Stopped: The decision of early termination was made due to business reasons, and was not based on any safety concerns for any of the treatment combinations.
A phase Ib, open-label platform study of select drug combinations chosen in order to characterize safety and tolerability of each treatment arm tested and to identify recommended doses and regimens for future studies.
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Incidence and nature of dose limiting toxicities (DLTs) in the first cycle
Timeframe: 30 months
Incidence and severity of AEs and SAEs, including changes in laboratory values, vital signs, and ECGs
Timeframe: 34 months
Frequency of dose interruptions
Timeframe: 30 months
Frequency of dose reductions
Timeframe: 30 months
Dose intensity
Timeframe: 30 months