[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100602966":3},{"organization":4,"armGroups":7,"interventions":33,"overallOfficials":39,"centralContacts":43,"locations":49,"responsibleParty":69,"collaborators":39,"id":71,"slug":72,"hasResults":73,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":39,"eligibilityCriteria":77,"healthyVolunteers":73,"sex":78,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":39,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":39,"overallStatus":52,"whyStopped":39,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"Minghui Pharmaceutical (Hangzhou) Ltd","INDUSTRY",[8,15,18,21,24,27,30],{"label":9,"type":10,"description":11,"interventionNames":12},"Safety run-in phase: cohort 1","EXPERIMENTAL","Subjects will receive MHB036C Q3W in combination with MHB039A Q3W by intravenous administration.",[13,14],"Drug: MHB036C for Injection","Drug: MHB039A for Injection",{"label":16,"type":10,"description":11,"interventionNames":17},"Safety run-in phase: cohort 2",[13,14],{"label":19,"type":10,"description":11,"interventionNames":20},"Dose expansion phase: cohort 1",[13,14],{"label":22,"type":10,"description":11,"interventionNames":23},"Dose expansion phase: cohort 2",[13,14],{"label":25,"type":10,"description":11,"interventionNames":26},"Dose expansion phase: cohort 3",[13,14],{"label":28,"type":10,"description":11,"interventionNames":29},"Dose expansion phase: cohort 4",[13,14],{"label":31,"type":10,"description":11,"interventionNames":32},"Dose expansion phase: cohort 5",[13,14],[34,40],{"type":35,"name":36,"description":37,"armGroupLabels":38,"otherNames":39},"DRUG","MHB036C for Injection","Intravenous administration",[19,22,25,28,31,9,16],null,{"type":35,"name":41,"description":37,"armGroupLabels":42,"otherNames":39},"MHB039A for Injection",[19,22,25,28,31,9,16],[44],{"name":45,"role":46,"phone":47,"phoneExt":39,"email":48},"VP of R&D","CONTACT","+86 0571-869632","jwshi@minghuipharma.com",[50],{"facility":51,"status":52,"city":53,"state":54,"zip":55,"country":56,"countryCode":57,"cosmosGeoPoint":58,"geoPoint":63,"contacts":64},"Fudan University Shanghai Cancer Center","RECRUITING","Shanghai","Shanghai Municipality","201419","China","CN",{"type":59,"coordinates":60},"Point",[61,62],121.45806,31.22222,{"lat":62,"lon":61},[65],{"name":66,"role":46,"phone":67,"phoneExt":39,"email":68},"Ethics Committee","+86 021-64175590-85033","JJYIN555@163.com",{"type":70,"investigatorFullName":39,"investigatorTitle":39,"investigatorAffiliation":39,"oldNameTitle":39,"oldOrganization":39},"SPONSOR","100602966","phase-2-a-study-of-mhb036c-combined-with-mhb039a-in-patients-with-advanced-breast-cancer-or-other-advanced-malignant-solid-tumors-100602966",false,"NCT07130383","A Study of MHB036C Combined With MHB039A in Patients With Advanced Breast Cancer or Other Advanced Malignant Solid Tumors","An Open-label Phase II Clinical Study of MHB036C for Injection Combined With MHB039A for Injection in Patients With Advanced Breast Cancer or Other Advanced Malignant Solid Tumors","Inclusion Criteria:\n\n1. Voluntarily agrees to participate in the study and signs the informed consent form.\n2. Age ≥ 18 and ≤75 years, no restriction on gender.\n3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.\n4. Estimated life expectancy ≥ 3 months.\n5. Histologically or cytologically confirmed locally advanced or metastatic advanced solid tumors.\n6. At least one measurable lesion per RECIST v1.1 criteria.\n7. Adequate bone marrow reserve and organ function.\n8. Eligible participants of childbearing potential (males and females) must agree to take highly reliable contraceptive measures with their partners during the study and within at least 12 weeks after the last dose.\n\n   \\-\n\nExclusion Criteria:\n\n1. History of ≥2 primary malignancies within 5 years prior to informed consent.\n2. Received anti-tumor treatment within 4 weeks or within the 5 half-lives of the previous treatment (whichever is shorter) before dosing.\n3. Medication of other unmarketed investigational drugs or therapies within 4 weeks before dosing.\n4. Undergone major organ surgery (excluding biopsy) or significant trauma within 4 weeks before dosing or requiring elective surgery during the study.\n5. Vaccinated with attenuated live vaccines within 4 weeks before dosing.\n6. Treated with with systemic corticosteroids within 14 days before dosing.\n7. Central nervous system metastasis.\n8. Uncontrolled third-space effusion.\n9. Serious cardiovascular or cerebrovascular diseases.\n10. Severe lung disease affecting pulmonary function.\n11. Active infection requiring systemic therapy.\n12. Known hypersensitivity or delayed allergic reaction to the investigational product or its components.\n13. Drug abuse or other medical\u002Fpsychiatric condition that may interfere with study participation or results.\n14. Known alcohol or drug dependence.\n15. Pregnant or breastfeeding women, or individuals planning to conceive.","ALL","18 Years","75 Years",{"count":82,"type":83},210,"ESTIMATED","INTERVENTIONAL",[86],"PHASE2","This is an open-label, multicenter Phase II study of MHB036C combined with MHB039A in patients with advanced Breast Cancer or other advanced malignant solid tumors. The study was designed to evaluate the safety, tolerability, pharmacokinetics (PK), and efficacy of MHB036C and MHB039A combination therapy.",[89,90],"Advanced Breast Cancer","Advanced Malignant Solid Tumor","2025-11-16",{"date":93,"type":94},"2025-11-18","ACTUAL",{"date":96,"type":94},"2025-09-30",{"date":98,"type":83},"2031-08",{"name":5,"class":6},1]