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CLAIM #48659 · Pfizer Inc (PFE) · 2025Q4 earnings call · Feb 3, 2026 · due Dec 31, 2026

If successful, we will substantially expand the US addressable population with approximately 22,500 additional patients across both cis-eligible and cis-ineligible muscle-invasive bladder cancer, up from about 19,000 patients in metastatic urothelial cancer.

Albert Bourla · CEO

PENDING
graded after results covering Dec 31, 2026 are reported

How to check this claim

Look at: FDA regulatory decision/approval status for PADCEV in cisplatin-eligible muscle-invasive bladder cancer (MIBC)

It came true if: FDA approval granted for cis-eligible MIBC indication (approval occurs = success; no approval or rejection = miss)

Where: FDA approval announcements, company press releases, Pfizer 10-K/10-Q pipeline disclosures

In context

y exclusivity in the next few years. Albert Bourla: Seagen, Metaira, and Biohaven are the most significant strategic acquisitions in recent years. They have transformative potential for Pfizer Inc., and we are focused on maximizing the value of in-line product portfolios and accelerating pipeline development. We made continued progress last year integrating legacy Seagen products into our commercial portfolio. I'm also pleased with notable advances in our development programs, including recent FDA approval for PATCEV in combination with pembrolizumab for patients with muscle-invasive bladder cancer who are ineligible for cisplatin-containing chemotherapies. We are encouraged by the opportunity to build on this with an expected regulatory decision for patients with cisplatin-eligible MIBC. If successful, we will substantially expand the US addressable population with approximately 22,500 additional patients across both cis-eligible and cis-ineligible muscle-invasive bladder cancer, up from about 19,000 patients in metastatic urothelial cancer. We have a clear strategy aiming for Pfizer Inc. leadership in the next generation of therapies for chronic weight management with a highly differentiated Metsera pipeline portfolio, our Yaopharm exclusive global collaboration and licensing agreement, and other Pfizer Inc. programs such as our oral GPR antagonist candidate. Since closing our Biohaven acquisition a few years ago, we have globally scaled a leading migraine portfolio. It strengthened our product mix to drive significant impact both for patients and our commercial performance. Nurtec has a strong market leadership position in the oral CGRP class in 2025. In Q4, we captured 83% of new CGRP writer volume and remain the leader in new patient starts. I expect 2026 to be also a very rich year for key catalysts and to intend to deli

Verify independently

SEC filings for PFE · Claim quote is verbatim from the 2025Q4 earnings call.