argenx Reports Positive Results for VYVGART in Ocular Myasthenia Gravis Treatment
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 1 hour ago
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Should l Buy ARGX?
Source: Newsfilter
- Clinical Trial Success: argenx's ADAPT OCULUS study met its primary endpoint with a p-value of 0.012, indicating that VYVGART significantly improved Myasthenia Gravis Impairment Index (MGII) Patient Reported Outcomes in patients with ocular myasthenia gravis, showcasing the drug's efficacy and potential market prospects.
- Significant Symptom Improvement: Patients treated with VYVGART showed an average improvement of 4.04 points in MGII PRO scores compared to a 1.99 point improvement in the placebo group, highlighting VYVGART's notable advantage in alleviating ocular symptoms such as diplopia and ptosis, which may attract more patients to the treatment.
- Good Safety Profile: VYVGART was well tolerated in patients with ocular myasthenia gravis, with no new safety concerns identified, consistent with prior studies, which provides confidence for its future market promotion and FDA application.
- Strategic Implications: The study results will support argenx's submission of a Supplemental Biologics License Application (sBLA) to the U.S. FDA to expand VYVGART's indications, addressing the urgent needs of ocular myasthenia gravis patients and further solidifying its leadership position in the autoimmune disease sector.
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Analyst Views on ARGX
Wall Street analysts forecast ARGX stock price to rise
17 Analyst Rating
14 Buy
3 Hold
0 Sell
Strong Buy
Current: 840.280
Low
858.00
Averages
1048
High
1317
Current: 840.280
Low
858.00
Averages
1048
High
1317
About ARGX
argenx SE, formerly arGEN X BV, is a Netherlands-based biopharmaceutical company. It is primarily engaged in creating and developing a pipeline of differentiated antibody therapeutics for the treatment of severe autoimmune diseases using its discovery platform, Simple Antibody, which exploits characteristics of the llama immune system. The Company develops a pipeline of antibody therapeutics focused on cancer and autoimmune indications. It includes, but is not limited to: Empasiprubart, a complement inhibitor targeting C2, blocking the function of both the classical and lectin pathways, while leaving the alternative pathway intact, ARGX-119 an antagonist to the MuSK receptor with potential in multiple neuromuscular indications.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
- Earnings Announcement: argenx SE is set to release its Q4 2023 earnings on February 26 before market open, with consensus EPS estimated at $6.20 and revenue projected at $1.3 billion, reflecting a robust 76.4% year-over-year growth potential in the biopharmaceutical sector.
- Performance Revisions: Over the past three months, EPS estimates have seen 7 upward revisions and 6 downward adjustments, while revenue estimates experienced 8 upward and 9 downward revisions, indicating market divergence regarding the company's future performance, which could impact investor confidence.
- Market Focus: The upcoming earnings report is a focal point for investors, especially against the backdrop of the FDA's priority review of argenx's Vyvgart label expansion, with market expectations high for future product line growth.
- Leadership Transition: argenx recently announced a CEO transition, which may influence the company's strategic direction and market performance, prompting investors to monitor how the new leadership team will drive future growth.
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- Clinical Trial Success: argenx's ADAPT OCULUS study met its primary endpoint with a p-value of 0.012, indicating that VYVGART significantly improved Myasthenia Gravis Impairment Index (MGII) Patient Reported Outcomes in patients with ocular myasthenia gravis, showcasing the drug's efficacy and potential market prospects.
- Significant Symptom Improvement: Patients treated with VYVGART showed an average improvement of 4.04 points in MGII PRO scores compared to a 1.99 point improvement in the placebo group, highlighting VYVGART's notable advantage in alleviating ocular symptoms such as diplopia and ptosis, which may attract more patients to the treatment.
- Good Safety Profile: VYVGART was well tolerated in patients with ocular myasthenia gravis, with no new safety concerns identified, consistent with prior studies, which provides confidence for its future market promotion and FDA application.
- Strategic Implications: The study results will support argenx's submission of a Supplemental Biologics License Application (sBLA) to the U.S. FDA to expand VYVGART's indications, addressing the urgent needs of ocular myasthenia gravis patients and further solidifying its leadership position in the autoimmune disease sector.
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- Earnings Highlights: argenx SE reported a Q4 GAAP EPS of $8.02, exceeding expectations by $1.70, indicating a significant improvement in profitability and reflecting the company's competitive position in the market.
- Revenue Growth: Q4 2025 revenue reached $1.29 billion, a 75% year-over-year increase, although it missed expectations by $10 million, suggesting challenges in the company's rapid expansion.
- Product Sales Performance: VYVGART's net sales for 2025 were $1.3 billion, with annual sales of $4.2 billion, significantly up from $0.7 billion and $2.2 billion in 2024, demonstrating strong market demand.
- FDA Review Progress: The label expansion application for VYVGART is undergoing FDA priority review, and if approved, it will further drive sales growth and enhance the company's market position.
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- Strong Financial Performance: argenx achieved global product net sales of $4.2 billion in 2025, reflecting a remarkable 90% year-over-year growth, with fourth-quarter sales reaching $1.3 billion, indicating robust market expansion and enhanced profitability.
- First Year of Operating Profitability: The company reported $1.1 billion in operating income for 2025, marking its first year of profitability, which underscores successful cost management and market penetration, thereby boosting investor confidence.
- Product Line Expansion: The label expansion of VYVGART is supported by positive results from the ADAPT SERON and OCULUS studies, with a PDUFA target action date of May 10, 2026, for the anti-AChR antibody-negative gMG filing, reinforcing its leadership in the autoimmune disease sector.
- Future Strategic Goals: The company aims to treat 50,000 patients by 2030 and plans to advance five pipeline candidates into Phase 3 development, demonstrating a strong commitment to long-term growth and strategic market expansion.
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- Executive Conference Participation: argenx COO Karen Massey will participate in a fireside chat at the TD Cowen 46th Annual Healthcare Conference on March 2, showcasing the company's advancements in severe autoimmune diseases, which is expected to attract investor and industry attention.
- Live Webcast Arrangement: The presentation will be accessible via a live webcast on the investors section of the argenx website, allowing global investors to obtain real-time information, thereby enhancing the company's transparency and market trust.
- Focus on Innovative Collaboration: argenx is committed to translating immunology breakthroughs into novel antibody-based medicines through its Immunology Innovation Program in partnership with leading academic researchers, demonstrating the company's strategic emphasis on R&D.
- Product Development Outlook: The company is evaluating the broad potential of its first approved FcRn blocker in multiple serious autoimmune diseases, indicating its innovative capabilities and competitive position in the biopharmaceutical sector.
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- Buy Rating Maintained: H.C. Wainwright maintained a Buy rating on Argenx SE (NASDAQ:ARGX) as of January 21, setting a price target of $915, which reflects a modest 8.93% upside from current levels, indicating strong market confidence in its long-term growth potential.
- Price Target Increase: On January 20, Wells Fargo reiterated its Buy rating on Argenx SE while raising its price target from $1,264 to $1,317, implying a further 55% upside from current levels, showcasing analysts' optimism about the company's future performance.
- Revenue Estimates Raised: Wells Fargo also increased its Vyvgart revenue estimates for the 2026-2030 period by 5%-15%, reflecting confidence in stronger-than-expected performance, with a consensus revenue estimate of $5.6 billion for FY 2026, suggesting the market may be underestimating the company's growth potential.
- Growth Potential Analysis: According to Wells Fargo's estimates, Argenx SE could achieve $6.5 billion in revenue by 2026, assuming single-digit quarter-over-quarter growth in Q1, followed by low double-digit growth from Q2 to Q4, further solidifying its market position in the biopharmaceutical sector.
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