Vor Biopharma
VORPhase 3Vor Biopharma is pioneering a new approach to autoimmune disease by targeting the upstream drivers of B cell dysfunction with its lead asset, telitacicept. The company has a validated path forward, with telitacicept already approved and marketed for three indications in China and a broad global pipeline targeting over a million potential patients in the US alone. Led by an experienced team, Vor Bio is positioned to become a global leader in targeted autoimmune therapeutics, moving beyond symptom control to deliver durable, disease-modifying benefits.
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AI Company Overview
Vor Biopharma is pioneering a new approach to autoimmune disease by targeting the upstream drivers of B cell dysfunction with its lead asset, telitacicept. The company has a validated path forward, with telitacicept already approved and marketed for three indications in China and a broad global pipeline targeting over a million potential patients in the US alone. Led by an experienced team, Vor Bio is positioned to become a global leader in targeted autoimmune therapeutics, moving beyond symptom control to deliver durable, disease-modifying benefits.
Technology Platform
A TACI-Fc fusion protein platform designed for dual inhibition of the BAFF and APRIL cytokines, which are key upstream drivers of pathogenic B cell survival and autoantibody production in autoimmune diseases.
Pipeline Snapshot
66 drugs in pipeline, 4 in Phase 3
| Drug | Indication | Stage | Watch |
|---|---|---|---|
| Telitacicept + Placebo | Systemic Lupus Erythematosus | Phase 3 | |
| Telitacicept + Placebo | Generalized Myasthenia Gravis | Phase 3 | |
| Telitacicept + Placebo | Primary Sjogren's Disease | Phase 3 | |
| Telitacicept + Placebo | Systemic Lupus Erythematosus | Phase 3 | |
| VCAR33 | Leukemia, Myeloid, Acute | Phase 1/2 |
Funding History
4Total raised: $307M
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Competitive Landscape
Vor Bio competes with BAFF-only inhibitors like belimumab, CD20-depleting therapies, FcRn antagonists, and other B-cell modulators. Its key differentiation is the dual inhibition of BAFF and APRIL, which may offer superior efficacy in IgA-driven diseases and a validated clinical profile from its commercial experience in China.
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