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Genmab A/S

GMAB· NASDAQ
DKDK
$54.92-3.75%
2026-11-02

Financials

Valuation Metrics

Genmab A/S's Market Cap is $33.72B. At end of 2025 it was $18.98B. Ranked #411 of 3,118 in US market (top 13%), #120 of 1,474 on NASDAQ (top 8%), #25 of 265 in Pharmaceuticals, Biotechnology & Life Sciences (top 9%) by Market Cap.

Investment Metrics(as of 2026-11-02)

MetricValue
Size
Market Cap$33.72B
Net Income$788M
Total Assets$12.52B
Net Assets$5.96B
Employees3,119
Value
P/E42.78x
P/B5.66x
P/S9.06x
EV/EBITDA30.74x
FCF Yield2.57%
Profitability
ROE13.23%
ROA6.30%
Financial Health
Debt Ratio110.09%
Total Debt$5.27B
FCF$867M
Cash$1.50B
Current Ratio2.46x
Net Debt/EBITDA3.09x
Performance
1Y Return91.96%
1M Return58.04%
From 52W High-8.42%
1Y MDD-32.51%
Trading
Volume3,941,458 shares
Trading Value$219M
Per Share
EPS$1.28
BPS$9.70

Company Info

CEO Jan van de Winkel
Employees 3,119
HQ Copenhagen, DK

Genmab A/S, a biopharmaceutical company founded in 1999 and headquartered in Copenhagen, Denmark, specializes in the discovery and development of innovative antibody therapies primarily for treating cancer and various other serious illnesses. The company's commercialized portfolio includes several key products: DARZALEX (daratumumab), a human monoclonal antibody for multiple myeloma (MM), non-MM blood cancers, and AL amyloidosis; teprotumumab, indicated for thyroid eye disease; ofatumumab, another human monoclonal antibody used in chronic lymphocytic leukemia (CLL) and multiple sclerosis; Amivantamab, for advanced or metastatic gastric or esophageal cancer and non-small cell lung cancer (NSCLC); and tisotumab vedotin, which targets cervical, ovarian, and solid tumors. Genmab maintains a robust pipeline of investigational medicines. These include GEN1047; DuoBody-PD-L1x4-1BB and DuoBody-CD40x4-1BB, both developed for solid tumors; Epcoritamab, in development for relapsed/refractory diffuse large B-cell lymphoma and chronic lymphocytic leukemia; and HexaBody-CD38 and DuoHexaBody-CD37, aimed at hematological malignancies. Furthermore, the company has several products in Phase 2 clinical trials: Teclistamab for vaso-occlusive crises; Camidanlumab tesirine for Hodgkin lymphoma and solid tumors; JNJ-64007957 and JNJ-64407564 for MM; PRV-015 for celiac disease; Mim8 for haemophilia A; and Lu AF82422 for multiple system atrophy disease. In addition to its clinical programs, Genmab is advancing approximately 20 active pre-clinical programs. Genmab fosters strategic collaborations to further its research and development efforts. It holds a commercial license and co-development agreement with Seagen Inc. for tisotumab vedotin. The company also partners with CureVac AG on the research and development of differentiated mRNA-based antibody products and with AbbVie for the development of epcoritamab. Further alliances include BioNTech, Janssen, Novo Nordisk A/S, BliNK Biomedical SAS, and Bolt Biotherapeutics, Inc.