This is a Phase 1/2, multicenter, open-label (unless otherwise specified in a combination-specific module) study of inlexisertib in combination with anticancer therapies. Modules within the master protocol are defined according to different combinations of inlexisertib with other anticancer agents.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Incidence of Adverse Events (Escalation Phase)
Timeframe: Approximately 24 months
Recommended Phase 2 Doses (RP2D) (Escalation Phase)
Timeframe: Approximately 18 months
Objective response rate (ORR) (Expansion Phase)
Timeframe: Approximately 24 months