Table 4.

Incidence of AEs (>15% of patients overall or >5% ≥grade 3)

AE category, SOC, PTAll patients (all duvelisib doses) (N = 210), n (%)
Grade Any 
Hematologic    
 Neutropenia 81 (38.6) 19 (9.0) 23 (11.0) 
 Anemia 52 (24.8) 29 (13.8) 1 (0.5) 
 Thrombocytopenia/decreased platelets 49 (23.3) 9 (4.3) 21 (10.0) 
Investigations    
 ALT increased 81 (38.6) 33 (15.7) 8 (3.8) 
 AST increased 79 (37.6) 30 (14.3) 2 (1.0) 
 Hypokalemia 31 (14.8) 5 (2.4) 6 (2.9) 
Nonhematologic    
 Diarrhea 88 (41.9) 24 (11.4) 
 Fatigue 85 (40.5) 17 (8.1) 1 (0.5) 
 Pyrexia 74 (35.2) 3 (1.4) 
 Nausea 67 (31.9) 7 (3.3) 
 Cough 66 (31.4) 1 (0.5) 
 Decreased appetite 44 (21.0) 2 (1.0) 
 Edema peripheral 43 (20.5) 1 (0.5) 
 Dyspnea 41 (19.5) 9 (4.3) 2 (1.0) 
 Headache 38 (18.1) 4 (1.9) 
 Vomiting 37 (17.6) 4 (1.9) 
 Arthralgia 35 (16.7) 4 (1.9) 
 Rash maculopapular 34 (16.2) 11 (5.2) 
 Upper respiratory tract infection 34 (16.2) 1 (0.5) 
 Rash 30 (14.3) 1 (0.5) 
 Constipation 32 (15.2) 1 (0.5) 
 Pneumonia 28 (13.3) 19 (9.0) 1 (0.5) 
AE category, SOC, PTAll patients (all duvelisib doses) (N = 210), n (%)
Grade Any 
Hematologic    
 Neutropenia 81 (38.6) 19 (9.0) 23 (11.0) 
 Anemia 52 (24.8) 29 (13.8) 1 (0.5) 
 Thrombocytopenia/decreased platelets 49 (23.3) 9 (4.3) 21 (10.0) 
Investigations    
 ALT increased 81 (38.6) 33 (15.7) 8 (3.8) 
 AST increased 79 (37.6) 30 (14.3) 2 (1.0) 
 Hypokalemia 31 (14.8) 5 (2.4) 6 (2.9) 
Nonhematologic    
 Diarrhea 88 (41.9) 24 (11.4) 
 Fatigue 85 (40.5) 17 (8.1) 1 (0.5) 
 Pyrexia 74 (35.2) 3 (1.4) 
 Nausea 67 (31.9) 7 (3.3) 
 Cough 66 (31.4) 1 (0.5) 
 Decreased appetite 44 (21.0) 2 (1.0) 
 Edema peripheral 43 (20.5) 1 (0.5) 
 Dyspnea 41 (19.5) 9 (4.3) 2 (1.0) 
 Headache 38 (18.1) 4 (1.9) 
 Vomiting 37 (17.6) 4 (1.9) 
 Arthralgia 35 (16.7) 4 (1.9) 
 Rash maculopapular 34 (16.2) 11 (5.2) 
 Upper respiratory tract infection 34 (16.2) 1 (0.5) 
 Rash 30 (14.3) 1 (0.5) 
 Constipation 32 (15.2) 1 (0.5) 
 Pneumonia 28 (13.3) 19 (9.0) 1 (0.5) 

AEs were coded using Medical Dictionary for Regulatory Activities, version 16.1, and were graded using the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.03.

PT, preferred term; SOC, system organ class.

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