Argenx SE’s stock price has fluctuated amid regulatory scrutiny over its Vyvgart Hytrulo treatment, but analyst ratings have helped stabilize the stock.
Argenx SE’s approval of its subcutaneous treatment Vyvgart for CIDP has sparked debate over whether it’s a genuine breakthrough or market manipulation.
Argenx SE has secured European Commission approval for its VYVGART subcutaneous injection, a treatment for chronic inflammatory demyelinating polyneuropathy (CIDP), expanding its market reach to 27 EU countries.
Argenx SE has secured European Commission approval for its VYVGART treatment, a major milestone that could lead to significant growth, but investors have yet to take notice.
Argenx presents positive phase 2 proof-of-concept results for its efgartigimod asset in treating myositis and Sjogren’s disease at the EULAR 2025 conference.
Argenx SE has made significant strides in autoimmune disease and cancer therapies, with positive Phase 2 results for its efgartigimod treatment and FDA Fast Track designation for Sjogren’s disease treatment.
Argenx SE presents positive trial data for its treatment efgartigimod, showing significant improvement in patients with myositis and Sjogren’s disease.
Argenx SE presents positive trial data for its treatment efgartigimod, showing significant improvement in patients with myositis and Sjogren’s disease.