| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 2.29B | 2.19B | 1.23B | 410.75M | 497.28M | 41.24M |
| Gross Profit | 1.52B | 1.96B | 1.11B | 381.31M | 497.28M | 41.24M |
| EBITDA | 640.57M | 105.17M | -192.28M | -622.78M | -392.78M | -601.03M |
| Net Income | 1.11B | 833.04M | -295.05M | -709.59M | -407.63M | -608.46M |
Balance Sheet | ||||||
| Total Assets | 7.18B | 6.20B | 4.54B | 3.13B | 2.85B | 2.28B |
| Cash, Cash Equivalents and Short-Term Investments | 3.93B | 3.38B | 3.18B | 2.19B | 2.34B | 2.00B |
| Total Debt | 43.15M | 39.05M | 20.00M | 12.43M | 11.46M | 9.66M |
| Total Liabilities | 1.08B | 704.24M | 444.95M | 320.56M | 316.05M | 605.36M |
| Stockholders Equity | 6.10B | 5.50B | 4.10B | 2.81B | 2.53B | 1.67B |
Cash Flow | ||||||
| Free Cash Flow | 473.52M | -151.05M | -464.14M | -966.63M | -728.25M | -403.60M |
| Operating Cash Flow | 479.76M | -82.75M | -420.33M | -862.81M | -606.81M | -398.46M |
| Investing Cash Flow | -214.14M | -717.59M | 308.21M | -461.18M | -347.07M | 344.69M |
| Financing Cash Flow | 313.76M | 279.76M | 1.34B | 843.76M | 1.12B | 833.00M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
82 Outperform | $79.26B | 18.05 | 15.19% | 0.45% | 2.89% | 0.50% | |
81 Outperform | $20.80B | 17.77 | 30.39% | ― | 18.09% | 3563.21% | |
79 Outperform | $49.76B | 37.55 | 24.75% | ― | 89.58% | ― | |
76 Outperform | $21.59B | 14.89 | 28.20% | ― | 24.98% | 127.06% | |
60 Neutral | $48.47B | 1,526.04 | 32.73% | ― | 53.24% | ― | |
53 Neutral | $26.24B | -41.48 | -2.94% | ― | 7.04% | -25.24% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
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.
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.
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.
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.
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.
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.
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.
On October 15, 2025, Argenx SE announced its participation in the 2025 AANEM Annual Meeting and MGFA Scientific Session, where it will present pivotal data on VYVGART and empasiprubart. The company highlighted the potential of VYVGART in treating myasthenia gravis and other neuromuscular diseases, showcasing results from various studies that demonstrate its efficacy and safety. This presentation underscores Argenx’s commitment to advancing innovative therapies and improving patient outcomes in the field of autoimmune and neuromuscular diseases.
The most recent analyst rating on (ARGX) stock is a Buy with a $800.00 price target. To see the full list of analyst forecasts on Argenx Se stock, see the ARGX Stock Forecast page.