GMAB

Genmab AS
NASDAQHEALTHCAREBIOTECHNOLOGY

Key Statistics

Market Cap
$22.75B
P/E Ratio
29.13
EPS
$1.27
Beta
0.65
52W High
$40.17
52W Low
$23.62
50-Day MA
$34.17
200-Day MA
$29.83
Dividend Yield
—
Profit Margin
19.10%
Forward P/E
15.08
PEG Ratio
4.36

About Genmab AS

Genmab A / S develops antibody therapies for the treatment of cancer and other diseases mainly in Denmark. The company is headquartered in Copenhagen, Denmark.

Official WebsiteUSAFY End: December

Fundamentals

Revenue (TTM)$4.13B
Gross Profit (TTM)$3.84B
EBITDA$1.38B
Operating Margin35.20%
Return on Equity14.00%
Return on Assets8.79%
Revenue/Share (TTM)$6.71
Book Value$9.98
Price-to-Book3.59
Price-to-Sales (TTM)5.51
EV/Revenue6.14
EV/EBITDA19.98
Quarterly Earnings Growth (YoY)-9.40%
Quarterly Revenue Growth (YoY)24.90%
Shares Outstanding$614.90M
Float$552.96M
% Insiders0.00%
% Institutions20.02%

Historical Volatility

HV 10-Day
62.69%
HV 20-Day
45.99%
HV 30-Day
41.25%
HV 60-Day
35.20%
HV Rank
92.9%

Volatility is currently expanding

Analyst Ratings

Consensus ($44.40 target)
1
Strong Buy
9
Buy
1
Hold

Latest News

Genmab Announces Net Sales of DARZALEX® (daratumumab) for Third Quarter of 2026

Company Announcement Net sales of DARZALEX ® in the third quarter of 2026 totaled USD 4,239 million Genmab receives royalties on worldwide net sales from Johnson & Johnson (J&J, legal entity Janssen Biotech, Inc.) COPENHAGEN, Denmark; October 13, 2026 – Genmab A/S (Nasdaq: GMAB) announced today that worldwide net trade sales of DARZALEX (daratumumab), including sales of the subcutaneous (SC) product ( daratumumab and hyaluronidase-fihj , sold under the tradename DARZALEX FASPRO ® in the U.S. ) , as reported by J&J were USD 4,239 million in the third quarter of 2026. Net trade sales were USD 2,528 million in the U.S. and USD 1,711 million in the rest of the world.

GlobeNewsWire10/13/2026Neutral
Genmab: Epkinly Shines In Phase 3 DLBCL Trial

Genmab delivered strong topline results for Epkinly in frontline DLBCL, showing a 51% reduction in risk of progression or death. Epkinly's efficacy notably exceeds Roche's Polivy in similar settings, positioning GMAB as a potential market leader among T-cell engagers. Frontline DLBCL represents the key growth driver for Epkinly, and I see upside to the company's $3 billion+ peak sales guidance based on better-than-expected treatment effect.

Seeking Alpha10/6/2026Positive
AbbVie and Genmab Announce Epcoritamab in Combination with R-CHOP Demonstrates Significant Improvement in Progression-Free Survival versus R-CHOP in Patients with Newly Diagnosed Diffuse Large B-Cell Lymphoma

EPCORE DLBCL-2 is the first Phase 3 study of a bispecific antibody combination therapy to demonstrate statistically significant and clinically meaningful improvement in progression-free survival (PFS) in frontline diagnosed diffuse large B-cell lymphoma (DLBCL) patients Based on the topline results, Genmab and AbbVie will engage global regulatory authorities NORTH CHICAGO, Ill. and COPENHAGEN, Denmark, Oct. 5, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV) and Genmab A/S  (Nasdaq: GMAB) today announced positive topline results from the Phase 3 EPCORE DLBCL-2 trial evaluating fixed treatment duration epcoritamab, a T-cell engaging bispecific antibody administered subcutaneously, in combination with standard of care rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine, and prednisone (R-CHOP), compared to R-CHOP alone, in newly diagnosed patients with diffuse large B-cell lymphoma (DLBCL) with an International Prognostic Index (IPI) score of 2 to 5.

PRNewsWire10/5/2026Neutral
Genmab and AbbVie Announce Epcoritamab in Combination with R-CHOP Demonstrates Statistically Significant Improvement in Progression-Free Survival in Patients with Newly Diagnosed Diffuse Large B-Cell Lymphoma

Company Announcement COPENHAGEN, Denmark and NORTH CHICAGO, Ill.; October 5, 2026 EPCORE DLBCL-2 is the first Phase 3 study of a bispecific antibody combination therapy to demonstrate statistically significant and clinically meaningful improvement in progression-free survival (PFS) in frontline diagnosed diffuse large B-cell lymphoma (DLBCL) patients Based on the topline results, Genmab and AbbVie will engage global regulatory authorities Genmab A/S (Nasdaq: GMAB) and AbbVie (NYSE: ABBV) announced today positive topline results from the Phase 3 EPCORE DLBCL-2 trial evaluating fixed treatment duration epcoritamab, a T-cell engaging bispecific antibody administered subcutaneously, in combination with standard of care rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine, and prednisone (R-CHOP), compared to R-CHOP alone, in newly diagnosed patients with diffuse large B-cell lymphoma (DLBCL) with an International Prognostic Index (IPI) score of 2 to 5.

GlobeNewsWire10/5/2026Neutral
Grant of Restricted Stock Units and Warrants to Employees in Genmab

Company Announcement COPENHAGEN, Denmark; September 24, 2026 – Genmab A/S (Nasdaq: GMAB) announced today that the Board of Directors decided to grant 13,794 restricted stock units and 13,331 warrants to employees of the Company and the Company's subsidiaries. Each restricted stock unit is awarded cost-free and provides the owner with a conditional right to receive one share in Genmab A/S of nominally DKK 1.

GlobeNewsWire9/24/2026Neutral

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Data last updated: 10/17/2026