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Note: Tissue from a fresh pretreatment biopsy is preferred, however an archival sample is acceptable as long as the sample is no older than 5 years.\n* Received at least 1 and no more than 4 prior lines of systemic therapy following the initial diagnosis, after which single-agent therapy is considered an appropriate next therapeutic option.\n* Must have received bevacizumab unless there was a contraindication for its use.\n* If the tumor tests positive for FRα, participants must have received mirvetuximab soravtansine unless there is an exception for its use on medical grounds.\n\nExclusion Criteria:\n\n* Have endometrioid, clear cell, mucinous, or sarcomatous histology, mixed tumors containing any of these histologies, or low-grade\u002Fborderline ovarian cancer.\n* Have primary platinum-refractory disease: either did not respond (CR or PR) to first-line platinum-containing therapy or progressed on or within 3 months after the last dose of the first line platinum-containing therapy.\n* The tumor tests positive for FRα but the participant has not received mirvetuximab soravtansine for any reason other than medical contraindication.\n* Clinically significant or uncontrolled cardiac disease within 6 months before the first dose of study drug.\n* Known active CNS metastases and\u002For carcinomatous meningitis.\n* Known additional malignancy that is progressing or requires active treatment.\n\nOther protocol-defined Inclusion\u002FExclusion Criteria may apply.","FEMALE","18 Years","99 Years",{"count":808,"type":809},160,"ESTIMATED","INTERVENTIONAL",[812],"PHASE2","This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression.",[815],"Ovarian Cancer",[62],"2026-05-29",{"date":819,"type":820},"2026-06-01","ACTUAL",{"date":822,"type":820},"2025-11-12",{"date":824,"type":809},"2027-10-24",{"name":5,"class":6},79]