Table 2.
IC50 values of IBL-202 and venetoclax
IC50 | P* | ||
---|---|---|---|
Alone | In combination | ||
Primary CLL cells + CD40L fibroblasts | |||
IBL-202 | 0.47 ± 0.32 µM | 0.24 ± 0.03 µM | .01 |
Venetoclax | 30.2 ± 25.4 nM | 2.40 ± 0.30 nM | <.01 |
Primary CLL cells + HS-5 fibroblasts | |||
IBL-202 | 0.94 ± 0.24 µM | 0.53 ± 0.18 µM | <.01 |
Venetoclax | 36.37 ± 8.34 nM | 5.30 ± 1.80 nM | <.01 |
OSU-CLL cells | |||
IBL-202 | 0.61 ± 0.05 µM | 0.07 ± 0.01 µM | .01 |
Venetoclax | 295 ± 108 nM | 14.3 ± 1.20 nM | <.01 |
OSU-CLL-TP53ko cells | |||
IBL-202 | 1.89 ± 0.16 μM | 0.06 ± 0.01 µM | <.01 |
Venetoclax | 18.5 ± 2.26 μM | 0.63 ± 0.10 µM | .01 |
IC50 values for IBL-202 and venetoclax, alone and in combination, against primary CLL cells and OSU-CLL cell lines were calculated from the dose-response analyses.
P values shown indicate that in each of the culture conditions and in the 2 OSU-CLL lines, combining the drugs resulted in a significant decrease in the IC50 value for each drug compared with the IC50 values for the drugs as single agents. P values were calculated using the t test function of GraphPad Prism software.