Stopped: Funding source withdrew financial support prior to start of Phase II portion of study
This is an open label nonrandomized Phase I/ IIA trial designed to assess the safety, tolerability, and efficacy of apatinib in combination with pembrolizumab. Phase I will assess the safety of combining increasing oral daily doses of apatinib with a fixed dose of IV pembrolizumab every three weeks and will determine the RP2D (Recommended Phase 2 Dose). Phase II will assess the efficacy of the RP2D of apatinib in combination with pembrolizumab and provide additional safety and tolerability data in three disease-specific cohorts
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Incidence of dose limiting toxicities (DLTs) of Apatinib in combination with pembrolizumab
Timeframe: 21 days, one cycle
Objective Response Rate (ORR) (Phase II)
Timeframe: 12 months