
Last 4 earnings calls · through Q2 FY2026
The bull case is that newer medicines are already large enough that their combined growth covers most of what generics take from the older portfolio each year.
It rests on approvals coming from the company's own pipeline in myeloma, pulmonary fibrosis and anticoagulation, which would add revenue independent of Eliquis.
Management has cut operating costs while raising guidance, so the company meets the Eliquis patent expiry with a lower expense base and more cash than a year ago.
The company has beaten its own guidance repeatedly, which supports the claim that its commercial organization can launch new drugs quickly once they are approved.
The bear case is that revenue depends heavily on Eliquis, whose U.S. patent expires soon, so the company must replace a large base while still building one.
It points to pivotal trial dates moving later and to a schizophrenia launch that is growing slowly, which pushes the pipeline payoff further into the future.
It argues that negotiated prices and large discounts already lowered what Eliquis earns, so cash generated before expiry is smaller than the sales line implies.
In short: Newer drugs are growing faster than generics erode the legacy portfolio, while key readouts have slipped.
An approval in August would make it the first CELMoD on the market and let BMS replace Revlimid and Pomalyst in second-line myeloma with an oral drug it owns.
In February management projected a 12% to 16% legacy decline this year; it now expects 4% to 6% and has raised full-year revenue and adjusted earnings guidance.
Milvexian's atrial fibrillation data slipped from late 2026 to the first quarter of 2027, and Alzheimer's psychosis data for Cobenfy now begin in early 2027.
A year ago management expected continued steady growth; it now says it must accelerate new patient starts and repeat prescribing, which points to slower-than-planned adoption.
Opdivo revenue fell 2.9% to $2.5 billion as the subcutaneous version takes share of the same franchise, so conversion adds convenience but no net new sales.
In short: Cost cuts hold the operating margin steady while gross margin falls on a shift toward Eliquis sales.
Operating margin was 31.0%, slightly above a year earlier, as savings from the productivity program offset spending behind new launches and the pumitamig program.
Net debt fell to $32.1 billion from $35.6 billion a year earlier, cutting interest costs and leaving more cash for business development and the dividend.
Gross margin fell to 71.3% and management guides 2026 to 69% to 70%, because more Eliquis and less Revlimid and Pomalyst revenue carry lower profit per dollar.
Free cash flow over the last twelve months was $11.4 billion against $14.6 billion a year earlier, partly because the Eliquis list price cut reduced collections.
In short: Eliquis dominates U.S. anticoagulation, but its patent expires in 2028 and the government now sets its price.
A roughly 40% list price cut combined with the Medicare negotiated price removed accumulated inflation rebates, helping Eliquis revenue rise 21.8% to $4.5 billion.
If approved it would face no other oral Factor XI drug in atrial fibrillation, and BMS can sell it through the Eliquis sales force as that brand loses exclusivity.
It is a first-in-class LPA1 drug with phase two data showing better lung function and placebo-like tolerability, in a market management thinks could double in size.
Eliquis is 35% of segment revenue and its European patent expires late in 2026, after which generic entry typically produces steep and rapid sales declines.
Eliquis and Pomalyst have both gone through government price negotiation, and management is still in talks with the administration on most-favored-nation pricing and tariffs.