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Genmab A/S (GMAB)
NASDAQ:GMAB

Genmab (GMAB) AI Stock Analysis

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GMAB

Genmab

(NASDAQ:GMAB)

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Neutral 66 (OpenAI - 5.2)
Rating:66Neutral
Price Target:
$32.00
▲(8.70% Upside)
Action:DowngradedDate:02/24/26
The score is supported by strong financial performance (rapid growth, high margins, solid cash generation) and a constructive earnings outlook with meaningful pipeline catalysts, but is held back by the sharp 2025 leverage increase and weaker earnings quality signals, plus bearish near-term technical momentum despite oversold readings.
Positive Factors
Cash generation & FCF conversion
Consistent, strong operating cash flow and near‑par free cash flow conversion provide durable internal funding for R&D, launches, deleveraging and buybacks. This cash resilience reduces reliance on external financing and supports multi-year investment and capital allocation plans.
Proprietary product momentum
Rapid, repeatable growth from proprietary medicines diversifies revenue beyond royalties and demonstrates commercial execution. Durable uptake across markets and expanding indications underpin longer-term revenue streams and lower partner-dependency as Genmab shifts to a partially integrated commercial model.
Strategic pipeline expansion (Merus)
Bolt-on acquisition adds a late‑stage, high‑impact asset and accelerates Genmab’s transition to a broader oncology franchise. Petosemtamab’s encouraging data and regulatory designations materially deepen the launch pipeline and increase multi‑year upside from new product introductions.
Negative Factors
Sharp increase in leverage
Material step-up in leverage reduces balance sheet flexibility and raises interest expense sensitivity. Higher gross leverage increases refinancing and covenant risk over a multi-year horizon, constraining nimble capital allocation until stated deleveraging targets are achieved.
Regulatory/clinical uncertainty (EPKINLY)
An OS miss introduces durable regulatory and label risk that can limit indication expansion and peak sales. Agency discussions, potential confirmatory trials and constrained labeling could delay or reduce the long‑term commercial potential of a core bispecific franchise.
Margin & earnings quality pressure
Rising operating expenses for launches and increased financing costs compressed net margin and weakened OCF coverage, signaling timing or working‑capital pressures. Persisting margin erosion would impede deleveraging and reduce internally available funds for sustained pipeline investment.

Genmab (GMAB) vs. SPDR S&P 500 ETF (SPY)

Genmab Business Overview & Revenue Model

Company DescriptionGenmab 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.
How the Company Makes MoneyGenmab generates revenue primarily through collaborations and partnerships with major pharmaceutical companies, where it receives upfront payments, milestone payments based on the progress of drug development, and royalties on sales of commercialized products. The company has significant collaborations with firms such as Johnson & Johnson and AbbVie, which contribute to its earnings through shared development costs and revenue from successful products. Additionally, Genmab also earns revenue from the sale of its own proprietary products, such as Darzalex (daratumumab), which is marketed for multiple myeloma, contributing to a steady stream of income from sales. These diverse revenue streams, including both collaboration agreements and product sales, form the backbone of Genmab's financial model.

Genmab Earnings Call Summary

Earnings Call Date:Feb 17, 2026
(Q4-2025)
|
% Change Since: |
Next Earnings Date:May 07, 2026
Earnings Call Sentiment Positive
The call highlighted strong commercial execution and financial performance in 2025 — including 19% total revenue growth to $3.7B, substantial proprietary product momentum (EPKINLY +67% to $468M; TIVDAK +26% to $164M), operating profit expansion to $1.26B, and strategic pipeline enhancement via the Merus acquisition (petosemtamab). Management outlined multiple near‑term clinical catalysts (up to six potential registrational readouts in 2026) and a disciplined capital allocation plan, while also acknowledging important challenges: a Phase III EPKINLY monotherapy study where OS missed statistical significance (confounded by COVID and evolving treatment landscape), higher operating expenses to fund launches and development (+13%), and increased leverage and financing costs following the acquisition. Overall, the positives — durable revenue and product growth, a deeper late‑stage pipeline with compelling early data, and clear guidance on investments and deleveraging — materially outweigh the clinical and financing risks discussed, although these risks warrant monitoring as the 2026 readouts and regulatory interactions unfold.
Q4-2025 Updates
Positive Updates
Strong Revenue Growth
Total revenue increased 19% year-over-year to $3.7 billion in FY2025, reflecting growth across royalty streams and commercialized medicines.
Rapid Growth of Proprietary Medicines
Sales of Genmab's proprietary medicines totaled $632 million, up 54% year-over-year and accounting for ~28% of total revenue growth.
EPKINLY Commercial Momentum
EPKINLY generated $468 million in sales in 2025, a 67% year-over-year increase; approved in more than 65 countries and positioned as a dual-indication bispecific across DLBCL and follicular lymphoma.
TIVDAK Market Traction
TIVDAK sales reached $164 million in 2025, up 26% year-over-year, with approvals in the EU, U.K., Japan and continued U.S. growth as a standard of care in recurrent/metastatic cervical cancer.
Improved Profitability
Operating profit expanded to $1.26 billion in 2025 despite strategic investments, demonstrating operating leverage as the business scales.
Bolt-on Acquisition Strengthening Late‑Stage Pipeline
Merus acquisition added petosemtamab to Genmab's late-stage portfolio, expanding high-impact assets alongside EPKINLY and Rina-S and increasing potential future launch catalysts.
Compelling Early Clinical Data for Petosemtamab
In first-line head and neck cancer, petosemtamab plus pembrolizumab achieved a 63% response rate, versus ~19% with standard of care—supporting multibillion-dollar potential.
Robust Late‑Stage Pipeline and Regulatory Recognition
Three late-stage programs (EPKINLY, Rina-S, petosemtamab) hold five combined breakthrough therapy designations; company expects up to six potentially registrational data readouts in 2026 that could enable 2027 launches.
Guidance and Capital Allocation Discipline
2026 midpoint guidance anticipates ~14% revenue growth and $1.15 billion operating profit at midpoint while reaffirming capital allocation priorities, pipeline investment, and a target to reduce gross leverage below 3x by end of 2027.
Debt Financing Completed
Completed a $5.5 billion debt offering ($2.5B fixed, $3.0B floating) with ~$1.6B of the floating portion hedged to fixed (net ~$4.1B fixed) to support the Merus acquisition and integration.
Negative Updates
EPCORE DLBCL‑1: OS Did Not Reach Statistical Significance
The Phase III EPCORE DLBCL‑1 trial showed improvement in progression‑free survival and response metrics for EPKINLY monotherapy but overall survival did not reach statistical significance, introducing regulatory uncertainty and the need for further agency discussions.
Clinical Readout Confounders and Regulatory Risk
Management cited confounding factors (notably the Omicron COVID wave and changing access to other bispecifics) as contributors to trial outcomes, increasing complexity in regulatory discussions and confirmatory study planning.
Increased Operating Expenses
Operating expenses increased ~13% in 2025 due to strategic investments in commercialization and late‑stage development, contributing to a planned step-up in 2026 OpEx to fund petosemtamab and Rina‑S activities.
Near‑Term Profit Guidance Below 2025 Levels at Midpoint
2026 guidance midpoint projects $1.15 billion operating profit versus $1.26 billion in 2025, reflecting reinvestment into growth even as management emphasizes maintained profitability discipline.
Leverage and Financing Costs
Post‑acquisition financing increases gross leverage near-term; weighted average effective interest on the debt package cited around ~6.6%, underscoring the importance of the stated deleveraging plan to get below 3x gross leverage by end of 2027.
Regulatory Paths Dependent on Additional Readouts
Rina‑S relies on a pivotal Phase II (ORR and DoR) for accelerated pathways with required confirmatory Phase IIIs; multiple pivotal programs have readouts expected in 2026 but timing uncertainties and event‑tracking details remain limited.
Competitive and Execution Risks
Market competition (other bispecifics, ADCs, PD‑1 combinations like recent pembrolizumab approvals) and integration execution risks for Merus create potential headwinds to uptake and labeling strategy.
Company Guidance
Genmab's 2026 guidance targets total revenue growth of about 14% at the midpoint (building on 2025 revenue of $3.7B, +19% YoY), with DARZALEX net sales expected at $15.6–16.4B and operating profit of $1.15B at the midpoint (2025 operating profit was $1.26B); the company will increase operating investments to advance petosemtamab and Rina‑S and support launch readiness (OpEx rose 13% in 2025) while maintaining substantial profitability and targeting gross leverage below 3x by end‑2027. Genmab closed a $5.5B debt raise (≈$2.5B fixed, $3.0B floating with ~$1.6B hedged, net ≈$4.1B fixed) at a weighted average effective rate near 6.6%. The guidance is underpinned by commercial momentum—2025 proprietary medicine sales of $632M (+54% YoY, ~28% of total revenue growth), EPKINLY $468M (+67% YoY) and TIVDAK $164M (+26% YoY)—and by up to six potential registrational data readouts in 2026 that could materially expand addressable populations (e.g., EPKINLY from ~27,000 today toward ~150,000 by the early 2030s).

Genmab Financial Statement Overview

Summary
Strong revenue acceleration (~69% growth in 2025) and very high gross margin (~91.7%) support a solid profitability profile, with robust and consistent operating cash flow and strong free-cash-flow conversion. Offsetting this, 2025 introduced higher risk: leverage rose sharply (debt-to-equity ~0.95), net margin declined (~36.4% to ~25.9%), and operating cash flow covered net income less than 1x (~0.83x), pointing to weaker earnings quality/timing pressures.
Income Statement
86
Very Positive
GMAB shows strong top-line momentum, with revenue accelerating to ~69.0% growth in 2025 versus more modest growth in 2023–2024. Profitability remains high with very strong gross margins (still ~91.7% in 2025) and solid operating profitability (2025 EBIT margin ~33.6%). The key weakness is volatility in bottom-line efficiency: net margin fell to ~25.9% in 2025 from ~36.4% in 2024, despite higher revenue, indicating higher costs and/or non-operating headwinds impacting earnings quality year-over-year.
Balance Sheet
62
Positive
The balance sheet was very conservatively levered from 2020–2024 (debt-to-equity ~0.02–0.03), supported by a growing equity base. However, 2025 marks a notable shift: total debt jumped materially and debt-to-equity rose to ~0.95, which meaningfully increases financial risk and reduces balance-sheet flexibility versus prior years. While equity remains sizable, the step-change in leverage is the primary concern.
Cash Flow
78
Positive
Cash generation is strong and consistent, with operating cash flow remaining robust (roughly 7.4–7.8B in 2023–2025) and free cash flow closely tracking net income (free cash flow to net income ~0.97 in 2025), suggesting good earnings-to-cash conversion. Free cash flow growth was exceptional in 2025 (~151.9%), but a key watch item is that operating cash flow covered net income less than 1x in 2025 (~0.83x) versus comfortably above 1x in prior years, pointing to some near-term working-capital or timing pressure.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue23.73B21.53B16.47B14.51B8.42B
Gross Profit21.76B20.54B16.25B14.51B8.42B
EBITDA8.43B9.70B5.95B7.35B4.18B
Net Income6.14B7.84B4.35B5.45B2.96B
Balance Sheet
Total Assets81.86B45.81B35.29B30.12B24.63B
Cash, Cash Equivalents and Short-Term Investments10.91B21.10B28.14B22.32B19.34B
Total Debt35.36B1.03B770.00M597.00M425.00M
Total Liabilities44.68B9.11B3.68B2.84B2.43B
Stockholders Equity37.18B36.70B31.61B27.28B22.20B
Cash Flow
Free Cash Flow7.33B7.58B7.00B3.60B1.98B
Operating Cash Flow7.56B7.77B7.38B3.91B2.23B
Investing Cash Flow-35.99B-9.91B-1.28B-2.76B-961.00M
Financing Cash Flow30.55B-3.92B-606.00M-789.00M-420.00M

Genmab Technical Analysis

Technical Analysis Sentiment
Neutral
Last Price29.44
Price Trends
50DMA
31.93
Negative
100DMA
31.38
Negative
200DMA
27.47
Positive
Market Momentum
MACD
-0.87
Positive
RSI
38.85
Neutral
STOCH
37.71
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For GMAB, the sentiment is Neutral. The current price of 29.44 is below the 20-day moving average (MA) of 30.39, below the 50-day MA of 31.93, and above the 200-day MA of 27.47, indicating a neutral trend. The MACD of -0.87 indicates Positive momentum. The RSI at 38.85 is Neutral, neither overbought nor oversold. The STOCH value of 37.71 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Neutral sentiment for GMAB.

Genmab Risk Analysis

Genmab disclosed 51 risk factors in its most recent earnings report. Genmab reported the most risks in the "Legal & Regulatory" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Genmab Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
83
Outperform
$20.15B15.8229.87%18.09%3563.21%
75
Outperform
$26.66B25.9411.48%2.23%3.72%-31.46%
74
Outperform
$11.87B34.645.94%12.31%60.21%
66
Neutral
$18.00B18.8817.65%24.98%127.06%
57
Neutral
$14.33B-55.63103.32%47.55%
53
Neutral
$26.51B-41.92-2.94%7.04%-25.24%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
GMAB
Genmab
29.44
6.48
28.22%
BMRN
BioMarin Pharmaceutical
61.73
-9.29
-13.08%
INCY
Incyte
101.27
31.01
44.14%
ASND
Ascendis Pharma
233.50
81.57
53.69%
BNTX
BioNTech SE
110.23
-1.33
-1.19%
RPRX
Royalty Pharma
46.21
13.14
39.72%

Genmab Corporate Events

Genmab Reports Initial Transactions Under February 2026 Share Buy-back Program
Feb 23, 2026

Genmab A/S, the Copenhagen-headquartered biotech group specializing in antibody-based therapies for cancer and serious diseases, operates across North America, Europe and Asia Pacific and has eight approved antibody medicines backed by a robust late-stage clinical pipeline. Its platforms span bispecific antibodies, antibody–drug conjugates and other next-generation modalities targeting transformative treatments.

On February 23, 2026, Genmab reported initial transactions under a share buy-back program launched on February 17, 2026 to repurchase up to 342,130 shares for up to DKK 725 million to meet Restricted Stock Unit obligations. Between February 18 and 20, 2026, the company bought 63,000 shares for a total of DKK 115.2 million, lifting its treasury position to 2,678,851 shares, or 4.17% of share capital, signaling ongoing capital management while remaining within EU market abuse “safe harbour” rules.

The most recent analyst rating on (GMAB) stock is a Buy with a $40.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Discloses CFO Insider Share Sale Under EU Market Abuse Rules
Feb 20, 2026

On February 20, 2026, Genmab A/S reported insider share transactions by a senior executive, complying with European market abuse regulations. The disclosure underscores the company’s adherence to transparency rules governing trading by managerial employees and their closely associated persons.

The filing details that Executive Vice President and Chief Financial Officer Anthony Pagano sold a total of 1,100 Genmab shares on February 19, 2026, on Nasdaq Copenhagen at an average price of DKK 1,810.10. While modest in size, the trade is formally reported under Article 19 of the Market Abuse Regulation, providing investors and regulators with timely visibility into management dealings in the stock.

The most recent analyst rating on (GMAB) stock is a Hold with a $34.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Calls March 19 AGM to Approve 2025 Results and Capital Reduction
Feb 18, 2026

Genmab A/S has convened its 2026 Annual General Meeting for March 19, 2026, at the Copenhagen Marriott Hotel, where shareholders will review 2025 performance, vote on the audited annual report and compensation report, and consider board and auditor elections. The board proposes carrying forward the 2025 profit of USD 963 million to retained earnings, maintaining 2026 board and committee fees at 2025 levels, and re-electing six directors, preserving a diverse and largely independent board while also seeking approval to reduce share capital via cancellation of treasury shares, which would modestly enhance capital structure efficiency and per-share metrics.

Shareholders will also vote on reappointing Deloitte as auditor, including a limited assurance mandate on sustainability statements, underscoring Genmab’s focus on governance and ESG disclosure. The meeting agenda, including authorization of the chair to implement resolutions, reflects a continuation of the company’s current strategic and governance framework, with no major shifts in capital allocation but a clear emphasis on stability, board continuity and incremental capital optimization through the proposed share capital reduction.

The most recent analyst rating on (GMAB) stock is a Hold with a $34.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Launches DKK 725 Million Share Buy-Back to Cover RSU Commitments
Feb 17, 2026

Genmab A/S, the Copenhagen-based biotechnology group specializing in antibody medicines for oncology and other serious illnesses, has built a portfolio that includes bispecific antibodies, antibody-drug conjugates and immune-modulating antibodies. The company’s science underpins eight approved antibody drugs and supports a late-stage clinical pipeline of both partnered and wholly owned programs targeting transformative treatments.

On February 17, 2026, Genmab announced the launch of a share buy-back program to meet obligations under its Restricted Stock Unit scheme. Beginning February 18 and running no later than March 31, 2026, the company may repurchase up to 342,130 shares for a maximum of 725 million DKK via Danske Bank under a non-discretionary mandate, a move that modestly increases potential capital returns while managing dilution and adds to the 2,615,851 treasury shares already held.

The buy-back will be executed on Nasdaq Copenhagen and other multilateral trading facilities in line with EU “Safe Harbour” rules governing price and volume, including daily caps tied to recent trading volumes. Genmab retains the right to suspend or terminate the program and will provide weekly disclosures on repurchases, offering investors transparency on execution and the pace of treasury share accumulation supporting its equity compensation strategy.

The most recent analyst rating on (GMAB) stock is a Hold with a $34.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Updates Articles of Association to Expand Capital-Raising and Incentive Flexibility
Feb 3, 2026

On February 3, 2026, Genmab A/S filed a Form 6-K in the United States detailing an updated set of Articles of Association adopted on January 29, 2026, which formalize key elements of the company’s corporate structure and capital framework. The revised articles confirm the company’s current share capital of DKK 64,238,408 and grant the board authority, through March 12, 2029, to increase share capital by up to a nominal DKK 6.6 million with or without pre-emptive rights, issue warrants and convertible debt for employees and investors under specified caps, and adjust the articles accordingly, measures that collectively give management material flexibility to fund growth and incentivize staff while potentially diluting existing shareholders over time.

The most recent analyst rating on (GMAB) stock is a Buy with a $38.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Grants New RSUs and Warrants to Employees to Strengthen Long-Term Incentives
Jan 29, 2026

On January 29, 2026, Genmab A/S announced that its board had granted 32,806 restricted stock units and 34,307 warrants to employees of the company and its subsidiaries as part of its long-term incentive programs. The RSUs, each representing the conditional right to one Genmab share with a fair value equal to the January 29 closing price of DKK 2,067, will vest after three years subject to program conditions, while the cost-free warrants, also struck at DKK 2,067 per share and valued at DKK 658.81 using Black-Scholes, will vest after three years and remain exercisable until seven years from the grant date. The move underscores Genmab’s continued use of equity-based compensation to align employees with shareholder interests and support retention in a competitive global biotech talent market.

The most recent analyst rating on (GMAB) stock is a Buy with a $38.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Reports 2025 DARZALEX Net Sales of USD 14.4 Billion
Jan 21, 2026

On January 21, 2026, Genmab reported that 2025 worldwide net trade sales of the multiple myeloma therapy DARZALEX (daratumumab), including its subcutaneous formulation DARZALEX FASPRO, reached USD 14.351 billion, according to figures from license partner Johnson & Johnson’s Janssen unit. Sales totaled USD 8.266 billion in the United States and USD 6.085 billion in the rest of the world, and Genmab earns royalties on all global DARZALEX sales under its exclusive worldwide license agreement with J&J, underscoring the product’s continued commercial strength and its importance as a major revenue driver for the Danish biotech.

The most recent analyst rating on (GMAB) stock is a Buy with a $39.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Reports Positive Phase 3 Progression-Free Survival Data for Epcoritamab in Relapsed/Refractory DLBCL
Jan 16, 2026

On January 16, 2026, Genmab reported topline Phase 3 results from its global EPCORE DLBCL-1 trial of subcutaneous bispecific antibody epcoritamab in patients with relapsed or refractory diffuse large B‑cell lymphoma who were ineligible for high‑dose chemotherapy and autologous stem cell transplant. The study, which enrolled 483 patients and compared epcoritamab monotherapy with standard chemo‑immunotherapy regimens R‑GemOx or BR, showed a statistically significant improvement in progression‑free survival and gains in complete response rate, duration of response and time to next treatment, while overall survival did not reach statistical significance and safety findings appeared consistent with the known profile. Genmab and partner AbbVie plan to discuss the data with global regulators and continue to position epcoritamab as a potential core therapy across B‑cell malignancies, supported by multiple ongoing Phase 3 programs in both frontline and relapsed DLBCL and follicular lymphoma that could further expand its clinical and commercial footprint if successful.

The most recent analyst rating on (GMAB) stock is a Buy with a $38.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Drops Acasunlimab to Refocus Investment on Late-Stage Cancer Pipeline
Dec 29, 2025

On December 29, 2025, Genmab announced it would discontinue further clinical development of acasunlimab following a portfolio review and assessment of a more competitive market landscape. Although the company described the drug’s clinical profile to date as encouraging, management said it will redirect resources toward late-stage programs it sees as having higher potential impact, notably EPKINLY (epcoritamab), petosemtamab and rinatabart sesutecan (Rina-S). The move underscores Genmab’s disciplined approach to portfolio prioritization and capital allocation, and the company emphasized that the decision will not affect its full-year 2025 financial guidance, reassuring investors that its broader pipeline momentum and financial outlook remain intact.

The most recent analyst rating on (GMAB) stock is a Hold with a $26.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab Completes Acquisition of Merus N.V. to Bolster Oncology Portfolio
Dec 12, 2025

On December 12, 2025, Genmab A/S announced the successful completion of its tender offer to acquire all outstanding common shares of Merus N.V. for $97 per share, marking a significant step in its strategy to become a global biotechnology leader. This acquisition adds petosemtamab, a late-stage asset with two Breakthrough Therapy Designations, to Genmab’s portfolio, and is expected to be accretive to the company’s EBITDA by the end of 2029, with potential multi-billion-dollar annual revenue thereafter.

The most recent analyst rating on (GMAB) stock is a Buy with a $45.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab A/S Discloses Managerial Share Transactions as of December 1, 2025
Dec 1, 2025

On December 1, 2025, Genmab A/S announced transactions involving shares and linked securities conducted by its managerial employees and their closely associated persons. These transactions, which were acquisitions due to the vesting of restricted stock units, reflect internal movements within the company’s stock holdings. The disclosure is in compliance with market regulations and highlights the vested interests of key personnel in Genmab’s operational success.

The most recent analyst rating on (GMAB) stock is a Buy with a $45.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Genmab A/S Updates Articles of Association for Financial Flexibility
Nov 26, 2025

On November 26, 2025, Genmab A/S announced updates to its Articles of Association, which include authorizations for the Board of Directors to increase the company’s share capital and issue warrants and convertible debt instruments. These changes are aimed at providing financial flexibility and supporting the company’s growth strategy, potentially impacting shareholder value and market positioning.

The most recent analyst rating on (GMAB) stock is a Buy with a $45.00 price target. To see the full list of analyst forecasts on Genmab stock, see the GMAB Stock Forecast page.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Feb 24, 2026