This study will assess the safety and efficacy of avutometinib (VS-6766) monotherapy and in combination with defactinib in subjects with recurrent Low-Grade Serous Ovarian Cancer (LGSOC)
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Part A: Determine optimal regimen of avutometinib (VS-6766) monotherapy or in combination with defactinib
Timeframe: From start of treatment to confirmation of response; 24 weeks
Part B: To determine the efficacy of the optimal regimen identified from Part A
Timeframe: From start of treatment to confirmation of response; 24 weeks
Part C: To evaluate additional efficacy parameters for the optimal regimen identified in Part A
Timeframe: From start of treatment to confirmation of response; 24 weeks
Part D:To evaluate additional efficacy parameters for a lower dose of avutometinib in combination with defactinib
Timeframe: From start of treatment to confirmation of response; 24 weeks