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Eisai projects Leqembi® revenue to total JPY 143.5 billion for fiscal year 2026 (April 2026 - March 2027)

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(High)
Rhea-AI Sentiment
(Positive)
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BioArctic (Nasdaq Stockholm: BIOA B) announced that partner Eisai projects Leqembi sales of JPY 143.5 billion (about SEK 8.4 billion) for FY 2026 (April 2026–March 2027), a 63% increase year over year.

This is expected to generate roughly SEK 880 million in royalties to BioArctic. The companies are preparing joint commercialization of Leqembi for Alzheimer's disease in the Nordic region.

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AI-generated analysis. Not financial advice.

Positive

  • Eisai projects FY 2026 Leqembi sales of JPY 143.5 billion
  • Projected Leqembi sales imply 63% growth versus prior fiscal year
  • BioArctic expects about SEK 880 million in Leqembi royalties FY 2026
  • Planned joint Leqembi commercialization with Eisai in the Nordic region

Negative

  • None.

News Market Reaction – B

-5.91%
1 alert
-5.91% News Effect

On the day this news was published, B declined 5.91%, reflecting a notable negative market reaction.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Projected Leqembi revenue: JPY 143.5 billion Projected Leqembi revenue (SEK): SEK 8.4 billion Revenue growth: 63 percent +4 more
7 metrics
Projected Leqembi revenue JPY 143.5 billion Eisai FY 2026 (April 2026–March 2027)
Projected Leqembi revenue (SEK) SEK 8.4 billion Eisai FY 2026 equivalent
Revenue growth 63 percent Leqembi sales growth vs previous year
Projected royalty to BioArctic SEK 880 M Royalty from Leqembi for FY 2026
Q1 2026 report date May 20, 2026 BioArctic Q1 2026 report publication
Report publication time 08.00 a.m. CET BioArctic Q1 2026 report release time
Disclosure release time 08:30 CET Information released for public disclosure

Market Reality Check

Price: $39.40 Vol: Volume 8,301,800 vs 20-da...
low vol
$39.40 Last Close
Volume Volume 8,301,800 vs 20-day average 13,010,112 (relative volume 0.64x) indicates lighter-than-usual trading. low
Technical Price 43.145 trades above the 200-day MA of 38.56, sitting 21.11% below the 52-week high of 54.69 and 147.82% above the 52-week low of 17.41.

Peers on Argus

The stock fell 3.81%, while peers WPM (-1.72%), FNV (-0.41%), AU (-0.88%), AEM (...

The stock fell 3.81%, while peers WPM (-1.72%), FNV (-0.41%), AU (-0.88%), AEM (-1.73%) and KGC (-0.99%) also declined, indicating a sector-wide downward move despite company-specific positive news.

Historical Context

5 past events · Latest: May 13 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
May 13 Sector valuation update Positive -2.1% Sector-wide reset in gold valuations and record cash flows highlighted.
May 13 Earnings presentation invite Neutral -2.1% Announcement of date and webcast details for Q1 2026 report.
May 12 Spin-off prospectus Neutral -2.5% Prospectus and listing details for Octave Intelligence distribution.
May 11 Quarterly earnings Positive +9.0% Q1 2026 beat on production and earnings with strong cash flow.
May 11 Share repurchase plan Positive +9.0% Board authorization of up to $3.0 billion in share buybacks.
Pattern Detected

Recent news has mostly seen price moves align with the tone of events, except for one positive sector-valuation piece that coincided with a decline.

Recent Company History

Over recent months, the company’s news flow has focused on strong operating performance, corporate actions, and sector positioning. On May 11, 2026, Q1 2026 results and a new $3.0 billion buyback drove a +8.97% reaction, reinforcing a pattern of gains on clearly supportive fundamentals. Other items, including a spin-off prospectus and an investor presentation invitation in mid-May 2026, saw modest declines. A sector-wide valuation article on May 13, 2026 also coincided with a negative move, showing that not all positive narratives have translated into price strength.

Market Pulse Summary

The stock moved -5.9% in the session following this news. A negative reaction despite positive reven...
Analysis

The stock moved -5.9% in the session following this news. A negative reaction despite positive revenue and royalty projections fits past instances where constructive narratives did not always translate into gains. The article points to Leqembi revenue of JPY 143.5 billion and royalties of about SEK 880 M, but broader sector pressure or positioning could have outweighed this. History shows at least one prior positive sector-focused update coinciding with a decline, underscoring that sentiment and macro factors can dominate fundamentals at times.

Key Terms

eu market abuse regulation
1 terms
eu market abuse regulation regulatory
"information that BioArctic AB (publ) is obliged to disclose pursuant to the EU Market Abuse Regulation."
A set of EU-wide rules that prevent cheating in financial markets by banning insider trading, market manipulation, and misleading disclosure; it also requires timely public release of key company information so everyone can play on a level field. For investors, it reduces the risk that prices are driven by secret deals or false signals, making markets fairer and more reliable for deciding when to buy or sell — like referees enforcing fair play in a game.

AI-generated analysis. Not financial advice.

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STOCKHOLM, May 15, 2026 /PRNewswire/ -- BioArctic AB's (publ) (Nasdaq Stockholm: BIOA B) partner Eisai today announced that Leqembi sales are expected to total JPY 143.5 billion (approximately SEK 8.4 billion) for their fiscal year (FY) 2026 (April 2026 through March 2027), corresponding to a 63 percent growth compared to the previous year. This would generate approximately SEK 880 M in royalty to BioArctic during the same period.

Leqembi is the result of a long-standing collaboration between BioArctic and Eisai, and the antibody was originally developed by BioArctic based on the work of Professor Lars Lannfelt and his discovery of the Arctic mutation in Alzheimer's disease. Eisai is responsible for clinical development, marketing authorization applications and commercialization of Leqembi for Alzheimer's disease. BioArctic has the right to commercialize Leqembi in the Nordic region together with Eisai, and the two companies are currently preparing for a joint commercialization in the region.

BioArctic's report for the first quarter 2026 will be published on May 20 at 08.00 a.m. CET.

This information is information that BioArctic AB (publ) is obliged to disclose pursuant to the EU Market Abuse Regulation. The information was released for public disclosure, through the agency of the contact person below, on May 15, 2026, at 08:30 CET.

For further information, please contact: 
Oskar Bosson, VP Communications and Investor Relations
E-mail: oskar.bosson@bioarctic.com
Telephone: +46 704 107 180

Jenny Ljunggren, External Communications and Investor Relations Manager
E-mail: jenny.ljunggren@bioarctic.com
Telephone: +46 76 013 86 08

About Leqembi® (lecanemab)

Leqembi is the result of a strategic research alliance between BioArctic and Eisai. It is a humanized immunoglobulin gamma 1 (IgG1) monoclonal antibody directed against aggregated soluble (protofibril) and insoluble forms of amyloid-beta (Aβ).

Leqembi is approved in 53 countries and is under regulatory review in 6 countries. Following the initial phase with treatment every two weeks for 18 months, intravenous (IV) maintenance dosing with treatment every four weeks is approved in 7 countries, including the United Kingdom, China, the US and Japan, and applications have been filed in 12 countries and regions. In the US, Leqembi Iqlik™ is approved for subcutaneous dosing with an autoinjector for maintenance treatment of early Alzheimer's disease. In November 2025, a new drug application for subcutaneous formulation of Leqembi was submitted in Japan. In December 2025, Leqembi was included in the "Commercial Insurance Innovative Drug List", recently introduced by the National Healthcare Security Administration (NHSA) of China. In January 2026, Eisai's supplemental Biologics License Application regarding a subcutaneous starting dose with Leqembi Iqlik was granted Priority Review by the US FDA. The PDUFA date is set to August 24, 2026. In January 2026, the Biologics License Application for subcutaneous formulation of Leqembi was accepted in China and in February, the application was designated for priority review.

Since July 2020, Eisai's Phase 3 clinical study (AHEAD 3-45) with lecanemab in individuals with preclinical Alzheimer's disease meaning they are clinically normal and have intermediate or elevated levels of amyloid in their brains, is ongoing. The study was fully recruited in October 2024. AHEAD 3-45 is a four-year study conducted as a public-private partnership between Eisai, Biogen and the Alzheimer's Clinical Trial Consortium that provides the infrastructure for academic clinical trials in Alzheimer's disease and related dementias in the US, funded by the National Institute on Aging, part of the National Institutes of Health. Since January 2022, the Tau NexGen clinical study for Dominantly Inherited Alzheimer's disease (DIAD), that is conducted by Dominantly Inherited Alzheimer Network Trials Unit (DIAN-TU), led by Washington University School of Medicine in St. Louis, is ongoing and includes lecanemab as the backbone anti-amyloid therapy.

About the collaboration between BioArctic and Eisai

Since 2005, BioArctic has a long-term collaboration with Eisai regarding the development and commercialization of drugs for the treatment of Alzheimer's disease. The most important agreements are the Development and Commercialization agreement for the lecanemab antibody, which was signed 2007, and the Development and Commercialization agreement for the antibody lecanemab back-up for Alzheimer's disease, which was signed 2015. In 2014, Eisai and Biogen entered into a joint development and commercialization agreement for lecanemab. Eisai is responsible for the clinical development, application for market approval and commercialization of the products for Alzheimer's disease. BioArctic has the right to commercialize lecanemab in the Nordic region and is currently preparing for commercialization in the Nordics together with Eisai. BioArctic has no development costs for lecanemab in Alzheimer's disease and is entitled to payments in connection with sales milestones as well as royalties on global sales.

About BioArctic AB

BioArctic AB (publ) is a Swedish research-based biopharma company focusing on innovative treatments that can delay or stop the progression of neurodegenerative diseases. The company invented Leqembi® (lecanemab) – the world's first drug proven to slow the progression of the disease and reduce cognitive impairment in early Alzheimer's disease. Leqembi has been developed together with BioArctic's partner Eisai, who are responsible for regulatory interactions and commercialization globally. In addition to Leqembi, BioArctic has a broad research portfolio with antibodies against Parkinson's disease and ALS as well as additional projects against Alzheimer's disease. Several of the projects utilize the company's proprietary BrainTransporter™ technology, which has the potential to actively transport antibodies across the blood-brain barrier to enhance the efficacy of the treatment. BioArctic's B share (BIOA B) is listed on Nasdaq Stockholm Large Cap. For further information, please visit www.bioarctic.com.

This information was brought to you by Cision http://news.cision.com.

https://news.cision.com/bioarctic/r/eisai-projects-leqembi--revenue-to-total-jpy-143-5-billion-for-fiscal-year-2026--april-2026---march-,c4348851

The following files are available for download:

https://mb.cision.com/Main/9978/4348851/4093642.pdf

​​​​​​​Eisai projects Leqembi® revenue to total JPY 143.5 billion for fiscal year 2026 (April 2026 â€" March 2027)

 

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SOURCE BioArctic

FAQ

What Leqembi revenue has Eisai projected for FY 2026 and its impact on BioArctic (B)?

Eisai projects Leqembi revenue of JPY 143.5 billion for FY 2026. According to BioArctic, this level of sales would generate approximately SEK 880 million in royalty income for the company during the same period, linked to their Leqembi collaboration.

How much royalty revenue could BioArctic (B) receive from Leqembi in fiscal year 2026?

BioArctic expects around SEK 880 million in royalty revenue from Leqembi in FY 2026. According to BioArctic, this estimate is based on Eisai’s sales projection of JPY 143.5 billion for Leqembi between April 2026 and March 2027.

What growth rate is implied by Eisai’s FY 2026 Leqembi forecast relevant to BioArctic (B)?

Eisai’s FY 2026 Leqembi sales forecast implies 63% year-over-year growth. According to BioArctic, this projected increase compared to the previous fiscal year supports higher expected royalty income from Leqembi for the company over the same period.

What is the relationship between BioArctic (B) and Eisai regarding Leqembi for Alzheimer’s disease?

Leqembi originates from BioArctic’s antibody development and Arctic mutation research, while Eisai leads clinical development and global commercialization. According to BioArctic, the companies share rights, with BioArctic able to commercialize Leqembi in the Nordic region together with Eisai.

How are BioArctic (B) and Eisai planning to commercialize Leqembi in the Nordic region?

BioArctic and Eisai are preparing a joint commercialization of Leqembi in the Nordic region. According to BioArctic, the company holds rights to commercialize Leqembi there together with Eisai, complementing Eisai’s broader responsibilities for development and global marketing.