[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"United Immunity, co., Ltd.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":43},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100639508",false,"NCT07605962","Phase 1\u002F2 Study of UI-102 in Selected Advanced Cancers","A Phase I\u002FII Open-Label, Dose Escalation, Dose Optimization, and Cohort Expansion Trial to Investigate the Safety, Pharmacokinetics and Pharmacodynamics of UI-102, a Novel Cholesteryl Pullulan (CHP) Nanoparticle-formulated TLR7\u002F8 Agonist in Patients With Selected Locally Advanced and\u002For Metastatic Solid Tumors","Inclusion Criteria:\n\n* Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1,\n* 18 Years and Older (adult, older adult),\n* Histologically confirmed advanced cancer,\n* Archived or fresh tumor tissue sample that must be confirmed as adequate,\n* Evaluable\u002FMeasurable disease per RECIST 1.1,\n* Previously received applicable standard treatments,\n* Male and female participants of childbearing potential who are sexually active with a non-sterilized partner must agree to use highly effective methods of birth control\n\nExclusion Criteria:\n\n* central nervous system metastasis,\n* Ongoing or uncontrolled ascites or pleural effusion,\n* Significant ongoing toxicity from prior anticancer treatment,\n* Out-of-range laboratory values,\n* Clinically significant lung, heart, or autoimmune disease,\n* Ongoing requirement for immunosuppressive treatment,\n* Significant secondary malignancy,\n* Hypersensitivity to study drug or excipients,\n* Pregnant or lactating,\n* Ongoing active infection","ALL","18 Years",{"count":18,"type":19},140,"ESTIMATED","INTERVENTIONAL",[22,23],"PHASE1","PHASE2","This phase 1\u002F2 first-in-human study is designed to assess the safety and efficacy of UI-102, a TLR7\u002F8 agonist encapsulated in a Cholesteryl Pullulan Nanoparticle.",[26],"Advanced Cancer",[28,29],"metastatic solid tumors","advanced solid tumors","RECRUITING","2026-06-01",{"date":33,"type":34},"2026-06-03","ACTUAL",{"date":36,"type":34},"2026-05-20",{"date":38,"type":19},"2031-03-31",{"name":40,"class":41},"United Immunity, co., Ltd.","INDUSTRY",3,""]