Atirmociclib (CDK4 Inhibitor)
PfizerPFE
- Indication
- HR-Positive, HER2-Negative Advanced Or Metastatic Breast Cancer
- Stage
- Phase 2
- Event
- Phase 2 Data readout
- Details
April 21, 2026 — Pfizer Inc. (NYSE: PFE) announced it will present new oncology data at the American Society of Clinical Oncology (ASCO) Annual Meeting (May 29–June 2, 2026, Chicago), spanning more than 40 company-, investigator-, and partner-sponsored abstracts, including three late-breaking sessions and eight oral/rapid oral presentations.
Key clinical updates highlighted include: a 7-year update from the Phase 3 CROWN study supporting LORBRENA (lorlatinib) as a guideline-recommended first-line therapy for ALK-positive metastatic NSCLC; late-breaking PFS and OS results from Cohort 3 of the Phase 3 BREAKWATER trial evaluating BRAFTOVI (encorafenib) + cetuximab + FOLFIRI as first-line treatment for BRAF V600E-mutant metastatic colorectal cancer; and late-breaking Phase 3 TALAPRO-3 results showing clinically meaningful rPFS benefit and a strong OS trend for TALZENNA (talazoparib) + XTANDI (enzalutamide) in mCSPC with HRR gene alterations.
Pfizer also cited data supporting earlier-line use of TUKYSA (tucatinib) as first-line maintenance in HER2+ metastatic breast cancer and provided updates on pipeline assets including PF-08634404 (PD-1/VEGF bispecific), sigvotatug vedotin (ADC), and atirmociclib (CDK4 inhibitor), underscoring potential new standards of care and pipeline breadth.
- Source
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Financial Snapshot
Market Cap
$149.2B
Price
$25.63