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. 2009 Aug;157(2):198–208. doi: 10.1111/j.1365-2249.2009.03979.x

Table 2.

Investigational B cell-directed biological therapies for treating autoimmune disorders.

Diseases
Agent Pharmaceutical company Target Form Phases I/II Phase III
Anti-CD20 therapies
Ocrelizumab Genentech/Roche/Biogen-Idec CD20 Humanized mAb RA MS (RR) RA RA SLE (lupus nephritis)
Ofatumumab GSK/Genmab CD20 Human mAb RA MS RA
Veltuzumab Nycomed/Immunomedics CD20 Humanized mAb ITP
SBI-087 Tru-015 Wyeth/Trubion CD20 SMIP RA SLE
Anti-CD22 therapies
Epratuzumab UCB/Immunomedics CD22 Humanized mAb SLE
Anti-CD19 therapies
MDX-1342 Medarex CD19 Human mAb RA
BAFF and APRIL Blockers
Belimumab GSK/Human Genome Sciences BlyS (BAFF) Human mAb RA SLE
Atacicept EMD Serono BAFF April TACI-Ig receptor RAa MS SLE
A-623 Anthera Pharmaceuticals BAFF Peptide fusion protein SLE
CD40 – CD40L blockers
Ruplizumab (hu5c8; BG9588) Biogen-IDEC CD40L (CD154) Humanized mAb SLE ITP terminated (thrombotic events)
Toralizumab (IDEC-131) Biogen-IDEC CD40L (CD154) Humanized mAb SLE ITP terminated (thrombotic events)
a

Alone and in combination after rituximab therapy. ITP, immune thrombocytopenic purpura; SLE, systemic lupus erythematosus; MS, multiple sclerosis; MS (RR), MS relapsing–remitting; RA, rheumatoid arthritis; mAb, monoclonal antibody; BAFF, B cell activating factor belonging to the TNF family.