Table 2.
Treatment-Related Adverse Events Reported in ≥10% of All Subjects
Adverse Event | Combination Treatment (SNX-5422 + Carboplatin/Paclitaxel) | ||||
All (N=23) | |||||
Any Grade n (%) | Grade 3/4 n (%) | ||||
Any | 22 (96) | 11 (48) | |||
Diarrhea | 16 (70) | 6 (26) | |||
Nausea | 11 (48) | 2 (9) | |||
Fatigue | 9 (39) | 0 | |||
Alopecia | 6 (26) | 0 | |||
Vomiting | 6 (26) | 1 (4) | |||
Thrombocytopenia | 4 (17) | 0 | |||
Neutropenia | 3 (13) | 2 (9) | |||
ALT increased | 3 (13) | 1 (4) | |||
ALP increased | 3 (13) | 0 | |||
Neuropathy* | 4 (17) | 1 (4) | |||
SNX-5422 Maintenance Monotherapy (N=13) | |||||
Grade 1 n (%) | Grade 2 n (%) | Grade 3 n (%) | Grade 4 n (%) | All Grade n (%) | |
Any | 1 (8) | 4 (31) | 2 (15) | 0 | 7 (54) |
Diarrhea | 0 | 1 (8) | 2 (15) | 0 | 3 (23) |
Nausea | 2 (15) | 0 | 0 | 0 | 2 (15) |
Fatigue | 1 (8) | 1 (8) | 0 | 0 | 2 (15) |
Decreased appetite | 1 (8) | 1 (8) | 0 | 0 | 2 (15) |
includes peripheral neuropathy and peripheral sensory neuropathy; one patient with adenocarcinoma was treated with SNX-5422 and included in the safety population, but was later found to not meet eligibility criteria and was withdrawn.