Genmab Reports 2025 Net Sales of DARZALEX® Totaling USD 14,351 Million
Copenhagen, Denmark; January 21, 2026 – Genmab A/S (Nasdaq: GMAB) today announced its worldwide net trade sales for DARZALEX® (daratumumab) reached an impressive USD 14,351 million in 2025. This figure includes net sales from the subcutaneous (SC) formulation, marketed as DARZALEX FASPRO® in the U.S., as reported by Johnson & Johnson (J&J) subsidiary Janssen Biotech, Inc.
Sales Breakdown and Genmab's Royalties
The net sales of DARZALEX were broken down into:
- USD 8,266 million in the United States
- USD 6,085 million from the rest of the world
Genmab benefits from these sales through royalties under its exclusive worldwide license with J&J, which encompasses both the intravenous and SC forms of daratumumab.
About Genmab: A Leader in Antibody Therapies
Established in 1999, Genmab is a global biotechnology company focused on developing innovative antibody medicines aimed at improving the lives of patients with cancer and other serious diseases. With over 25 years of expertise, Genmab has advanced various antibody-based therapeutic formats, including:
- Bispecific antibodies
- Antibody-drug conjugates (ADCs)
- Immune-modulating antibodies
- Next-generation modalities
Currently, Genmab's science underpins eight approved antibody therapies, and the company boasts a robust late-stage clinical pipeline with several wholly owned programs focused on delivering transformative medicines to patients.
Global Presence and Investor Relations
Headquartered in Copenhagen, Denmark, Genmab maintains a strong international presence, including operations in North America, Europe, and the Asia Pacific region. For inquiries and further information, interested parties can reach out to:
- Marisol Peron, Senior Vice President, Global Communications & Corporate Affairs
- Phone: +1 609 524 0065
- Email: mmp@genmab.com
- Andrew Carlsen, Vice President, Head of Investor Relations
- Phone: +45 3377 9558
- Email: acn@genmab.com
Forward-Looking Statements and Disclaimer
This announcement includes forward-looking statements. Genmab cautions that actual results may differ materially due to various risks, including uncertainties related to clinical development and market acceptance. For more details, please refer to Genmab’s latest financial reports and the Annual Report on Form 20-F available through the U.S. Securities and Exchange Commission.