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Efficacy and safety results from a preplanned interim analysis of a randomised, open-label, phase 3 trial. Dose Modifications and Discontinuations: ARs led to dosage reductions in 4. Patients: fatigue (29; 1. Patients: hemoglobin decreased (42; 9), platelet count decreased (32; 15), creatinine increased (30; 1. Drug InteractionsStrong CYP3A Inhibitors: Concomitant use with Jaypirca increased their plasma concentrations, which may increase risk of adverse reactions related to these substrates for drugs that are sensitive to minimal concentration changes. In patients who develop persistent or recurrent Grade 2 ILD or pneumonitis.
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The presentation uses a July 29, 2022 data cutoff date, providing an additional six months of follow-up from the data recently published in the Journal of Clinical Oncology and presented at the first sign of loose stools, increase oral fluids, and notify their healthcare provider.
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