[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100613692":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":32,"centralContacts":37,"locations":46,"responsibleParty":72,"collaborators":75,"id":79,"slug":80,"hasResults":81,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":81,"sex":87,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":31,"studyType":93,"phases":94,"briefSummary":96,"conditions":97,"keywords":100,"overallStatus":48,"whyStopped":31,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":105,"completionDateStruct":106,"leadSponsor":108,"locationsCount":109},{"fullName":5,"class":6},"Sun Yat-sen University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Experimental: Cohort A","EXPERIMENTAL","Experimental: Cohort A Intervention: Drug: WTX212A Monotherapy",[13],"Drug: WTX212A injection",{"label":15,"type":10,"description":16,"interventionNames":17},"Experimental: Cohort B","Experimental: Cohort B Intervention: Drug: WTX212A+Radiotherapy",[13,18],"Radiation: radiotherapy",[20,26],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","WTX212A injection","Erythrocyte-αPD-1 Antibody Conjugates",[9,15],[23],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"RADIATION","radiotherapy","Radiotherapy will be administered sequentially, with WTX212A treatment starting within one week after the completion of radiotherapy",[15],null,[33],{"name":34,"affiliation":35,"role":36},"RuiHua Xu, PhD","Cancer Center of SUN YAT-senU","PRINCIPAL_INVESTIGATOR",[38,42],{"name":34,"role":39,"phone":40,"phoneExt":31,"email":41},"CONTACT","020-87343468","xurh@sysucc.org.cn",{"name":43,"role":39,"phone":44,"phoneExt":31,"email":45},"Huiyan Luo, PhD","86-20-87343804","Luohy@sysucc.org.cn",[47,66],{"facility":35,"status":48,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"RECRUITING","Guangzhou","Guangdong","510000","China","CN",{"type":55,"coordinates":56},"Point",[57,58],113.25,23.11667,{"lat":58,"lon":57},[61,63,64],{"name":62,"role":39,"phone":40,"phoneExt":31,"email":41},"Ruihua Xu, PhD",{"name":62,"role":36,"phone":31,"phoneExt":31,"email":31},{"name":43,"role":65,"phone":31,"phoneExt":31,"email":31},"SUB_INVESTIGATOR",{"facility":67,"status":48,"city":49,"state":50,"zip":68,"country":52,"countryCode":53,"cosmosGeoPoint":69,"geoPoint":71,"contacts":31},"Cancer center of Sun Yat-sen University","510060",{"type":55,"coordinates":70},[57,58],{"lat":58,"lon":57},{"type":36,"investigatorFullName":73,"investigatorTitle":74,"investigatorAffiliation":5,"oldNameTitle":31,"oldOrganization":31},"Rui-hua Xu, MD, PhD","Principal Investigator",[76],{"name":77,"class":78},"Westlake Therapeutics","INDUSTRY","100613692","phase-1-a-phase-i-study-of-wtx212a-monotherapy-or-in-combination-with-radiotherapy-in-patients-with-advanced-solid-tumors-100613692",false,"NCT07269899","A Phase I Study of WTX212A Monotherapy or in Combination With Radiotherapy in Patients With Advanced Solid Tumors","A Phase I Study Evaluating the Preliminary Efficacy and Safety of WTX212A Injection as Monotherapy or in Combination With Radiotherapy in Patients With Advanced Solid Tumors","Reboot-107","Inclusion Criteria:\n\n1. Voluntarily signed informed consent, understanding of the study, and willingness and ability to complete all study procedures.\n2. Male or female, aged 18 to 75 years (inclusive).\n3. Patients with histologically and\u002For cytologically confirmed advanced malignant tumors.\n\nExclusion Criteria:\n\n1. Suffering from other serious internal diseases, including but not limited to: uncontrolled diabetes, active peptic ulcer, liver cirrhosis, active bleeding, etc., those with uncontrollable or severe cardiovascular diseases, such as NYHA Class II or higher congestive heart failure, unstable angina, myocardial infarction, etc., within 6 months before the first dose, difficult to control hypertension (systolic blood pressure ≥180mmHg and\u002For diastolic blood pressure ≥100mmHg).\n2. Uncontrollable pleural effusion, peritoneal effusion, or pericardial effusion requiring puncture and drainage, or recurrence requiring re-drainage after puncture and drainage.\n3. History of pulmonary fibrosis, interstitial pneumonia, pneumoconiosis, radiation pneumonitis, drug-related pneumonia, or severe lung function impairment.\n4. Previous IO drug treatment with adverse events related to the drug that required permanent discontinuation of IO treatment.","ALL","18 Years","75 Years",{"count":91,"type":92},12,"ESTIMATED","INTERVENTIONAL",[95],"PHASE1","This is a single-arm, open-label, investigator-initiated clinical study (IIT) designed to evaluate the preliminary efficacy, safety, tolerability, immunogenicity, and pharmacokinetic (PK) characteristics of WTX212A Injection in patients with advanced solid tumors.",[98,99],"Solid Tumor Cancer","Cancer",[98,99],"2025-11-25",{"date":103,"type":104},"2025-12-08","ACTUAL",{"date":101,"type":104},{"date":107,"type":92},"2027-08-30",{"name":5,"class":6},2]