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1 humoral immune responses to the administered chimeric monoclonal antibody.
2 ntigens to two major subsets of DCs by using chimeric monoclonal antibodies.
4 ssed the safety and efficacy of siltuximab-a chimeric monoclonal antibody against interleukin 6-in HI
6 ese cells has been recently achieved using a chimeric monoclonal antibody against the pan B cell surf
7 rexate therapy with placebo or infliximab, a chimeric monoclonal antibody against TNF-alpha, in intra
9 in clinical trials include an immunotoxin, a chimeric monoclonal antibody, and an antibody drug conju
10 A phosphorylation site was introduced into chimeric monoclonal antibody B72.3 (MAb-chB72.3) by site
11 to tumor necrosis factor alpha, specifically chimeric monoclonal antibody cA2, in the treatment of Cr
17 ilability of c7E3 Fab (abciximab; ReoPro), a chimeric monoclonal antibody Fab fragment directed again
20 s directed against this receptor include the chimeric monoclonal antibody fragment abciximab, the pep
21 owing fusion of GDNF to the heavy chain of a chimeric monoclonal antibody (MAb) against the mouse tra
22 , where EPO is fused to the heavy chain of a chimeric monoclonal antibody (MAb) against the mouse tra
23 r the TNFR are fused to the heavy chain of a chimeric monoclonal antibody (MAb) against the mouse tra
24 has been developed wherein EPO is fused to a chimeric monoclonal antibody (MAb) against the mouse tra
25 rase IX (CAIX)-expressing tumor lesions with chimeric monoclonal antibody (mAb) girentuximab, which h
28 ccessful, compassionate use of the anti-CD20 chimeric monoclonal antibody rituximab in a patient with
34 ructed immunoglobulin G1 (IgG1) murine-human chimeric monoclonal antibody that binds the soluble subu
41 ted the efficacy and safety of infliximab, a chimeric monoclonal antibody to TNFalpha, in patients wi
43 pattern of opsonophagocytic activity of the chimeric monoclonal antibodies was similar to that of co
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