[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100485932":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":24,"centralContacts":25,"locations":35,"responsibleParty":160,"collaborators":24,"id":162,"slug":163,"hasResults":164,"nctId":165,"briefTitle":166,"officialTitle":167,"acronym":24,"eligibilityCriteria":168,"healthyVolunteers":164,"sex":169,"minAge":170,"maxAge":24,"enrollmentInfo":171,"targetDuration":24,"studyType":174,"phases":175,"briefSummary":177,"conditions":178,"keywords":181,"overallStatus":38,"whyStopped":24,"lastUpdateSubmitDate":187,"lastUpdatePostDateStruct":188,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":195,"locationsCount":196},{"fullName":5,"class":6},"EpimAb Biotherapeutics (Suzhou)Co., Ltd.","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"EMB-07-Patients with solid tumor","EXPERIMENTAL","Patients with solid tumor will receive intravenous infusions of EMB-07 weekly (QW). Dose escalation will continue until the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) is reached or all planned doses are administered.",[13],"Drug: EMB07",{"label":15,"type":10,"description":16,"interventionNames":17},"EMB07-Patients with lymphoma","Patients with lymphoma will receive intravenous infusions of EMB-07 weekly (QW). Dose escalation will continue until the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) is reached or all planned doses are administered.",[13],[19],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":24},"DRUG","EMB07","EMB07 is a MAT-Fab bispecific antibody against CD3 and RORI",[9,15],null,[26,31],{"name":27,"role":28,"phone":29,"phoneExt":24,"email":30},"Sai Lou","CONTACT","+8613758235260","slou@epimab.com",{"name":32,"role":28,"phone":33,"phoneExt":24,"email":34},"Junqiang He","+8618302157016","jqhe@epimab.com",[36,53,65,79,90,101,114,125,136,149],{"facility":37,"status":38,"city":39,"state":40,"zip":24,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Peninsula and South Eastern Haematology and Oncology Group","RECRUITING","Frankston","Victoria","Australia","AU",{"type":44,"coordinates":45},"Point",[46,47],145.12291,-38.14458,{"lat":47,"lon":46},[50],{"name":51,"role":52,"phone":24,"phoneExt":24,"email":24},"Ganju","PRINCIPAL_INVESTIGATOR",{"facility":54,"status":38,"city":55,"state":56,"zip":24,"country":41,"countryCode":42,"cosmosGeoPoint":57,"geoPoint":61,"contacts":62},"One Clinical Research","Nedlands","Western Australia",{"type":44,"coordinates":58},[59,60],115.8073,-31.98184,{"lat":60,"lon":59},[63],{"name":64,"role":52,"phone":24,"phoneExt":24,"email":24},"Ariyapperuma",{"facility":66,"status":38,"city":67,"state":68,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":71,"geoPoint":75,"contacts":76},"Hunan Cancer Hospital","Changsha","Hunan","China","CN",{"type":44,"coordinates":72},[73,74],112.97087,28.19874,{"lat":74,"lon":73},[77],{"name":78,"role":28,"phone":24,"phoneExt":24,"email":24},"Quchang Ouyang",{"facility":80,"status":38,"city":81,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":82,"geoPoint":86,"contacts":87},"Affiliated Hospital of Hebei University","Baoding",{"type":44,"coordinates":83},[84,85],115.46246,38.87288,{"lat":85,"lon":84},[88],{"name":89,"role":28,"phone":24,"phoneExt":24,"email":24},"Youchao Jia",{"facility":91,"status":38,"city":92,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":93,"geoPoint":97,"contacts":98},"Cancer Hospital Chinese Academy of Medical Sciences","Beijing",{"type":44,"coordinates":94},[95,96],116.39723,39.9075,{"lat":96,"lon":95},[99],{"name":100,"role":52,"phone":24,"phoneExt":24,"email":24},"Yuankai Shi",{"facility":102,"status":38,"city":103,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":104,"geoPoint":108,"contacts":109},"The First Affiliated Hospital of Bengbu Medical College","Bengbu",{"type":44,"coordinates":105},[106,107],117.36083,32.94083,{"lat":107,"lon":106},[110,112],{"name":111,"role":28,"phone":24,"phoneExt":24,"email":24},"Yanli Yang",{"name":113,"role":28,"phone":24,"phoneExt":24,"email":24},"Huan Zhou",{"facility":115,"status":38,"city":116,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":117,"geoPoint":121,"contacts":122},"Zhujiang Hospital of Southern Medical University","Guangzhou",{"type":44,"coordinates":118},[119,120],113.25,23.11667,{"lat":120,"lon":119},[123],{"name":124,"role":28,"phone":24,"phoneExt":24,"email":24},"Sanfang Tu",{"facility":126,"status":38,"city":127,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":128,"geoPoint":132,"contacts":133},"The Affiliated Tumour Hospital of Harbin Medical University","Harbin",{"type":44,"coordinates":129},[130,131],126.65,45.75,{"lat":131,"lon":130},[134],{"name":135,"role":28,"phone":24,"phoneExt":24,"email":24},"Qingyuan Zhang",{"facility":137,"status":38,"city":138,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":139,"geoPoint":143,"contacts":144},"Shandong Cancer Hospital","Shandong",{"type":44,"coordinates":140},[141,142],120.48412,40.28464,{"lat":142,"lon":141},[145,147],{"name":146,"role":28,"phone":24,"phoneExt":24,"email":24},"Zengjun Li",{"name":148,"role":28,"phone":24,"phoneExt":24,"email":24},"Yuping Sun",{"facility":150,"status":38,"city":151,"state":24,"zip":24,"country":69,"countryCode":70,"cosmosGeoPoint":152,"geoPoint":156,"contacts":157},"Tianjin Medical University Cancer Institue & Hospital","Tianjin",{"type":44,"coordinates":153},[154,155],117.17667,39.14222,{"lat":155,"lon":154},[158],{"name":159,"role":28,"phone":24,"phoneExt":24,"email":24},"Lanfang Li",{"type":161,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR","100485932","phase-1-first-in-human-study-of-emb-07-in-locally-advancedmetastatic-solid-tumors-or-relapserefractory-lymphoma-100485932",false,"NCT05607498","First in Human Study of EMB-07 in Locally Advanced\u002FMetastatic Solid Tumors or Relapse\u002FRefractory Lymphoma","A First-in-human, Phase I, Open-Label Study of EMB-07, a Bi-specific Antibody Anti-CD3 and Receptor Tyrosine Kinase-like Orphan Receptor 1 (ROR1) in Patients With Locally Advanced\u002FMetastatic Solid Tumors or Relapse\u002FRefractory Lymphoma","Inclusion Criteria:\n\n1. Willing and able to provide signed and dated informed consent prior to any study-related procedures and willing and able to comply with all study procedures.\n2. Male or female, and aged ≥ 18 years\n3. Treatment group A: Patients with histologically or cytologically locally advanced unresectable or metastatic solid tumors limiting to triple-negative breast cancer, lung adenocarcinoma, ovarian cancer, pancreatic cancer, colorectal cancer, gastric cancer, prostate cancer, bladder cancer, and uterus cancer. Treatment group B: Patients with histologically or cytologically relapse\u002Frefractory lymphoma limiting to chronic lymphocytic leukemia\u002Fsmall lymphocytic lymphoma (CLL\u002FSLL), mantle cell lymphoma (MCL) and diffuse large B cell lymphoma (DLBCL).\n4. Treatment group A: Standard therapies do not exist, or are no longer effective, or are not tolerable or accessible to the patient measurable or evaluable disease per RECIST V1.1. Treatment group B: Presence of at least one two-dimensional measurable lesion confirmed by imaging (CT or MRI) (either lymph nodes lesions with any long diameter \\> 1.5 cm or extranodal lesions with any long diameter \\> 1.0 cm); for CLL patients whose baseline imaging evaluation determined that no two-dimensional measurable lesions, their peripheral blood monoclonal B lymphocytes should be ≥ 5.0×109\u002FL.\n5. Patients must provide archival tumor samples, or a biopsy will be required if archival tumor sample is not available. Archival tumor sample must be taken ≤ 2 years prior to screening, otherwise a fresh tumor biopsy at screening is required.\n6. ECOG performance status 0 or 1\n7. Adequate organ function to participate in the trial.\n8. Recovery from adverse events (AEs) related to prior anticancer therapy.\n\nExclusion Criteria:\n\n1. Prior treatment with any agent targeting ROR1.\n2. History of Grade 4 immune-related adverse events (irAEs) or irAEs requiring discontinuation of prior therapies.\n3. Patient with primary central nervous system (CNS) malignancy or symptomatic CNS metastases. Patients with solid tumors with CNS metastases are eligible if they do not need to receive local radiation treatment at the discretion of investigator or if radiation therapy for CNS metastases is completed ≥ 4 weeks prior to study treatment.\n4. Anticancer therapy or radiation \\\u003C 5 half-lives or 4 weeks (whichever is shorter) prior to study treatment.\n5. Abuse on alcohol, cannabis-derived products, or other drugs.","ALL","18 Years",{"count":172,"type":173},150,"ESTIMATED","INTERVENTIONAL",[176],"PHASE1","For solid tumors and lymphoma, respectively: This study is to evaluate the safety and tolerability of EMB-07 and to determine the maximum tolerated dose (MTD) and\u002For recommended Phase 2 dose (RP2D). Pharmacokinetics (PK), immunogenicity, and the anti-multiple myeloma activity of EMB-07 will also be assessed.",[179,180],"Advanced\u002FMetastatic Solid Tumors","Relapse\u002FRefractory Lymphoma",[182,183,184,185,21,186,179,180],"Phase I","Bispecific antibody","CD3","ROR1","Dose escalation","2025-02-28",{"date":189,"type":190},"2025-03-03","ACTUAL",{"date":192,"type":190},"2023-03-01",{"date":194,"type":173},"2026-03-31",{"name":5,"class":6},10]