Press Releases March 30, 2026 07:58 PM

Alvotech files Annual Report with the SEC

Alvotech files 2025 Annual Report with the SEC, detailing biosimilar development and commercial strategy

By Nina Shah
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ALVO

Alvotech, a biotechnology firm specializing in biosimilar medicines, has filed its 2025 Annual Report with the U.S. SEC. The report highlights the company's portfolio of approved biosimilars and an active pipeline targeting multiple therapeutic areas, supported by strategic global partnerships for market expansion.

Alvotech files Annual Report with the SEC
ALVO
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Key Points

  • Alvotech has five approved and marketed biosimilars targeting major biologic drugs like Humira and Stelara.
  • The development pipeline includes nine biosimilar candidates addressing autoimmune, eye, bone, respiratory disorders and cancer.
  • Strategic partnerships enable Alvotech to access global markets, including the U.S., Europe, Japan, China, and emerging markets in Asia, South America, Africa, and the Middle East.

REYKJAVIK, ICELAND (March 30, 2026) — 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 at https://investors.alvotech.com/financials.

For further information, contact:

Media
Benedikt Stefansson
Sarah MacLeod
[email protected]

Investors
Dr. Balaji V Prasad (US)
Patrik Ling (SE)
Benedikt Stefansson (IS)
[email protected]

About Alvotech
Alvotech 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 visit https://www.alvotech.com. None of the information on the Alvotech website shall be deemed part of this press release.

For more information, please visit our investor portal, and our website or follow us on social media on LinkedIn, Facebook, Instagram and YouTube.


Risks

  • Dependence on regulatory approvals and market acceptance for biosimilar products, which can impact revenue projections.
  • Competition in the biosimilar sector from other biotech firms and innovator biologics potentially impacting market share.
  • Challenges in global commercialization, including pricing pressures, reimbursement, and potential patent litigations in different jurisdictions.

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