GMAB Genmab A/S
HealthcareAs of 2026-05-25
Valuation
View DetailsP/E (TTM)
6.33
PEG
—
P/B
2.90
P/S
1.15
EV/EBITDA
5.33
DCF Value
$6.06
FCF Yield
7.0%
Div Yield
0.0%
Margins & Returns
Gross Margin
93.9%
Operating Margin
39.6%
Net Margin
18.2%
ROE
20.5%
ROA
21.1%
ROIC
43.8%
Financials
View All| Period | Revenue | Net Income | EPS |
|---|---|---|---|
| Q1 null | $899.3M | $53.2M | $— |
| Q4 null | $1.05B | $30.9M | $— |
| FY null | $3.72B | $963.8M | $— |
| Q3 null | $1.02B | $401.0M | $— |
Analyst Ratings
View AllConsensus
Buy
Target (Consensus)
$37.88
Target (Median)
$39.00
Target Range
$32.00 - $41.50
Company Info
Sector
Healthcare
Industry
Biotechnology
Country
DK
Exchange
—
Beta
0.69
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.