tiprankstipranks
Trending News
More News >
Argenx Se (ARGX)
NASDAQ:ARGX

Argenx Se (ARGX) AI Stock Analysis

Compare
756 Followers

Top Page

ARGX

Argenx Se

(NASDAQ:ARGX)

Select Model
Select Model
Select Model
Outperform 79 (OpenAI - 5.2)
Rating:79Outperform
Price Target:
$933.00
▲(14.21% Upside)
Action:ReiteratedDate:11/15/25
Argenx Se's strong financial performance and bullish technical indicators are the primary drivers of its high stock score. The company's robust revenue growth and strategic advancements in its pipeline are significant positives. However, the high valuation and operational challenges in cash flow generation slightly temper the overall score.
Positive Factors
Commercial Momentum (VYVGART)
Rapid commercial adoption of VYVGART, reflected in ~$4.15B preliminary 2025 sales and ~19k patients, creates a durable recurring revenue base. Chronic dosing, growing prescriber penetration and international sales support sustainable top-line growth and fund further label expansion.
Strong Balance Sheet & Low Leverage
Very low leverage and a high equity ratio provide lasting financial flexibility. This structural strength reduces refinancing and liquidity risk, enabling continued investment in manufacturing capacity, commercialization and R&D without near-term solvency pressure.
Advancing Late‑Stage Pipeline
A deep late-stage pipeline with multiple Phase III and planned registrational readouts offers structural growth optionality beyond the lead product. Successful readouts could yield new labeled indications and broaden the addressable market, strengthening long-term revenue diversification.
Negative Factors
Negative Free Cash Flow / Cash Conversion
Persistent negative free cash flow and poor conversion of net income into operating cash indicate structural efficiency issues. Over time this can force reliance on financing, constrain discretionary investments or pressure margins if commercial growth slows or R&D needs rise.
Rising Operating Expenses & Negative EBIT Margin
Increasing R&D and SG&A while EBIT margins remain negative suggests the company must sustain high growth to translate scale into durable profitability. If revenue growth moderates, continued elevated operating spend could limit lasting margin expansion and free cash generation.
Clinical Setbacks and Program Discontinuations
Late‑stage program failures and discontinuations expose pipeline execution risk and can force resource reallocation. Such setbacks reduce the probability of future label expansions, delay potential new revenue streams and increase the importance of fewer remaining programs to long-term growth.

Argenx Se (ARGX) vs. SPDR S&P 500 ETF (SPY)

Argenx Se Business Overview & Revenue Model

Company Descriptionargenx SE, a biotechnology company, engages in the developing of various therapies for the treatment of autoimmune diseases in the United States, Japan, Europe, Middle East, Africa, and China. Its lead product candidate is efgartigimod for the treatment of patients with myasthenia gravis, immune thrombocytopenia, pemphigus vulgaris, generalized myasthenia gravis, chronic inflammatory demyelinating polyneuropathy, thyroid eye disease, bullous pemphigoid, myositis, primary sjögren's syndrome, post-covid postural orthostatic tachycardia syndrome, membranous nephropathy, lupus nephropathy, anca-associated vasculitis, and antibody mediated rejection; ENHANZE SC; Empasiprubart for multifocal motor neuropath, delayed graft function, and dermatomyositis; and ARGX-119 for congenital myasthenic syndrome and amyotrophic lateral sclerosis. The company is developing ARGX-213 targets FcRn; ARGX-121 and ARGX-220 targets immune system; ARGX-109 targets IL-6; ARGX-118 for inflammation; and ARGX-109, as well as cusatuzumab, ARGX-112, ARGX-114, and ARGX-115. It owns VYVGART; VYVGART HYTRULO; VYVDURA; ARGENX; ABDEG; NHANCE; SIMPLE ANTIBODY; and ARGENXMEDHUB. The company has strategic partnership with AbbVie S.À.R.L., Zai Lab Limited, and LEO Pharma A/S; and collaboration and license agreement with Genor Biopharma Co. Ltd, Université Catholique de Louvain, Sopartec S.A., NYU Langone Health, Leiden University Medical Center, AgomAb Therapeutics NV, Broteio Pharma B.V., VIB vzw, University of Texas, BioWa, Inc., and Shire International GmbH. It has collaboration agreement with Genmab A/S to discover, develop, and commercialize novel therapeutic antibodies with applications in immunology and oncology, as well as a strategic collaboration with IQVIA Holdings Inc. to provide safety systems and services. argenx SE was incorporated in 2008 and is based in Amsterdam, the Netherlands.
How the Company Makes MoneyArgenx generates revenue through multiple streams, primarily focused on the commercialization of its therapeutic products. This includes revenue from product sales of its approved therapies, such as efgartigimod, which is marketed for the treatment of autoimmune disorders like myasthenia gravis. Additionally, the company engages in strategic partnerships and collaborations with other pharmaceutical firms, which often involve upfront payments, milestone payments upon achieving certain development or regulatory goals, and royalties on net sales of products developed under these collaborations. These partnerships not only provide financial resources but also enhance Argenx's capabilities in research and development, ultimately contributing to its overall earnings.

Argenx Se Key Performance Indicators (KPIs)

Any
Any
Revenue By Segment
Revenue By Segment
Chart Insights
Data provided by:The Fly

Argenx Se Earnings Call Summary

Earnings Call Date:Feb 26, 2026
(Q4-2025)
|
Next Earnings Date:May 07, 2026
Earnings Call Sentiment Positive
The call presents a strongly positive commercial and financial picture: exceptional revenue growth (+90% YoY), first full-year operating profitability, a robust cash position (+>$1B YoY), and an expanding patient base (≈19,000). Clinically, the positive Phase III ADAPT OCULUS ocular MG readout (p=0.012; mean improvement 4.04 vs 1.99) and recent seronegative data (with a PDUFA in May) materially expand VYVGART’s addressable market and support label expansion. The company also highlighted a deepening pipeline and strategic investments in next-generation FcRn assets. Offsetting factors include a low gross margin (~11%), significant OpEx and R&D spend (combined R&D+SG&A $2.7B; ~30% YoY increase), a failed ALS study that halts that program, regulatory requests increasing trial burden in Graves, and payer/timing uncertainties that could delay realization of some label expansion benefits. Overall, the positive commercial momentum, profitability milestone, and major clinical win for ocular MG outweigh the challenges and near-term risks.
Q4-2025 Updates
Positive Updates
Strong Revenue Growth and Scale
Product net sales of $1.3B in Q4 2025 and $4.2B for full year 2025, representing year-over-year growth of 90%. U.S. Q4 product sales were $1.1B, up 68% year-over-year. Company achieved its first year of annual operating profitability with operating profit of $367M in Q4 and $1.1B for the year, and profit of $533M in Q4 and $1.3B for the full year.
Robust Balance Sheet
Cash, cash equivalents and current financial assets of $4.4B at the end of Q4, representing more than a $1B increase over the year, providing strong capital to invest in commercial expansion and pipeline.
Positive Phase III ADAPT OCULUS Ocular MG Results
Study met primary endpoint (MGII patient‑reported ocular score) with VYVGART Hytrulo showing a mean improvement of 4.04 vs 1.99 for placebo at week 4 (p=0.012). Clear improvements observed in diplopia and ptosis, favorable tolerability and no new safety signals. Company plans to file an sBLA for ocular MG.
Continued MG & CIDP Commercial Momentum
Approximately 19,000 patients on treatment globally at year-end 2025. VYVGART is the fastest-growing and #1 prescribed biologic in MG: 6 out of 10 MG patients starting on a biologic start with VYVGART; 70% of VYVGART patients switched from orals. Prefilled syringe (PFS) launch is a key driver of patient adoption and contributed to >4,700 prescribers (including a dozen new prescribers since PFS launch).
Access Wins Supporting Uptake
Important access win: UnitedHealthcare coverage for the prefilled syringe expanded covered lives to >90%, improving payer access for a key delivery format and supporting adoption in CIDP and MG.
Pipeline Depth and Next-Generation Programs
Advanced immunology pipeline including 4 new molecules from the IIP and next-generation FcRn assets ARGX-213 and ARGX-124. First-in-class candidates progressing (ARGX-121 targeting IgA, ARGX-118 targeting Galectin-10). Company expects to progress 3 Phase I programs in 2026 and has upcoming key readouts including empasiprubart (MMN) readout planned for Q4.
Operational and Strategic Execution
Delivered FY25 combined R&D and SG&A of $2.7B in line with guidance. Management outlines clear strategic priorities (Vision 2030) including label expansions (seronegative PDUFA May 10), new delivery modalities (auto-injector planned for 2027), and a disciplined indication expansion playbook.
Financial Discipline and Tax Position
Year-to-date gross margin ~11% with cost of sales $150M in Q4. Tax for Q4 and full year reflected a net benefit due to nonrecurring items and FX; company expects an effective tax rate in the low- to mid-teens going forward.
Negative Updates
Low Gross Margin
Year-to-date gross margin remains low at approximately 11%, which could limit incremental operating leverage despite strong revenue growth.
Rising Operating Expenses
Total operating expenses in Q4 were $955M (an increase of $149M vs Q3). Combined R&D and SG&A for 2025 totaled $2.7B, ~30% increase over 2024, and management expects continued OpEx growth in 2026 with R&D being the main driver—potential pressure on near-term margins despite revenue growth.
Pipeline Setback in ALS
Phase IIa results for adimanebart in ALS were unsuccessful and do not support progressing in that indication, representing a scientific setback and halted program progression for that asset in ALS.
Regulatory Expectation for Graves Program
Regulatory division requested two trials for the Graves program (instead of a single pivotal), increasing development time and cost and introducing additional regulatory risk.
Payer/Access and Timing Uncertainties
Although ocular MG achieved positive Phase III results, payers previously pushed back on off-label use for ocular presentations; post-approval uptake is expected to require payer discussions and may take ~2 quarters after approval to translate into meaningful coverage changes. Seasonal Q1 dynamics (re-verifications, winter storms) also create near-term revenue variability.
Competitive Landscape and Market Dynamics
Emerging competition in MG (recent approvals by others) could influence market dynamics. Although management is confident in VYVGART’s profile (efficacy, safety, MSE, delivery options), competition adds uncertainty to long-term share and pricing dynamics.
Uncertainties on Next-Gen Timelines
Next-generation assets (e.g., ARGX-213, ARGX-124) are in early stages; timelines for Phase I readouts and registrational paths are not fully specified, leaving timing uncertainty for material upside from these programs.
Company Guidance
Management reiterated clear financial and operating guidance and milestone timing: Q4 product net sales were $1.3B and FY2025 sales $4.2B (up 90% YoY) with Q4 regional sales of $1.1B U.S. (+68% YoY), $63M Japan, $110M rest of world and $26M supplied to Zai Lab; Q4 operating expenses were $955M (up $149M vs Q3), cost of sales $150M, year‑to‑date gross margin 11%, combined R&D+SG&A totaled $2.7B for 2025 (~30% increase vs 2024) and operating profit was $367M in Q4 ($1.1B FY) with net profit of $533M Q4 ($1.3B FY); cash and equivalents were $4.4B (>$1B increase YoY) and the effective tax rate is expected in the low‑to‑mid‑teens. They said OpEx will continue to grow at a similar percentage in 2026 with most incremental spend in R&D, plan to progress three Phase I programs in 2026 and advance next‑gen FcRn assets (ARGX‑213/124) and an auto‑injector in 2027; clinical/commercial milestones include a May 10 PDUFA for seronegative MG, intent to file an sBLA for ocular MG after positive ADAPT OCULUS (141 patients; primary endpoint p=0.012; mean MGII ocular improvement 4.04 vs 1.99), an empasiprubart MMN Q4 readout, ~19,000 patients on VYVGART globally, >4,700 prescribers, PFS coverage >90%, and a U.S. target TAM of ~60,000 (seronegative +11,000; ocular +7,000; CIDP initial ~12,000; IMNM ~20,000).

Argenx Se Financial Statement Overview

Summary
Argenx Se has demonstrated robust revenue growth and improved profitability, supported by a strong balance sheet with minimal leverage. However, challenges in operational efficiency and cash flow generation remain critical areas for improvement.
Income Statement
75
Positive
Argenx Se has shown a significant increase in total revenue from 2023 to 2024, with a revenue growth rate of 77.32%. The company has also improved its profitability, turning a net income of $804 million in 2024 from a net loss of $295 million in 2023. However, the EBIT margin remains negative, indicating ongoing operational challenges.
Balance Sheet
80
Positive
The company's balance sheet is strong, with a high equity ratio of 88.64% and a low debt-to-equity ratio of 0.007. This indicates financial stability and low leverage, reducing financial risk. The return on equity has improved significantly due to positive net income, which enhances shareholder value.
Cash Flow
65
Positive
Argenx Se has managed to improve its free cash flow position slightly, but it remains negative. The operating cash flow to net income ratio is unfavorable, suggesting inefficiencies in converting income into cash flow. However, the company has strong financing activities that continue to support its cash position.
BreakdownTTMDec 2024Dec 2023Dec 2022Dec 2021Dec 2020
Income Statement
Total Revenue2.29B2.19B1.23B410.75M497.28M41.24M
Gross Profit1.52B1.96B1.11B381.31M497.28M41.24M
EBITDA640.57M105.17M-192.28M-622.78M-392.78M-601.03M
Net Income1.11B833.04M-295.05M-709.59M-407.63M-608.46M
Balance Sheet
Total Assets7.18B6.20B4.54B3.13B2.85B2.28B
Cash, Cash Equivalents and Short-Term Investments3.93B3.38B3.18B2.19B2.34B2.00B
Total Debt43.15M39.05M20.00M12.43M11.46M9.66M
Total Liabilities1.08B704.24M444.95M320.56M316.05M605.36M
Stockholders Equity6.10B5.50B4.10B2.81B2.53B1.67B
Cash Flow
Free Cash Flow473.52M-151.05M-464.14M-966.63M-728.25M-403.60M
Operating Cash Flow479.76M-82.75M-420.33M-862.81M-606.81M-398.46M
Investing Cash Flow-214.14M-717.59M308.21M-461.18M-347.07M344.69M
Financing Cash Flow313.76M279.76M1.34B843.76M1.12B833.00M

Argenx Se Technical Analysis

Technical Analysis Sentiment
Negative
Last Price816.95
Price Trends
50DMA
832.20
Negative
100DMA
845.70
Negative
200DMA
736.92
Positive
Market Momentum
MACD
-0.25
Positive
RSI
44.21
Neutral
STOCH
31.07
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For ARGX, the sentiment is Negative. The current price of 816.95 is below the 20-day moving average (MA) of 836.03, below the 50-day MA of 832.20, and above the 200-day MA of 736.92, indicating a neutral trend. The MACD of -0.25 indicates Positive momentum. The RSI at 44.21 is Neutral, neither overbought nor oversold. The STOCH value of 31.07 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for ARGX.

Argenx Se Risk Analysis

Argenx Se disclosed 60 risk factors in its most recent earnings report. Argenx Se reported the most risks in the "Finance & Corporate" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Argenx Se 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
$20.11B15.6129.87%18.09%3563.21%
81
Outperform
$81.62B18.6214.87%0.45%2.89%0.50%
79
Outperform
$51.91B38.3824.75%89.58%
66
Neutral
$18.05B18.7817.65%24.98%127.06%
55
Neutral
$44.14B145.0473.28%53.24%
53
Neutral
$26.66B-41.77-2.94%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
ARGX
Argenx Se
816.95
192.25
30.77%
ALNY
Alnylam Pharma
327.36
90.26
38.07%
INCY
Incyte
99.98
26.80
36.62%
REGN
Regeneron
784.28
85.32
12.21%
GMAB
Genmab
29.29
6.56
28.86%
BNTX
BioNTech SE
109.84
1.04
0.96%

Argenx Se Corporate Events

argenx Wins FDA Priority Review for VYVGART in Seronegative gMG
Jan 13, 2026

On January 13, 2026, argenx SE announced that the U.S. Food and Drug Administration accepted for priority review its supplemental Biologics License Application for intravenous VYVGART (efgartigimod alfa-fcab) to treat adults with acetylcholine receptor antibody seronegative generalized myasthenia gravis, a patient group with high unmet need and no approved options for certain subtypes. The filing, backed by positive Phase 3 ADAPT SERON data showing statistically significant and clinically meaningful improvements in disease activity and a safety profile consistent with prior use, sets a Prescription Drug User Fee Act target action date of May 10, 2026, positioning argenx to potentially broaden VYVGART’s label, strengthen its foothold in the gMG market, and expand its addressable patient population if approval is granted.

The most recent analyst rating on (ARGX) stock is a Hold with a $900.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.

argenx Posts 90% Sales Surge and Maps Pivotal 2026 Pipeline, Leadership Transition
Jan 12, 2026

On January 12, 2026, argenx reported preliminary 2025 global product net sales of $4.15 billion, a 90% year-on-year increase driven by VYVGART, which is now used by roughly 19,000 patients worldwide, and outlined a 2026 plan centered on expanding VYVGART’s use and label, advancing its FcRn franchise, and accelerating its broader immunology pipeline. The company highlighted a pivotal year ahead with four registrational readouts in 2026, including the first Phase 3 data for its C2 antibody empasiprubart, multiple Phase 3 milestones across myasthenia gravis, ITP and rheumatology, and the planned start of additional registrational and early-stage studies that together position argenx for potential new product launches from 2027 onward; it also flagged an upcoming leadership transition, with COO Karen Massey set to become CEO and current CEO Tim Van Hauwermeiren moving to non-executive chairman, underscoring both operational momentum and a managed governance handover for investors and patients.

The most recent analyst rating on (ARGX) stock is a Buy with a $1091.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.

Argenx Unveils CEO Succession as Co‑Founder Moves to Chair Role
Jan 5, 2026

On January 5, 2026, Argenx SE announced a planned leadership transition designed to support its next phase of growth, highlighted by the promotion of Chief Operating Officer Karen Massey to Chief Executive Officer and Executive Director and the move of co-founder and current CEO Tim Van Hauwermeiren to non-executive director and Chairman of the Board, succeeding long-serving chair Peter Verhaeghe, who will retire after serving since 2008. The changes, which remain subject to shareholder approval at the company’s annual general meeting on May 6, 2026, signal a continuity-focused succession that keeps Van Hauwermeiren closely involved in long-term strategy and innovation while elevating Massey, credited with accelerating the launch of flagship product VYVGART and building the company’s commercial engine, to steer execution of Argenx’s Vision 2030 and future expansion, with implications for sustained strategic stability and stakeholder confidence in its growth trajectory.

The most recent analyst rating on (ARGX) stock is a Hold with a $858.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.

argenx Discontinues Phase 3 UplighTED Studies for Thyroid Eye Disease
Dec 15, 2025

On December 15, 2025, argenx SE announced the discontinuation of its Phase 3 UplighTED studies evaluating efgartigimod SC in adults with moderate to severe thyroid eye disease (TED) due to futility, as recommended by an Independent Data Monitoring Committee. Despite the trials not meeting desired outcomes, efgartigimod demonstrated a favorable safety profile. The company plans to conduct a comprehensive analysis of the data to gain insights for future research in TED. This decision reflects argenx’s commitment to responsible resource management in its clinical development programs.

The most recent analyst rating on (ARGX) stock is a Buy with a $1316.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.

argenx SE Shareholders Approve Remuneration Policy at Extraordinary Meeting
Nov 18, 2025

On November 18, 2025, argenx SE announced the approval of its remuneration policy during the Extraordinary General Meeting of shareholders. The policy was approved by a 95.67% majority, with 91.1% of share capital represented, highlighting strong shareholder support and potentially impacting the company’s governance and stakeholder relations.

The most recent analyst rating on (ARGX) stock is a Buy with a $1124.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.

Argenx SE Reports Strong Q3 2025 Financial Results and Strategic Advances
Oct 30, 2025

On October 30, 2025, Argenx SE reported its third quarter financial results, showcasing a significant increase in global product net sales to $1.13 billion, driven by strong demand for VYVGART. The company is on track to submit a supplemental Biologics License Application for VYVGART in seronegative gMG subtypes by year-end and anticipates multiple registrational study readouts in 2026. Argenx is also expanding its manufacturing capabilities in partnership with FUJIFILM, enhancing its supply chain to support future growth. These developments underscore Argenx’s strategic focus on innovation and its Vision 2030 goals, aiming to treat 50,000 patients globally and secure 10 labeled indications across its medicines.

The most recent analyst rating on (ARGX) stock is a Buy with a $943.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.

Argenx SE Highlights VYVGART’s Efficacy in Treating Myasthenia Gravis
Oct 29, 2025

On October 29, 2025, Argenx SE presented new data at the AANEM and MGFA meetings highlighting the efficacy and safety of VYVGART for gMG patients. The data demonstrated significant improvements in patient outcomes, including reduced steroid use and sustained minimal symptom expression, positioning VYVGART as a potentially transformative treatment for gMG across various patient subtypes. These findings underscore VYVGART’s potential to redefine treatment standards and improve quality of life for patients, with plans to seek label expansion to include additional patient subtypes.

The most recent analyst rating on (ARGX) stock is a Buy with a $943.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX 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: Nov 15, 2025