Analysts have increased their price target for Eisai from ¥4,857.69 to ¥4,988.46. They cite slightly improved profit margin forecasts despite marginally lower expectations for revenue growth.
What's in the News
- Eisai and Biogen launched the LEQEMBI IQLIK subcutaneous injection in the U.S. for maintenance dosing in Alzheimer’s disease patients. This offers an at-home treatment alternative after initial intravenous therapy (Key Developments).
- The LEQEMBI Companion program and app were introduced to provide injection training, educational resources, and support for patients and caregivers throughout their treatment journey (Key Developments).
- Lecanemab (Leqembi) received approval in China and Australia for maintenance intravenous dosing, expanding its global regulatory footprint for early Alzheimer’s disease (Key Developments).
- Eisai entered a settlement agreement allowing Dr. Reddy’s Laboratories to launch a generic version of Lenvima in the U.S. from July 2030. Patent litigation with Torrent Pharmaceuticals remains ongoing (Key Developments).
- The U.S. FDA granted Fast Track designation to Eisai’s investigational anti-tau antibody etalanetug (E2814) for Alzheimer’s disease, supporting expedited development of novel treatments (Key Developments).
Valuation Changes
- Consensus Analyst Price Target has risen slightly from ¥4,857.69 to ¥4,988.46.
- Discount Rate remains essentially unchanged at 4.72%.
- Revenue Growth expectations have fallen modestly from 3.93% to 3.78%.
- Net Profit Margin is forecast to improve slightly, increasing from 7.46% to 7.53%.
- Future P/E ratio has increased marginally from 23.32x to 23.83x.
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