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Also trades as: GMAB.CO (CPH) · $vol 55M · GNMSF (OTC) · $vol 1M · GE9.F (FSX) · $vol 0M

GMAB NASDAQ

Genmab A/S
1W: +16.1% 1M: +26.5% 3M: +54.1% YTD: +40.5% 1Y: +49.6% 3Y: +56.0% 5Y: +0.4%
$44.67
-0.01 (-0.03%)
After Hours: $44.30 (-0.37, -0.83%)
Weekly Expected Move ±8.1%
$37 $40 $44 $47 $51
NASDAQ · Healthcare · Biotechnology · Tech Score Strong Buy · Power 70 · $27.5B mcap · 587M float · 0.486% daily turnover · Short 61% of daily vol
Credit Risk of going bust: lower than 69% of companies Debt: 16.1% of company value Bonds: $301.5M held by 241 funds, 181 bp over Treasuries → details ▾
If the stock fell to about $0.65 (down 99%), Genmab A/S would be worth roughly what it owes.
Total debt $5.27B against a stock market value of $27.48B.
Distance to default 7.47 (Merton model): prices to 2026-10-26, balance sheet 2026-06-30, debt counted $2.71B (short-term plus half of long-term), stock volatility 35.1%; Altman Z'' 3.61. A ranking and a back-test, not a forecast.
Bond figures are fund-reported marks (SEC N-PORT) as of Jul 2026. How these are computed.
Smart Money Score
Moderate 50
Insider—
Congress—
ETF Holdings—
Key Statistics
Market Cap$27.5B
52W Range23.62-45.445
Volume7,437,414
Avg Volume2,851,800
Beta0.65
Dividend—
Analyst Ratings
14 Buy 3 Hold 1 Sell
Consensus Buy
Company Info
CEOJan van de Winkel
Employees3,119
SectorHealthcare
IndustryBiotechnology
IPO Date2009-06-01
Websitegenmab.com
Carl Jacobsens Vej 30
Copenhagen, CD 2500
DK
45 70 20 27 28
About Genmab A/S

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.

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For informational purposes only. Not investment advice. Data sourced from SEC filings. Privacy Terms