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GMAB

Genmab A/SNASDAQHealthcare
$27.50+1.03%OpenMarket Cap: $16.98B

As of 2026-04-06

Valuation

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P/E (TTM)

6.15

PEG

P/B

2.85

P/S

0.90

EV/EBITDA

3.80

DCF Value

$6.01

FCF Yield

17.4%

Div Yield

0.0%

Margins & Returns

Gross Margin

94.0%

Operating Margin

36.7%

Net Margin

21.0%

ROE

19.0%

ROA

114.7%

ROIC

50.3%

Financials

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PeriodRevenueNet IncomeEPS
Q4 2025$1.05B$30.9M$0.05
FY 2025$3.72B$963.8M$1.54
Q3 2025$1.02B$401.0M$0.65
Q2 2025$5.86B$2.13B$3.42

Analyst Ratings

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GuggenheimBuy
2026-02-23
HC Wainwright & Co.Buy
2026-02-18
HC Wainwright & Co.Buy
2025-11-10
Truist SecuritiesBuy
2025-11-07
HC Wainwright & Co.Buy
2025-10-02

Company Info

Sector

Healthcare

Industry

Country

DK

Exchange

NASDAQ

Beta

0.74

Genmab A/S develops antibody therapeutics for the treatment of cancer and other diseases primarily in Denmark. The company markets DARZALEX, a human monoclonal antibody for the treatment of patients with multiple myeloma (MM); teprotumumab for the treatment of thyroid eye disease; ofatumurnab, a human monoclonal antibody to treat chronic lymphocytic leukemia (CLL) and multiple sclerosis; and Amivantamab for advanced or metastatic gastric or esophageal cancer and NSCLC. Its products include daratumumab to treat MM, non-MM blood cancers, and AL amyloidosis; GEN1047; tisotumab vedotin for treating cervical, ovarian, and solid cancers; DuoBody-PD-L1x4-1BB, and DuoBody-CD40x4-1BB for treating solid tumors; Epcoritamab for relapsed/refractory diffuse large B-cell lymphoma and chronic lymphocytic leukemia; and HexaBody-CD38 and DuoHexaBody-CD37 for treating hematological malignancies. The company's also develops products, which is in Phase 2 comprise Teclistamab for vaso-occlusive crises; Camidanlumab tesirine to treat hodgkin lymphoma and solid tumors; JNJ-64007957 and JNJ-64407564 to treat MM; PRV-015 for treating celiac disease; Mim8 for treating haemophilia A; and Lu AF82422 for treating multiple system atrophy disease. In addition, it has approximately 20 active pre-clinical programs. The company has a commercial license and collaboration agreement with Seagen Inc. to co-develop tisotumab vedotin. It also has a collaboration agreement with CureVac AG for the research and development of differentiated mRNA-based antibody products; AbbVie for the development of epcoritamab; and collaborations with BioNTech, Janssen, Novo Nordisk A/S, BliNK Biomedical SAS, and Bolt Biotherapeutics, Inc. Genmab A/S was founded in 1999 and is headquartered in Copenhagen, Denmark.

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