MAAT INDEX

CLAIM #12257 · Bristol-Myers Squibb Company (BMY) · 2026Q1 earnings call · Apr 30, 2026 · due Dec 31, 2030

We anticipate these readouts will help us further diversify and broaden our portfolio and are part of our efforts to deliver more than 10 new medicines and 30 meaningful life cycle management opportunities by the end of the decade.

Chris Boerner · CEO

PENDING
graded after results covering Dec 31, 2030 are reported

How to check this claim

Look at: Cumulative count of new medicine approvals and life cycle management indication/label expansions delivered by the company since goal announcement

It came true if: New medicines approved >= 10 AND life cycle management opportunities delivered >= 30, by end of decade

Where: Company-disclosed pipeline/portfolio milestones (investor presentations, 10-K, press releases on approvals and label expansions)

In context

Hodgkin lymphoma indications. We also reported positive Phase I switch data for cobi positive Phase III data for KEMZYOS in adolescents with obstructive HCM and positive Phase II data for Reblozyl in alpha thalassemia. Stepping back, these updates reflect the diversity and breadth of our pipeline, both in terms of therapeutic areas and modalities as well as continued execution across the business. Moving to Slide 5. As we've said, the latter part of 2026 is shaping up to include an increasing cadence of pivotal readouts that are expected to further define and derisk our long-term growth profile. Among the Phase III readouts expected late in the year, our Milvexian and atrial fibrillation and secondary stroke prevention, Cobenfy Alzheimer's psychosis at [indiscernible] iberdomide PFS data. We anticipate these readouts will help us further diversify and broaden our portfolio and are part of our efforts to deliver more than 10 new medicines and 30 meaningful life cycle management opportunities by the end of the decade. Turning to Slide 6. We Central to delivering on these opportunities and enabling sustained long-term growth are our efforts to drive top-tier R&D productivity. In our development organization, we continue to improve execution across drug development by upgrading talent, streamlining decision-making and instituting tighter management of core clinical activities. We are also focused on enhancing the quality and depth of our early to mid-stage pipeline. Underpinning these efforts are investments we are making in core R&D infrastructure, including broadening the use of AI tools together with laboratory automation and people trained in the right ways of working. In research and early development, target selection and molecule design can have an outsized impact on long-term value. We have set a

Verify independently

SEC filings for BMY · Claim quote is verbatim from the 2026Q1 earnings call.