Eisai reports JPY 88 billion FY2025 LEQEMBI revenue, while Biogen’s Q1 2026 data show 74% growth, indicating its rising role in Alzheimer’s disease treatment.
Written By: Samiksha Jadhav, BPharm
Reviewed By: Pharmacally Editorial Team
Eisai Co., Ltd. reported that its anti-amyloid-beta protofibril antibody LEQEMBI® (lecanemab) generated JPY 88.0 billion in global revenue for fiscal year 2025 (April 2025–March 2026), marking the therapy’s first full year of meaningful commercial contribution in Alzheimer’s disease. The United States accounted for the largest share at JPY 44.6 billion, followed by Japan at JPY 24.4 billion and China at JPY 12.4 billion, reflecting stronger early adoption in markets with more established diagnostic pathways and reimbursement systems.
Complementing this annual performance, Biogen Inc.’s first quarter 2026 results show continued commercial momentum. The company reported global in-market sales of $168 million for LEQEMBI, representing a 74% year-over-year increase, including $86 million from the United States, indicating sustained sequential growth and expanding physician uptake. Biogen’s Alzheimer’s collaboration revenue reached $59.5 million, up 80% year-over-year, highlighting the growing financial contribution from the LEQEMBI collaboration.
Region/Metric | Eisai FY2025 (JPY Bn / ~USD M) | Biogen Q1 2026 (USD M) |
United States | 44.6 / ~303 | 86 |
Japan | 24.4 / ~166 | Included in ROW |
China | 12.4 / ~84 | Included in ROW |
Rest-of-World (ROW) | Balance | 82 |
Total | 88.0 / ~598 | 168 |
Taken together, Eisai’s full-year revenue and Biogen’s quarterly performance indicate that LEQEMBI has moved beyond the initial launch phase into a scaling commercial phase. The United States remains the primary growth driver, supported by improving access and clinical adoption, while Japan provides a stable contribution and China continues to develop as an emerging market.
Real-world data further support the therapy’s uptake, with Biogen reporting that approximately 78% of patients remained on LEQEMBI at 18 months, with many continuing into the maintenance phase. This level of persistence suggests sustained treatment continuity, which is important for long-term revenue visibility in a chronic neurodegenerative disease setting.
Eisai leads global development and regulatory activities for lecanemab, while both Eisai and Biogen co-commercialize and co-promote the therapy, combining development leadership with commercial execution across key markets.
Overall, strong annual revenue, continued quarterly growth, and early real-world persistence data position LEQEMBI as a core revenue driver in Alzheimer’s disease therapeutics, while future uptake will remain influenced by factors such as diagnostic capacity, treatment infrastructure, and long-term access across global markets.
Reference
Revenue of LEQEMBI® (Preliminary Basis), April 29, 2026, No.26-24
Biogen reports strong first quarter 2026 results, April 29, 2026, Exhibit 99.1 – Q1 2026 Press Release
About the Writer
Samiksha Vikram Jadhav is a B. Pharm graduate with a strong academic foundation in pharmaceutical sciences, pharmacology, and drug development. She specializes in pharma market research, with a focused interest in mergers and acquisitions, strategic partnerships, and global pharma and biotech deals. Her work centers on analyzing industry transactions, market positioning, and business strategies, translating complex developments into clear, accurate, and insightful scientific and commercial reporting.
