Safety results showed that treatment-related, treatment-emergent adverse events (TEAEs) of grade 3 or higher reported in 68.8% of patients (n = 22), and the most commonly reported toxicities included neutropenia (31.3%), febrile neutropenia (12.5%), and hypokalemia (12.5%). Notably, no patients in the pooled population who received a 50 mg/m2 and 60 mg/m2 dose of the regimen experienced treatment-related grade 3 or higher peripheral neuropathy or fatigue. Read more . . .