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GMAB Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
29.410
Open
29.070
VWAP
29.10
Vol
1.13M
Mkt Cap
17.20B
Low
28.830
Amount
32.75M
EV/EBITDA(TTM)
15.32
Total Shares
613.94M
EV
21.27B
EV/OCF(TTM)
23.58
P/S(TTM)
4.50
Genmab A/S is a Denmark-based international biotechnology company. It specializes in the creation and development of antibody therapeutics for the treatment of cancer. The Company is the creator of the approved antibodies: DARZALEX (daratumumab) for the treatment of certain multiple myeloma indications, Kesimpta for the treatment of adults with relapsing forms of multiple sclerosis, TEPEZZA (teprotumumab) for the treatment of thyroid eye disease and FASPRO, for the treatment of adult patients with certain multiple myeloma indications. The first approved Genmab created therapy Arzerra, approved for the treatment of certain chronic lymphocytic leukemia indications, is available in Japan and is also available in other territories via compassionate use or oncology access programs. Genmab develops a broad clinical and pre-clinical product pipeline, and owns four antibody technologies, DuoBody bispecific platform, HexaBody platform, DuoHexaBody platform & HexElect platform.
Show More

Events Timeline

(ET)
2026-07-06
14:00:00
Genmab Receives Approval for TEPKINLY in Combination Therapy for Relapsed Follicular Lymphoma
select
2026-06-29 (ET)
2026-06-29
16:30:00
Genmab EPCORE DLBCL-4 Trial Results Significantly Improve Survival Rates
select
2026-06-29
16:30:00
Genmab Reports Significant Results from EPCORE DLBCL-4 Trial
select
2026-06-29
16:30:00
AbbVie Reports Positive Results from EPCORE DLBCL-4 Trial
select
2026-06-14 (ET)
2026-06-14
17:30:00
Genmab Reports New Epcoritamab Data, 93% ORR in Elderly DLBCL Patients
select

News

NASDAQ.COM
9.0
09:04 AMNASDAQ.COM
PinnedGenmab's TEPKINLY Approved by EU for Follicular Lymphoma
  • Therapy Approval: Genmab A/S announced that the European Commission has approved TEPKINLY (epcoritamab) in combination with lenalidomide and rituximab, marking a significant breakthrough as the first bispecific therapy for relapsed or refractory follicular lymphoma.
  • Clinical Trial Results: Based on the EPCORE FL-1 trial results, TEPKINLY + R2 demonstrated a 79% reduction in the risk of disease progression or death (HR 0.21, p<0.0001), with overall response rates reaching 96%, significantly higher than the 81% seen with R2 alone, indicating its clinical significance.
  • Treatment Paradigm Shift: TEPKINLY + R2 offers a chemotherapy-free treatment option that may change the treatment paradigm for follicular lymphoma, particularly for patients facing recurrent relapses, providing more durable responses and improving quality of life.
  • Safety Profile: The safety profile of the combination was consistent with known effects of epcoritamab and R2, with 44% of patients experiencing serious adverse events, including common reactions like neutropenia, rash, and fatigue, necessitating close monitoring in clinical applications.
Newsfilter
8.5
07-06Newsfilter
PinnedTEPKINLY® Approved in Europe for Relapsed Follicular Lymphoma Treatment
  • Clinical Trial Results: The Phase 3 EPCORE®FL-1 trial demonstrated a 79% reduction in the risk of disease progression or death with TEPKINLY + R2, indicating significant efficacy in treating relapsed follicular lymphoma and the potential to change existing treatment paradigms.
  • Efficacy Data: The overall response rate for TEPKINLY + R2 reached 96%, compared to 81% for R2 alone, highlighting a higher complete response rate of 74% among patients treated with TEPKINLY, showcasing its potential clinical value.
  • Safety Analysis: The safety profile of TEPKINLY + R2 in the EPCORE FL-1 study was consistent with known profiles of individual regimens, with 44% of patients experiencing serious adverse reactions, but management and monitoring measures provided safety assurance for patients.
  • Market Impact: The approval of TEPKINLY offers a new treatment option for patients with relapsed follicular lymphoma, particularly at first relapse, which could significantly improve patient quality of life and enhance Genmab's market position in oncology.
seekingalpha
9.0
17:11 PMseekingalpha
European Commission Approves Tepkinly Label Expansion for Blood Cancer Therapy
  • Label Expansion Approved: The European Commission has authorized Tepkinly as a first-line treatment option for patients with relapsed or refractory follicular lymphoma, marking its legalization across 27 EU member states, Norway, Iceland, and Liechtenstein.
  • Clinical Trial Support: This approval is backed by data from AbbVie and Genmab's Phase 3 EPCORE FL-1 trial, demonstrating significant advantages in treatment efficacy for the bispecific antibody therapy, further solidifying its market position.
  • Growing Market Demand: Follicular lymphoma has a higher prevalence in Europe, with rates ranging from 11%-29%, compared to 2%-18% in other regions, indicating substantial market potential for Tepkinly to meet the increasing patient demand.
  • Previous Approval Context: Tepkinly was previously approved in the U.S. under the brand name Epkinly as a monotherapy for patients with diffuse large B-cell lymphoma and relapsed follicular lymphoma who had undergone at least two prior lines of systemic therapy, showcasing its broad applicability across different indications.
Yahoo Finance
8.5
09:04 AMYahoo Finance
Genmab's Tepkinly Approved by European Commission
  • Drug Approval: Genmab announced that its cancer drug Tepkinly, in combination with lenalidomide, has been approved by the European Commission, marking a significant milestone that will strongly support the company's market expansion in cancer treatment.
  • Market Potential: The approval of Tepkinly is expected to significantly enhance Genmab's revenue potential, particularly in the European market, addressing the growing patient demand and strengthening the company's competitive position in the biopharmaceutical industry.
  • Strategic Partnerships: This approval lays the groundwork for potential collaborations between Genmab and other pharmaceutical companies, further driving its global business development and innovation capabilities.
  • Investor Confidence: This approval news is likely to boost investor confidence in Genmab, with expectations of a positive impact on its stock price, reflecting the market's optimistic outlook on its future growth prospects.
seekingalpha
9.0
06-29seekingalpha
AbbVie's Epkinly Shows Significant Survival Benefits in Lymphoma Patients
  • Clinical Trial Results: AbbVie's experimental T-cell engaging bispecific antibody Epkinly (epcoritamab) combined with Revlimid (lenalidomide) demonstrated significant improvements in progression-free survival for large B-cell lymphoma patients, reducing disease progression and death by 60% and 56%, respectively, compared to the control group receiving Rituxan (rituximab), gemcitabine, and oxaliplatin.
  • Significant Treatment Impact: The phase 3 EPCOREDLBCL-4 trial results indicate that patients in the Epkinly group experienced markedly lower rates of disease progression and mortality, providing a new treatment option that could potentially redefine the standard of care for large B-cell lymphoma.
  • Market Potential: With Epkinly approved for third-line treatment of large B-cell lymphoma, its combination with Revlimid may attract increased attention from clinicians, thereby driving AbbVie's market share growth in this therapeutic area.
  • Strategic Partnership: AbbVie markets Epkinly in collaboration with Genmab (GMAB), a partnership that not only enhances both companies' competitive positions in the biopharmaceutical sector but also lays the groundwork for future joint research and market expansion efforts.
Yahoo Finance
9.0
06-29Yahoo Finance
Genmab Phase 3 Study Success
  • Clinical Trial Success: Genmab announced that its Phase 3 study of epcoritamab combined with lenalidomide successfully met its primary endpoint, demonstrating the efficacy of this combination in treating specific cancer types, potentially offering new treatment options for patients.
  • Significant Market Potential: The success of this study not only enhances Genmab's competitive position in the market but may also increase its share in the global oncology treatment market, likely attracting more investor interest.
  • Future Development Plans: Genmab plans to submit regulatory applications in the coming months, and if approved, this will accelerate the commercialization process of the therapy, leading to substantial revenue growth for the company.
  • Strategic Collaboration Opportunities: This success opens up potential collaboration opportunities between Genmab and pharmaceutical companies, which could lead to more R&D partnerships and market promotions, further strengthening its influence in the biopharmaceutical sector.
Wall Street analysts forecast GMAB stock price to rise
7 Analyst Rating
Wall Street analysts forecast GMAB stock price to rise
5 Buy
2 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
26.00
Averages
38.50
High
48.00
Current: 0.000
sliders
Low
26.00
Averages
38.50
High
48.00
H.C. Wainwright
Raghuram Selvaraju
Buy
maintain
$38 -> $40
AI Analysis
2026-07-02
New
Reason
H.C. Wainwright
Raghuram Selvaraju
Price Target
$38 -> $40
AI Analysis
2026-07-02
New
maintain
Buy
Reason
H.C. Wainwright analyst Raghuram Selvaraju raised the firm's price target on Genmab to $40 from $38 and keeps a Buy rating on the shares after the company announced that the EPCORE DLBCL-4 trial met its primary objective. The firm increased the probability of approval for Epkinly in both the first- and second-line setting to 70% and 95%, respectively.
Truist
Gregory Renza
Buy
to
Strong Buy
downgrade
$48 -> $40
2026-05-27
Reason
Truist
Gregory Renza
Price Target
$48 -> $40
2026-05-27
downgrade
Buy
to
Strong Buy
Reason
Truist analyst Gregory Renza assumed coverage of Genmab with a Buy rating and a price target of $40, down from $48. The firm is positive on the company's transition toward a commercially driven platform, supported by three lead assets with up to seven key readouts in 2026, the analyst tells investors in a research note. Epkinly's DLBCL-2/-4 outcomes are pivotal for franchise expansion, with Rina-S and petosemtamab carrying potential for best-/first-in-class positioning in ovarian cancer and HNSCC, respectively, the firm added.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for GMAB
Unlock Now

Valuation Metrics

The current forward P/E ratio for Genmab A/S (GMAB.O) is 16.92, compared to its 5-year average forward P/E of 31.63. For a more detailed relative valuation and DCF analysis to assess Genmab A/S's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PE
31.63
Current PE
16.92
Overvalued PE
52.66
Undervalued PE
10.60

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
22.55
Current EV/EBITDA
2.59
Overvalued EV/EBITDA
47.45
Undervalued EV/EBITDA
-2.35

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
8.15
Current PS
0.54
Overvalued PS
13.47
Undervalued PS
2.83

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Whales Holding GMAB

P
Paradigm Biocapital Advisors LP
Holding
GMAB
+27.92%
3M Return
E
Evli Fund Management Company Ltd.
Holding
GMAB
+14.77%
3M Return
U
Union Bancaire Privée, UBP SA
Holding
GMAB
+7.95%
3M Return
B
Baillie Gifford
Holding
GMAB
+7.90%
3M Return
H
Harding Loevner LP
Holding
GMAB
+5.11%
3M Return
F
Folketrygdfondet
Holding
GMAB
-8.01%
3M Return

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Frequently Asked Questions

What is Genmab A/S (GMAB) stock price today?

The current price of GMAB is 29.05 USD — it has increased 3.71

What is Genmab A/S (GMAB)'s business?

Genmab A/S is a Denmark-based international biotechnology company. It specializes in the creation and development of antibody therapeutics for the treatment of cancer. The Company is the creator of the approved antibodies: DARZALEX (daratumumab) for the treatment of certain multiple myeloma indications, Kesimpta for the treatment of adults with relapsing forms of multiple sclerosis, TEPEZZA (teprotumumab) for the treatment of thyroid eye disease and FASPRO, for the treatment of adult patients with certain multiple myeloma indications. The first approved Genmab created therapy Arzerra, approved for the treatment of certain chronic lymphocytic leukemia indications, is available in Japan and is also available in other territories via compassionate use or oncology access programs. Genmab develops a broad clinical and pre-clinical product pipeline, and owns four antibody technologies, DuoBody bispecific platform, HexaBody platform, DuoHexaBody platform & HexElect platform.

What is the price predicton of GMAB Stock?

Wall Street analysts forecast GMAB stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for GMAB is38.50 USD with a low forecast of 26.00 USD and a high forecast of 48.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Genmab A/S (GMAB)'s revenue for the last quarter?

Genmab A/S revenue for the last quarter amounts to 896.00M USD, increased 25.31

What is Genmab A/S (GMAB)'s earnings per share (EPS) for the last quarter?

Genmab A/S. EPS for the last quarter amounts to 0.83 USD, decreased -72.79

How many employees does Genmab A/S (GMAB). have?

Genmab A/S (GMAB) has 3029 emplpoyees as of July 07 2026.

What is Genmab A/S (GMAB) market cap?

Today GMAB has the market capitalization of 17.20B USD.