[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Pathos AI, Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":48},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100576464","phase-1-a-phase-1b2a-study-of-pocenbrodib-as-monotherapy-and-in-combination-with-darolutamide-in-participants-with-mcrpc-100576464",false,"NCT06785636","A Phase 1b\u002F2a Study of Pocenbrodib as Monotherapy and in Combination With Darolutamide in Participants With mCRPC","PATHWAY: A Phase 1b\u002F2a, Multicenter, Open- Label Study of Pocenbrodib as Monotherapy and in Combination With Darolutamide in Participants With Metastatic Castration-Resistant Prostate Cancer (mCRPC)","P300","1b \u002F 2a Inclusion Criteria:\n\n1. ≥18 years of age\n2. Histologic documentation of prostate adenocarcinoma\n3. Metastatic disease, documented by imaging. Imaging performed within 56 days prior to Screening is acceptable\n\n1b \u002F 2a Exclusion Criteria:\n\n1. Current or prior evidence of any small cell or neuroendocrine histology on the most recent prostate biopsy.\n2. Any liver metastases confirmed by biopsy or evidence of lesions \\>1 cm consistent with liver metastases on imaging.\n3. Intervention with any chemotherapy, investigational agent, or other anticancer drug, including enzalutamide, apalutamide, or darolutamide, 14 days prior to Cycle 1 Day 1 or 5 half-lives (whichever is shorter).\n4. Any other serious underlying medical, psychiatric, psychological, familial, or geographical condition, which in the judgment of the Investigator may interfere with study participation and compliance or place the participant at high risk from treatment-related complications.\n\n2a only -key inclusion criteria:\n\n1. Must have received at least 2 cycles of PLUVICTO®\n2. 1 line of prior any ARPI therapy\n3. No prior chemotherapy for mCRPC","MALE","18 Years",{"count":20,"type":21},120,"ESTIMATED","INTERVENTIONAL",[24,25],"PHASE1","PHASE2","This is a dose-finding study to assess the safety and preliminary antitumor activity of Pocenbrodib alone or with darolutamide in patients with metastatic castration-resistant prostate cancer (mCRPC)",[28,29],"mCRPC (Metastatic Castration-resistant Prostate Cancer)","Prostate Cancer",[31,32,33,34],"mCRPC, metastatic castrate resistant prostate cancer, prostate cancer,","darolutamide","Pocenbrodib","p300-CBP Transcription Factors","RECRUITING","2026-06-05",{"date":38,"type":39},"2026-06-10","ACTUAL",{"date":41,"type":39},"2025-02-07",{"date":43,"type":21},"2029-04-30",{"name":45,"class":46},"Pathos AI, Inc.","INDUSTRY",18,""]