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1 d CD20, the target for antibody therapy with Rituxan.
2 mab (chimeric anti-CD20 monoclonal antibody, Rituxan), alone or in conjunction with chemotherapy, has
3 own to activate complement (e.g., Herceptin, Rituxan, and Erbitux) could be significantly enhanced if
4 ort demonstrating the safety and efficacy of Rituxan anti-CD20 chimeric antibody in combination with
6 o demonstrate the safety and efficacy of the Rituxan chimeric anti-CD20 antibody in combination with
8 get the cell surface marker CD20 (rituximab; Rituxan for hematologic malignancies and rheumatoid arth
13 The chimeric anti-CD20 antibody rituximab (Rituxan, IDEC-C2B8) is widely used in the clinical treat
14 tuximab (chimeric mouse anti-human CD20 mAb, Rituxan, IDEC-C2B8), alone and/or combined with chemothe
16 therapy with monoclonal antibody rituximab (Rituxan) in a short period of time and continued to be t
22 dex (IPI) score > or = 2, the combination of Rituxan plus CHOP achieved an ORR of 89% and CR of 56%.
23 d the monoclonal antibody to CD20 rituximab (Rituxan) promoted long-term islet allograft survival in
24 ts trastuzumab (Herceptin(R)) and rituximab (Rituxan(R)), engaged both activation (FcgammaRIII) and i
25 ecific CTLs can eradicate both untreated and Rituxan-resistant lymphomatous EBV-LPD, with failures as
27 himeric anti-CD20 monoclonal antibody (mAb) (Rituxan) was approved for the treatment of low-grade/fol
29 f IgG or F(ab')(2) homodimers vs monomers of Rituxan were compared for their ability to inhibit the g
31 e most frequent adverse events attributed to Rituxan were fever and chills, primarily during the firs
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