[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100639291":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":29,"centralContacts":38,"locations":44,"responsibleParty":62,"collaborators":29,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":29,"eligibilityCriteria":70,"healthyVolunteers":66,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":29,"studyType":77,"phases":78,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":85,"whyStopped":29,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":90,"completionDateStruct":92,"leadSponsor":94,"locationsCount":95},{"fullName":5,"class":6},"Akeso","INDUSTRY",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"AK138D1","EXPERIMENTAL","AK138D1 will be administered at pre-specified dose levels.",[13],"Drug: AK138D1",{"label":15,"type":10,"description":16,"interventionNames":17},"AK138D1+ Ivonescimab","AK138D1 and ivonescimab will be administered at pre-specified dose levels.",[13,18],"Drug: Ivonescimab",{"label":20,"type":10,"description":21,"interventionNames":22},"AK138D1 + Ivonescimab + Carboplatin","AK138D1, ivonescimab and carboplatin will be administered at pre-specified dose levels.",[13,18,23],"Drug: Carboplatin",[25,30,34],{"type":26,"name":9,"description":27,"armGroupLabels":28,"otherNames":29},"DRUG","Enrolled subjects will receive intravenous infusion (IV) of AK138D1 according to the dosing regimen specified in their cohort.",[9,20,15],null,{"type":26,"name":31,"description":32,"armGroupLabels":33,"otherNames":29},"Ivonescimab","Enrolled subjects will receive intravenous infusion (IV) of Ivonescimab according to the dosing regimen specified in their cohort.",[20,15],{"type":26,"name":35,"description":36,"armGroupLabels":37,"otherNames":29},"Carboplatin","Enrolled subjects will receive intravenous infusion (IV) of Carboplatin according to the dosing regimen specified in their cohort.",[20],[39],{"name":40,"role":41,"phone":42,"phoneExt":29,"email":43},"Xufang Yu","CONTACT","+86 (0760) 89873999","clinicaltrials@akesobio.com",[45],{"facility":46,"status":29,"city":47,"state":48,"zip":29,"country":49,"countryCode":50,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"Shanghai East Hospital","Shanghai","Shanghai Municipality","China","CN",{"type":52,"coordinates":53},"Point",[54,55],121.45806,31.22222,{"lat":55,"lon":54},[58],{"name":59,"role":41,"phone":60,"phoneExt":29,"email":61},"Caicun Zhou","+8613301825532","caicunzhoudr@163.com",{"type":63,"investigatorFullName":29,"investigatorTitle":29,"investigatorAffiliation":29,"oldNameTitle":29,"oldOrganization":29},"SPONSOR","100639291","phase-1-a-study-of-ak138d1-alone-or-in-combination-with-ivonescimab-in-advanced-non-small-cell-lung-cancer-100639291",false,"NCT07623356","A Study of AK138D1 Alone or in Combination With Ivonescimab in Advanced Non-Small Cell Lung Cancer","A Phase Ib\u002FII Study of AK138D1 as Monotherapy and in Combination With Ivonescimab in Patients With Advanced Non-Small Cell Lung Cancer","Inclusion Criteria:\n\n1. The subject must sign the written informed consent form (ICF) voluntarily;\n2. At enrollment, aged ≥ 18 to ≤ 75 years, both males and females are eligible;\n3. Has an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1;\n4. Has a life expectancy of ≥ 3 months;\n5. Has measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.\n6. Has Stage IIIB\u002FIIIC or IV NSCLC (American Joint Committee on Cancer \\[AJCC\\]).\n7. Adequate organ function.\n\nExclusion Criteria:\n\n1. Concomitant participation in another clinical study, unless it is a non-interventional clinical study or the follow-up period of an interventional study;\n2. Presence of active central nervous system (CNS) metastases.\n3. Live vaccines or attenuated live vaccines administered within 4 weeks prior to the first dose, or planned to be administered during the study; use of inactivated vaccines is allowed;\n4. Untreated subjects with active hepatitis B or active hepatitis C;\n5. Known active pulmonary tuberculosis (TB); subjects with suspected active TB must undergo appropriate clinical assessment to rule out the presence of active disease;\n6. Known active syphilis infection;\n7. Subjects with known allergy to any component of any study drug; and with a history of known severe hypersensitivity reactions to other monoclonal antibodies;\n8. Other reasons for ineligibility as evaluated by investigator.","ALL","18 Years","75 Years",{"count":75,"type":76},265,"ESTIMATED","INTERVENTIONAL",[79,80],"PHASE1","PHASE2","The goal of this clinical trial is to evaluate the safety, tolerability, and efficacy of AK138D1 as monotherapy or in combination with ivonescimab in patients with advanced non-small cell lung cancer.\n\nParticipants will receive study treatment with AK138D1 alone or in combination with ivonescimab, undergo safety assessments and tumor evaluations, and be followed for treatment tolerability, antitumor activity, and clinical outcomes.",[83],"Non-Small Cell Lung Cancer",[83],"NOT_YET_RECRUITING","2026-05-28",{"date":88,"type":89},"2026-06-03","ACTUAL",{"date":91,"type":76},"2026-06-18",{"date":93,"type":76},"2030-07-03",{"name":5,"class":6},1]