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Alvotech Files Annual Report with the SEC

Key Takeaway: Alvotech has submitted its Annual Report for 2025 to the SEC, highlighting its commitment to transparency and regulatory compliance. The report includes details about its financial performance and ongoing projects. The company continues to focus on the development of biosimilars, with five already approved and a pipeline of nine candidates targeting various medical conditions.
Price reaction · baseline $3.11 (2026-03-27 close) · clean, no other ALVO news in the window
day 0 close
+5.8%
day 1
+10.3%
day 3 · peak
+17.4%

Market Sentiment Analysis

POSITIVE FACTORS

  • Alvotech has filed its Annual Report for 2025, indicating transparency.
  • The company has five approved biosimilars, showcasing its market presence.
  • Alvotech is focused on developing a robust pipeline of nine biosimilar candidates.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+128%
120-day peak, hindsight
Typical move
13.8%
average across 7 past catalysts
Lead asset
Stelara
Phase 3 · Psoriasis

Full Press Release Details

REYKJAVIK, Iceland, March 30, 2026 (GLOBE NEWSWIRE) -- Alvotech (NASDAQ: ALVO) (the “Company”) has filed its Annual Report 2025 on Form 20-F for the financial year 2025 with the U.S. Securities and Exchange Commission (SEC), incorporating by reference parts of the Alvotech Annual Report 2025. The report is available on the SEC’s website,www.sec.gov, as well as in the investor relations section of Alvotech’s website athttps://investors.alvotech.com/financials.

MediaBenedikt StefanssonSarah MacLeodalvotech.media@alvotech.com

InvestorsDr. Balaji V Prasad (US)Patrik Ling (SE)Benedikt Stefansson (IS)alvotech.ir@alvotech.com

About AlvotechAlvotech is a biotechnology company, founded by Robert Wessman, focused solely on the development and manufacture of biosimilar medicines for patients worldwide. Alvotech seeks to be a global leader in biosimilars by delivering high-quality, cost-effective products and services, enabled by a fully integrated approach and broad in-house capabilities. Five biosimilars are already approved and marketed in multiple global markets, including biosimilars to Humira®(adalimumab), Stelara®(ustekinumab), Simponi®(golimumab), Eylea®(aflibercept) and Prolia®/Xgeva®(denosumab). The current development pipeline includes nine disclosed biosimilar candidates aimed at treating autoimmune disorders, eye disorders, osteoporosis, respiratory disease, and cancer. Alvotech has formed a network of strategic commercial partnerships to provide global reach and leverage local expertise in markets that include the United States, Europe, Japan, China, and other Asian countries and large parts of South America, Africa and the Middle East. For more information, please visithttps://www.alvotech.com. None of the information on the Alvotech website shall be deemed part of this press release.
For more information, please visit ourinvestor portal, and ourwebsiteor follow us on social media onLinkedIn,Facebook,InstagramandYouTube.

Frequently Asked Questions

What is the purpose of Alvotech's Annual Report?

The Annual Report provides transparency about Alvotech's financial performance and operations.

How many biosimilars does Alvotech have approved?

Alvotech has five approved biosimilars currently marketed in various global markets.

What is included in Alvotech's development pipeline?

The pipeline includes nine disclosed biosimilar candidates targeting multiple medical conditions.

Where can I find Alvotech's Annual Report?

The report is available on the SEC's website and Alvotech's investor relations page.

Last updated: Mar 30, 2026