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| AEs | N = 90 |
| AEs occurring during the study in ≥5% patients, n (%) | |
| Headache | 6 (7) |
| Nasopharyngitis | 6 (7) |
| Nausea | 5 (6) |
| Weight decrease | 5 (6) |
| Rash | 5 (6) |
| Study drug-related adverse events occurring in >1 patient | |
| Nausea | 3 (3) |
| Creatinine renal clearance decreased | 2 (2) |
| Serious adverse events | |
| HCC (not related to study drug) | 1 (1) |
AE, adverse event; HCC, hepatocellular carcinoma.
