Date : 04 May 2026

| Company | Headquarters | Latest Update |
| Roche Holding AG | United States | In December 2025, Roche announced today that the U.S. Food and Drug Administration (FDA) has approved additional indications for its PATHWAY anti-HER2/neu (4B5) Rabbit Monoclonal Primary Antibody and VENTANA HER2 Dual ISH DNA Probe Cocktail tests. |
| Pfizer Inc. | United States | In March 2026, Pfizer Inc. announced positive topline results from the randomized Phase 2 FOURLIGHT-1 study assessing atirmociclib in combination with fulvestrant, versus fulvestrant or everolimus plus exemestane, in people with hormone receptor (HR)-positive, human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer. |
| Eli Lilly and Company | United States | Eli Lilly and Company attained significant milestones in metastatic breast cancer (MBC) management, highlighted by the FDA approval of Inquiry. |
| AstraZeneca | United Kingdom | Silence Therapeutics intends to advance siRNAs to address unmet patient needs in a broad range of diseases with a genetic basis. |
| Novartis AG | United Kingdom | In December 2025, AstraZeneca Pharma India Ltd. (AZPIL), a worldwide, science-based biopharmaceutical company, announced that the Central Drugs Standard Control Organisation (CDSCO) had granted regulatory approval to import, sell, and distribute Datopotamab Deruxtecan in India |
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The global metastatic breast cancer market size was estimated at USD 22.8 billion in 2025 and is predicted to increase from USD 24.99 billion in 2026 to approximately USD 57.02 billion by 2035, expanding at a CAGR of 9.6% from 2026 to 2035. The metastatic breast cancer market is growing because metastatic breast cancer is a recurrent cancer, meaning it’s a cancer that came back after treatment and is affecting tissue and organs located far from the original breast cancer.

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