Figure 1
Figure 1. Anti-CD79b ADCs with stable linkers regress tumors in multiple xenograft models. (A) The xenograft tumors of BJAB cells were allowed to grow to an average of 200 mm3 and then given a single dose intravenously of 50 μg or 16.6 μg of antibody-linked DM1 or MMAF/kg mouse. Unconjugated antibodies were dosed at 3.4 mg antibody/kg, equivalent to the highest amount of conjugated antibody. (B) Granta519 or (C) DoHH2 cell lines were treated as in panel A except that the drug doses were 100 μg or 33.3 μg conjugated DM1 or MMAF/kg mouse and the unconjugated antibody was dosed at 6.8 mg antibody/kg mouse. (D) The levels of surface CD79b expression on dissociated xenograft tumor cells and normal B cells as assayed by flow cytometry.

Anti-CD79b ADCs with stable linkers regress tumors in multiple xenograft models. (A) The xenograft tumors of BJAB cells were allowed to grow to an average of 200 mm3 and then given a single dose intravenously of 50 μg or 16.6 μg of antibody-linked DM1 or MMAF/kg mouse. Unconjugated antibodies were dosed at 3.4 mg antibody/kg, equivalent to the highest amount of conjugated antibody. (B) Granta519 or (C) DoHH2 cell lines were treated as in panel A except that the drug doses were 100 μg or 33.3 μg conjugated DM1 or MMAF/kg mouse and the unconjugated antibody was dosed at 6.8 mg antibody/kg mouse. (D) The levels of surface CD79b expression on dissociated xenograft tumor cells and normal B cells as assayed by flow cytometry.

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