 2025.
In March 2026, Bristol Myers Squibb announced that its Phase 3 trial for mezigdomide, a targeted protein degrader (CELMoD), met its primary endpoint of progression-free survival in patients with relapsed or refractory multiple myeloma. This follows similar success for iberdomide, which is currently under FDA review with a decision date set for August 2026. These next-generation oral therapies are strategically critical for BMY as they are designed to replace the revenue streams of aging blockbusters Revlimid and Pomalyst. Management expects these CELMoDs, alongside the GPRC5D-targeted CAR T zola-cel (BMS-986393), to define the company's long-term dominance in hematology through 2030.
Below are key drivers of Bristol Myers Squibb's value that present opportunities for upside or downside to the current Trefis price estimate:
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Bristol Myers Squibb is a global biopharmaceutical leader focused on oncology, hematology, immunology, and cardiovascular disease. The company's business model is currently in a high-stakes transition phase, as it aggressively reinvests cash flows from its legacy blockbuster Eliquis into a diversified "Growth Portfolio" of over 10 high-margin assets. This strategy relies on rapid clinical execution in immunology and targeted protein degradation to mitigate a projected $10 billion revenue gap caused by patent expirations throughout the late 2020s.
The Oncology and Hematology segment remains the primary value driver, contributing the majority of the company's operating profit through established franchises and high-growth cell therapies.
The combination of Opdivo and Yervoy maintains a massive installed base in first-line lung cancer and melanoma. Despite looming patent cliffs for Opdivo in 2028, the franchise remains a cash cow, with Q4 2025 combined revenue exceeding $3.5 billion.
BMY holds a significant competitive advantage in the multiple myeloma space with its end-to-end portfolio. The rapid scaling of Breyanzi and the upcoming commercialization of the CELMoD platform (iberdomide and mezigdomide) create a high-moat ecosystem that is difficult for competitors to displace.
Eliquis continues to be the world's leading oral anticoagulant, growing 8% in Q4 2025 to $3.5 billion. Its massive market share provides BMY with a unique scale advantage in cardiovascular care as it develops milvexian to secure the next decade of market leadership.
The industry is shifting from traditional protein inhibition to protein degradation (CELMoDs). BMY is positioned as the leader in this space, leveraging technology acquired from Celgene to develop oral "tagging" therapies that can overcome resistance where previous drugs failed.
BMY is implementing a $2.0 billion productivity initiative intended to streamline operations by the end of 2027. The strategy involves scaling AI across R&D and commercial functions to lower OpEx and accelerate the "time-to-market" for the 2026-2027 clinical wave.
Management has prioritized strengthening the balance sheet following a period of intense M&A. Having paid down $10 billion in debt ahead of schedule by early 2026, BMY is pivoting toward a balanced approach of dividend growth and bolt-on acquisitions to bolster the late-stage pipeline.