Eisai Co., Ltd.
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About the company
Eisai Co. , Ltd. , a pharmaceutical company headquartered in Tokyo, Japan, develops and markets a wide array of medicinal products.
- CEO
- Haruo Naito
- IPO
- 2011
- Employees
- 10,543
- HQ
- Tokyo, TY, JP
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Similar companies
Peers in the same neighborhood.
- Market Cap
- $8.44B
- P/E
- 33.06
- Fwd P/E
- 0.15
- PEG
- -2.10
- P/S
- 1.63
- P/B
- 1.54
- EV/EBITDA
- 14.02
- Div Yield
- 3.22%
- Gross Margin
- 76.70%
- Op Margin
- 5.11%
- Net Margin
- 4.94%
- ROE
- 4.77%
- ROIC
- 2.88%
Latest fiscal year · YoY change
- Revenue
- $830.57B+5.2%
- Gross Profit
- $638.15B+2.8%
- Op Income
- $40.46B
- Net Income
- $38.80B-16.4%
- EPS
- $137.41-16.1%
- OCF Growth
- +104.9%
- FCF Growth
- +547.1%
- 52W High
- $35.83
- 52W Low
- $23.88
- 50D MA
- $26.34
- 200D MA
- $28.71
- Beta
- -0.05
- RSI (14)
- 72
- Avg Volume
- 67
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
Eisai delivered a strong Q1 with double-digit revenue and profit growth, driven by LENVIMA, DAYVIGO and LEQEMBI, while management highlighted early progress toward full-year targets and a key U.S. launch for LEQEMBI IQLIK.· August 3, 2026
- Q1 revenue rose 15.6% year over year to JPY 234.3 billion; operating profit increased 19.2% to JPY 24.7 billion, and profit for the period rose 26% to JPY 18.2 billion.
- Gross profit was JPY 183.2 billion, up 14.5%, while cost of sales was JPY 51.1 billion and the cost ratio was 21.8%.
- Major products drove growth: LENVIMA revenue was JPY 97.3 billion (+16%), DAYVIGO JPY 18.9 billion (+38%), and LEQEMBI JPY 29.3 billion (+27%).
- Management said progress toward the full-year forecast is on track, with revenue at 26.5%-27% and operating profit at 35.3% of plan.
- LEQEMBI IQLIK won U.S. initiation-treatment approval on July 13, with sales expected to begin in late August; management framed it as a major step for access and long-term growth.
Eisai reported Q1 fiscal 2026 revenue of JPY 234.3 billion, up 15.6% year over year, operating profit of JPY 24.7 billion, up 19.2%, gross profit of JPY 183.2 billion, up 14.5%, and profit for the period of JPY 18.2 billion, up 26%. Cost of sales was JPY 51.1 billion and the cost of sales ratio was 21.8%; R&D expenses were JPY 43.7 billion, up 12.7%, and SG&A was JPY 114.8 billion, up 14.6%. Management said the company is steadily progressing toward its FY2026 forecast, with revenue at 26.5%-27% of plan and operating profit/core operating profit at 35.3% of plan. No new full-year numerical guidance was changed on the call; management reiterated FY targets for LENVIMA (JPY 345 billion), DAYVIGO (JPY 73.5 billion), and LEQEMBI (JPY 143.5 billion).
COO Haruo Naito said the company’s growth is being driven by the three core products, with LEQEMBI, DAYVIGO and LENVIMA all expanding and supporting both revenue and profit. He emphasized that Eisai is not just selling products but building the access infrastructure needed for LEQEMBI, including reimbursement, diagnosis flow, specialty pharmacy coordination and home administration support. His tone was confident and strategic, with repeated focus on maximizing LEQEMBI’s value, expanding the orexin platform, and building the next wave of AD therapies around amyloid, tau and neurodegeneration.
CFO Takuya Oyama highlighted that Q1 results were stronger than the plan, even after excluding foreign exchange benefits, and said the quarter was a “good start” toward the full-year forecast. He pointed to lower product-level cost ratios for LEQEMBI and DAYVIGO, and said LENVIMA’s strong revenue, including FX support, also helped the margin profile. He noted that forex added JPY 18.9 billion to revenue year over year and a JPY 1.38 billion positive impact to operating profit, but said the operating profit impact was limited because both revenue and many costs are foreign-currency denominated.
Analysts focused on why gross profit and cost of sales were better than expected, the impact of foreign exchange, and whether LEQEMBI IQLIK could contribute quickly and profitably. Management said product-level cost ratios improved, revenue beat the plan even after FX, and the company is investing in LEQEMBI SG&A ahead of further revenue growth in Q2-Q4. On reimbursement, management said it expects IQLIK initiation therapy to follow a scheme similar to maintenance therapy, with eventual formulary inclusion, and on pricing it said IQLIK is designed for parity with IV on a total medical cost basis while reflecting convenience and lower non-drug costs.
The call showed broad momentum across the portfolio, with all three growth products posting strong year-over-year gains and management saying the company is ahead of plan. LEQEMBI IQLIK approval creates a new access and convenience lever, and management believes it can expand patient starts, improve retention, and strengthen competitive positioning. Eisai also pointed to promising pipeline catalysts in AD and orexin, suggesting multiple longer-term growth drivers beyond the current portfolio.
Management also signaled that commercialization of IQLIK still depends on reimbursement, access workflows, specialty pharmacy coordination, and home-administration support, so approval alone does not guarantee rapid uptake. LEQEMBI growth is still tied to building diagnosis and treatment infrastructure, and the company is continuing to spend on SG&A and R&D ahead of future expansion. In the pipeline, several key programs still need clinical readouts, including ledasorexton Phase II data and later-stage AD studies in fiscal 2027 and fiscal 2028, so longer-term value remains dependent on execution and trial results.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 90.1%
- Shares Outstanding
- 282.24M
- Float Shares
- 254.22M
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Generate ESALF report →Eisai Co., Ltd. (ESAIY) Q1 2027 Earnings Call Transcript
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prnewswire.com · Apr 9
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