Table 1.

Disposition of patients in the 7 subgroup-specific cohorts of the primary and extension studies

Enrolled in primary study (n = 79)Enrolled in extension study (n = 35) (%)Ongoing (n = 17) (%)
Idela + R 32 14 (44) 6 (19) 
 Idela 100 mg 3 (38) 3 (38) 
 Idela 150 mg 12 8 (67) 1 (8) 
 Delayed Idela 150 mg 12 3 (25) 2 (17) 
Idela + B 33 15 (45) 8 (24) 
 Idela 100 mg 1 (13) 1 (13) 
 Idela 150 mg 13 9 (69) 6 (46) 
 Delayed Idela 150 mg 12 5 (42) 1 (8) 
Idela + BR    
 Idela 150 mg 14 6 (43) 3 (21) 
Enrolled in primary study (n = 79)Enrolled in extension study (n = 35) (%)Ongoing (n = 17) (%)
Idela + R 32 14 (44) 6 (19) 
 Idela 100 mg 3 (38) 3 (38) 
 Idela 150 mg 12 8 (67) 1 (8) 
 Delayed Idela 150 mg 12 3 (25) 2 (17) 
Idela + B 33 15 (45) 8 (24) 
 Idela 100 mg 1 (13) 1 (13) 
 Idela 150 mg 13 9 (69) 6 (46) 
 Delayed Idela 150 mg 12 5 (42) 1 (8) 
Idela + BR    
 Idela 150 mg 14 6 (43) 3 (21) 

B, bendamustine; Idela, idelalisib; R, rituximab.

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