| 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 | 12.50M |
| 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 |
|---|---|---|---|---|---|---|---|
81 Outperform | $21.25B | 17.68 | 30.39% | ― | 18.09% | 3563.21% | |
79 Outperform | $55.73B | 41.89 | 24.75% | ― | 89.58% | ― | |
79 Outperform | $72.89B | 16.60 | 15.19% | 0.40% | 2.89% | 0.50% | |
76 Outperform | $18.85B | 12.74 | 28.20% | ― | 24.98% | 127.06% | |
57 Neutral | $59.81B | 1,888.39 | 32.73% | ― | 53.24% | ― | |
53 Neutral | $26.86B | ― | -2.94% | ― | 7.04% | -25.24% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
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.
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.
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.
On October 3, 2025, Argenx SE announced that it will hold an Extraordinary General Meeting of Shareholders on November 18, 2025, in Amsterdam. The meeting will address the adoption of a revised remuneration policy, and shareholders are encouraged to participate via electronic proxy voting. This meeting is significant for stakeholders as it may impact the company’s governance and strategic direction.
On August 25, 2025, argenx announced positive topline results from its ADAPT SERON study of VYVGART in patients with AChR-Ab seronegative gMG. The study met its primary endpoint, showing significant improvement in patients’ MG-ADL scores, and demonstrated VYVGART’s potential as a targeted treatment across all AChR-Ab seronegative subtypes. The company plans to submit a supplemental Biologics License Application to the FDA by the end of 2025, aiming to expand VYVGART’s label to include these patient subtypes. This advancement highlights argenx’s commitment to addressing the unmet needs of the MG community and could significantly impact its industry positioning.