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Adverse events (≥20% incidence) regardless of study drug relationship by preferred term (safety set) − overall (dose-escalation phase+follow-up phase)
| Preferred term | All patients, n (%) |
| Diarrhoea | 5 (50) |
| Nausea | 5 (50) |
| Fatigue | 3 (30) |
| Hyperglycaemia | 3 (30) |
| Hypophosphatemia | 3 (30) |
| Chills | 2 (20) |
| Tumour pain | 2 (20) |
| Weight decreased | 2 (20) |
