Phase 1/2, open-label study of ETX-636 in participants with advanced solid tumors
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Evaluate Safety and Tolerability of ETX-636 monotherapy in Part A and ETX-636 plus fulvestrant combination therapy in Part B
Timeframe: First 28 days of treatment
Evaluate Safety and Tolerability of ETX-636 monotherapy in Part A and ETX-636 plus fulvestrant combination therapy in Part B
Timeframe: Average of 6 months
Select the Recommended Phase 2 Dose(s) (RP2D) in Part B to be further explored in Part C (combination therapy expansion)
Timeframe: Average of 6 months
Evaluate efficacy of ETX-636 plus fulvestrant combination therapy at the RP2D(s) in Part C
Timeframe: Average of 6 months