Press Releases March 30, 2026 07:55 PM

Alvotech Publishes 2025 Annual Report

Alvotech releases 2025 Annual Report highlighting biosimilar advancements and strategic partnerships

By Ajmal Hussain
Share
Twitter Reddit Facebook LinkedIn
ALVO

Alvotech, a Nasdaq-listed biotechnology firm specializing in biosimilars, has published its 2025 Annual Report. The company continues its focus on developing and commercializing high-quality biosimilar medicines globally, with five biosimilars already approved and marketed. Their pipeline includes nine biosimilar candidates targeting multiple therapeutic areas, and they maintain extensive strategic partnerships across major global markets.

Alvotech Publishes 2025 Annual Report
ALVO
Summarize with
ChatGPT Perplexity Claude Grok Gemini

Key Points

  • Alvotech published its 2025 Annual Report detailing financials and operations.
  • The company has five approved and marketed biosimilars targeting autoimmune, eye, bone, respiratory diseases, and cancer.
  • Alvotech has a robust development pipeline and strategic partnerships for global market reach including the US, Europe, and Asia.

REYKJAVIK, ICELAND (March 30, 2026) — Alvotech (NASDAQ: ALVO) (the “Company”) has published its Annual Report for 2025. The report is available in the investor relations section of Alvotech’s website at: https://investors.alvotech.com/financials and is attached to this announcement in PDF and iXBRL formats.

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.

Attachments

  • Alvotech Consolidated Financial Statements FY 2025
  • 222100DCZBOWV5DZ8372-2025-12-31-1-en

Risks

  • Competitive biotech and pharmaceutical industry dynamics could impact market share and revenue growth.
  • Regulatory approvals for biosimilars remain a risk affecting pipeline commercialization timelines.
  • Dependence on partnerships to penetrate global markets introduces geopolitical and operational uncertainties.

More from Press Releases

Agios Showcases RISE UP Phase 3 Results at EHA 2026 Plenary Session Reinforcing Strong Anti-Hemolytic Profile of Mitapivat in Sickle Cell Disease Jun 13, 2026 Rhythm Pharmaceuticals Presents Positive Interim Six-month Data from Phase 2 Trial of Setmelanotide in Patients with Prader-Willi Syndrome (PWS) at ENDO 2026 Jun 13, 2026 Intellia Therapeutics Reports Additional Positive Phase 3 Results for Lonvoguran Ziclumeran (lonvo-z) in Patients with Hereditary Angioedema Jun 13, 2026 Arcadia Biosciences (RKDA) Announces Closing of $4 Million Private Placement Priced At-The-Market Under Nasdaq Rules Jun 12, 2026 Belite Bio Completes Rolling Submission of New Drug Application to U.S. Food and Drug Administration for Tinlarebant for the Treatment of Stargardt Disease Type 1 Jun 12, 2026