Obexelimab
Obexelimab, an investigational drug, is a bifunctional monoclonal antibody engineered to mimic the natural antigen-antibody complex for the inhibition of B cells. By targeting CD19 and FcγRIIb, obexelimab is designed to inhibit a broad B cell population, including plasmablasts and a subpopulation of CD19 expressing plasma cells, each of which produces high amounts of autoantibodies which contribute to autoimmune disease pathogenesis. Co-engagement of CD19 and FcγRIIb by obexelimab has been shown to inhibit B cell activity, including antibody production, proliferation, cytokine secretion, B cell differentiation and antigen presentation to T cells.
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Rapid recovery of B cells upon withdrawal of therapy
Preclinical and clinical data show that the return of B cells in circulation of patients receiving obexelimab was observed as soon as six weeks after discontinuation, compared with B cell recovery periods of six months or longer observed with anti-CD19 and anti-CD20 targeted depleting therapies.
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Enhanced disease management
Obexelimab’s self-administered, subcutaneous injection regimen could help patients to manage their own disease.
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Continuous versus intermittent B cell inhibition
Most B cell depleting agents are administered every six months by intravenous injection. Modest B cell recovery between doses can result in loss of efficacy. We believe obexelimab’s self-administered, subcutaneous injection regimen may ensure continuous suppression of B cell activity.
Our Pipeline
We are advancing two potential autoimmune disease franchise molecules, obexelimab and orelabrutinib, along with other pipeline and partnered programs for patients with autoimmune diseases. View our pipeline.
