Immunovant
IMVTPhase 3Immunovant is dedicated to enabling normal lives for people with autoimmune diseases by developing targeted anti-FcRn therapies. The company's lead assets, batoclimab and IMVT-1402, are in clinical development for a range of IgG-mediated conditions, with positive Phase 2b results recently announced for batoclimab. As a subsidiary of Roivant Sciences, Immunovant leverages a patient-focused, innovative approach to address complex autoimmune disease needs.
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AI Company Overview
Immunovant is dedicated to enabling normal lives for people with autoimmune diseases by developing targeted anti-FcRn therapies. The company's lead assets, batoclimab and IMVT-1402, are in clinical development for a range of IgG-mediated conditions, with positive Phase 2b results recently announced for batoclimab. As a subsidiary of Roivant Sciences, Immunovant leverages a patient-focused, innovative approach to address complex autoimmune disease needs.
Technology Platform
Platform of anti-neonatal Fc receptor (anti-FcRn) monoclonal antibodies designed to inhibit IgG recycling, promoting the degradation of pathogenic immunoglobulin G (IgG) autoantibodies that drive autoimmune diseases.
Pipeline Snapshot
1919 drugs in pipeline, 5 in Phase 3
| Drug | Indication | Stage |
|---|---|---|
| Batoclimab + Placebo | Thyroid Eye Disease | Phase 3 |
| Batoclimab | Thyroid Eye Disease | Phase 3 |
| Batoclimab 680 mg SC weekly + Batoclimab 340 mg SC weekly + Matching Placebo SC ... | Generalized Myasthenia Gravis | Phase 3 |
| IMVT-1402 + IMVT-1402 + Placebo + IMVT-1402 | Generalized Myasthenia Gravis | Phase 3 |
| Batoclimab + Placebo | Thyroid Eye Disease | Phase 3 |
Funding History
3Total raised: $625M
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Risk Factors
Competitive Landscape
Immunovant competes in the anti-FcRn space against approved therapies like Argenx's Vyvgart and UCB's rozanolixizumab, as well as late-stage candidates from large pharma like Johnson & Johnson's nipocalimab. Its differentiation strategy focuses on tailored dosing and developing next-generation candidates with potentially improved tolerability profiles.
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