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. 2021 May 27;26(9):e1514–e1525. doi: 10.1002/onco.13817
All Dose Levels, All Cycles
Name NC/NA 1 2 3 4 5 All grades
Fatigue 61% 22% 17% 0% 0% 0% 39%
Nausea 78% 11% 11% 0% 0% 0% 22%
Alanine aminotransferase increased 83% 6% 0% 11% 0% 0% 17%
Aspartate aminotransferase increased 83% 6% 0% 11% 0% 0% 17%
Diarrhea 83% 11% 6% 0% 0% 0% 17%
Dry mouth 83% 17% 0% 0% 0% 0% 17%
Abdominal pain 89% 0% 0% 11% 0% 0% 11%
Blood alkaline phosphatase increased 89% 0% 0% 11% 0% 0% 11%
Constipation 89% 6% 6% 0% 0% 0% 11%
Decreased appetite 89% 6% 6% 0% 0% 0% 11%
Hypokalemia 89% 11% 0% 0% 0% 0% 11%
Hypomagnesemia 89% 11% 0% 0% 0% 0% 11%
Hypophosphatemia 89% 6% 0% 6% 0% 0% 11%
Hypothyroidism 89% 0% 11% 0% 0% 0% 11%
Lymphopenia 83% 0% 0% 11% 6% 0% 17%
Musculoskeletal chest pain 89% 11% 0% 0% 0% 0% 11%
Musculoskeletal stiffness 89% 11% 0% 0% 0% 0% 11%
Pain in extremity 89% 11% 0% 0% 0% 0% 11%
Rash maculo‐papular 89% 11% 0% 0% 0% 0% 11%
Salivary hypersecretion 89% 6% 6% 0% 0% 0% 11%
Skin abrasion 89% 6% 6% 0% 0% 0% 11%
Vomiting 89% 11% 0% 0% 0% 0% 11%

Adverse Events Legend

Adverse events occurring in ≥10% of patients are shown.

There were no DLTs.

Abbreviation: NC/NA, no change from baseline/no adverse event.