Eisai Co., Ltd.
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About the company
Eisai Co. , Ltd. is a Japanese pharmaceutical firm deeply involved in the entire lifecycle of drug development, from initial research and innovation to manufacturing, distribution, and international trade within Japan.
- CEO
- Haruo Naito
- IPO
- 2023
- Employees
- 10,543
- HQ
- Tokyo, TY, JP
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- Market Cap
- $8.69B
- P/E
- 33.06
- Fwd P/E
- 0.20
- 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
- $825.38B+4.6%
- Gross Profit
- $634.15B+2.2%
- Op Income
- $44.14B
- Net Income
- $38.56B-17.0%
- EPS
- $34.20-16.5%
- OCF Growth
- +115.9%
- FCF Growth
- +581.8%
- 52W High
- $9.22
- 52W Low
- $5.69
- 50D MA
- $6.78
- 200D MA
- $7.23
- Beta
- -0.07
- RSI (14)
- 61
- Avg Volume
- 218.43K
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
Eisai posted a strong Q1 fiscal 2026 with double-digit revenue and operating profit growth, led by LENVIMA, DAYVIGO and LEQEMBI, while LEQEMBI IQLIK and BBM are positioned to expand future growth.· August 3, 2026
- Q1 revenue was JPY 234.3 billion, up 15.6% year on year, and operating profit was JPY 24.7 billion, up 19.2%.
- Gross profit rose to JPY 183.2 billion, while R&D was JPY 43.7 billion and SG&A was JPY 114.8 billion.
- LEQEMBI, DAYVIGO and LENVIMA all posted strong growth; management said progress toward the FY2026 forecast is on track.
- LEQEMBI IQLIK was approved in the U.S. for initiation treatment on July 13, with launch expected in late August.
- Management said first-quarter results beat plan even after foreign exchange effects, and the company posted its first-ever quarterly commercial-basis profit excluding LEQEMBI R&D expenses.
Eisai reported first-quarter fiscal 2026 revenue of JPY 234.3 billion, up 15.6% year on year, with operating profit of JPY 24.7 billion, up 19.2%. Gross profit was JPY 183.2 billion, up 14.5%; cost of sales was JPY 51.1 billion with a 21.8% cost ratio; R&D expense was JPY 43.7 billion, up 12.7%; and SG&A was JPY 114.8 billion, up 14.6%. Profit for the period was JPY 18.2 billion, up 26%. By product, LENVIMA revenue was JPY 97.3 billion, up 16%; DAYVIGO revenue was JPY 18.9 billion, up 38%; and LEQEMBI revenue was JPY 29.3 billion, up 27%. Management said revenue progress toward the full-year forecast was 26.5%-27% and operating profit progress was 35.3%. For full-year guidance, management reiterated targets of JPY 345 billion for LENVIMA, JPY 73.5 billion for DAYVIGO, and JPY 143.5 billion for LEQEMBI. They said the company is on track to achieve its FY2026 forecast and expects continued LEQEMBI growth from IQLIK and blood-based biomarker adoption. No next-quarter quantitative guidance was given on the call.
Haruo Naito framed the quarter as evidence that Eisai’s three growth products are building a stronger long-term base. He emphasized that LEQEMBI is moving into a new phase with IQLIK, broader access infrastructure, and real-world evidence supporting continued treatment, while BBM should help widen diagnosis and treatment access. His tone was confident and strategic, focused on turning convenience and diagnostic innovation into durable growth.
Takuya Oyama said the quarter benefited from strong organic growth and better-than-planned results, including a positive foreign exchange impact of JPY 18.9 billion on revenue and a JPY 1.38 billion positive impact on operating profit. He noted cost of sales was JPY 51.1 billion, the cost ratio was 21.8%, and that product-level cost ratios for LEQEMBI and DAYVIGO improved; LENVIMA also had a very low cost ratio, helped by FX and product mix. He added that SG&A rose due to profit-sharing tied to LENVIMA and proactive LEQEMBI investment, and said the company aims to reach commercial-basis profitability excluding LEQEMBI R&D expenses.
Analysts focused on why first-quarter margins and operating profit were stronger than expected, and Oyama said the company exceeded its plan even after adjusting for FX, with lower product-level cost ratios and strong LENVIMA revenue. Questions also centered on LEQEMBI IQLIK reimbursement, pricing, and launch timing; management said they expect similar reimbursement treatment to maintenance therapy, that launch is slated for late August, and that prescriptions have already started even though sales have not yet been recorded. On competition, management said LEQEMBI can convert patients from Kisunla in practice and believes IQLIK plus better access infrastructure will strengthen LEQEMBI’s market share.
The quarter showed broad momentum across Eisai’s core products, with all three growth drivers posting double-digit gains and management saying the business is tracking ahead of plan. LEQEMBI’s U.S. growth, the approved IQLIK option, and expanding BBM testing could make treatment easier to start and sustain, while real-world data and retention metrics were presented as supportive evidence.
Management acknowledged that LEQEMBI growth still depends on building reimbursement, diagnosis, and home-administration infrastructure before the product can fully benefit from IQLIK. They also said some areas remain in prioritized launch mode, and SG&A is still being pushed up by LEQEMBI investment and LENVIMA profit-sharing. On the pipeline side, several important data readouts are still ahead, including ledasorexton in fiscal 2026 and key AD studies in fiscal 2027-2028.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 24.9%
- Shares Outstanding
- 1.13B
- Float Shares
- 281.28M
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Generate ESAIY report →Eisai Co., Ltd. (ESAIY) Q1 2027 Earnings Call Transcript
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Eisai Co., Ltd. (ESAIY) Q4 2026 Earnings Call Transcript
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reuters.com · Apr 21
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marketwatch.com · Apr 18
Eisai to Present the Latest Data on Real-World Treatment with Lecanemab and Supporting a Standardized Framework for Treating Early Alzheimer's Disease at the 78th American Academy of Neurology's Annual Meeting
prnewswire.com · Apr 9
Eisai and Nuvation Bio Announce Marketing Authorisation Application for Taletrectinib for the Treatment of Advanced ROS1-Positive Non-Small Cell Lung Cancer Validated by the European Medicines Agency
prnewswire.com · Mar 26
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