[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100565485":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":29,"centralContacts":33,"locations":38,"responsibleParty":54,"collaborators":24,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":24,"eligibilityCriteria":62,"healthyVolunteers":58,"sex":63,"minAge":64,"maxAge":24,"enrollmentInfo":65,"targetDuration":24,"studyType":68,"phases":69,"briefSummary":72,"conditions":73,"keywords":24,"overallStatus":41,"whyStopped":24,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},{"fullName":5,"class":6},"Akeso","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"AK129","EXPERIMENTAL","Phase Ia: Subjects will receive AK129: different doses on every 2 weeks.",[13],"Drug: AK129",{"label":15,"type":10,"description":16,"interventionNames":17},"AK129+AK117","Phase Ib: Subjects will receive: AK129: different doses on every 2 weeks, AK117: 30mg\u002Fkg on every 2 weeks.\n\nPhase II: Subjects will receive: AK129: recommended phase II dose (RP2D) from phase Ib on every 2 weeks, AK117: 30mg\u002Fkg on every 2 weeks.",[13,18],"Drug: AK117",[20,25],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":24},"DRUG","Subjects receive AK129 intravenously.",[9,15],null,{"type":21,"name":26,"description":27,"armGroupLabels":28,"otherNames":24},"AK117","Subjects receive AK117 intravenously.",[15],[30],{"name":31,"affiliation":5,"role":32},"Wenting Li, MD","STUDY_DIRECTOR",[34],{"name":31,"role":35,"phone":36,"phoneExt":24,"email":37},"CONTACT","+86(0760)89873999","clinicaltrials@akesobio.com",[39],{"facility":40,"status":41,"city":42,"state":24,"zip":24,"country":43,"countryCode":44,"cosmosGeoPoint":45,"geoPoint":50,"contacts":51},"Beijing Cancer Hospital","RECRUITING","Beijing","China","CN",{"type":46,"coordinates":47},"Point",[48,49],116.39723,39.9075,{"lat":49,"lon":48},[52],{"name":53,"role":35,"phone":24,"phoneExt":24,"email":24},"Yuqin Song",{"type":55,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR","100565485","phase-1-a-study-of-ak129-with-or-without-ak117-in-pdl1-refractory-classic-hodgkin-lymphoma-100565485",false,"NCT06642792","A Study of AK129 With or Without AK117 in PD(L)1-refractory Classic Hodgkin Lymphoma","A Phase I\u002FII Study of AK129 (Bispecific Antibody Targeting LAG-3 and PD-1) Monotherapy or in Combination With AK117 (Anti-CD47 Monoclonal Antibody) in Relapse or Refractory Classic Hodgkin Lymphoma With PD-1\u002FL1 Inhibitor Treatment Failure","Inclusion Criteria:\n\n* Age ≥ 18 years old at the time of enrolment.\n* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.\n* Expected Survival of ≥ 12 weeks.\n* Diagnosed as R\u002FR cHL according to Lugano 2014 criteria.\n* Has progressed on treatment with PD-1\u002FL1 inhibitior therapy.\n* Has adequate organ function.\n* All female and male subjects of reproductive potential must agree to use an effective method of contraception from the start of screening until 120 days after the last dose of study treatment.\n\nExclusion Criteria:\n\n* Diagnosed with nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL) or gray zone lymphoma.\n* Central nervous system (CNS) lymphoma involvement.\n* Known history of human T-cell leukemia virus type 1 (HTLV-1) infection.\n* Autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T cell immunotherapy (CAR-T) within 90 days prior to the first dose of study treatment.\n* Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation (allo-HSCT).\n* Previous use of any agents targeting the CD47-SIRPα pathway, LAG-3 pathway, or similar targets.\n* Has other malignancies within 3 years prior to the first dose or residual lesions from other malignancies diagnosed more than 3 years ago.\n* Has an active autoimmune disease requiring systemic treatment within 2 years prior to the first dose.\n* History of active or previously confirmed inflammatory bowel disease.\n* History of interstitial lung disease requiring corticosteroid therapy, or current interstitial lung disease.\n* Has known active Hepatitis B or Hepatitis C.\n* Unresolved toxicity from previous anti-tumor treatment.\n* Uncontrolled comorbidities.","ALL","18 Years",{"count":66,"type":67},280,"ESTIMATED","INTERVENTIONAL",[70,71],"PHASE1","PHASE2","This is a phase I\u002FII study. All subjects are patients diagnosed with relapse or refractory (R\u002FR) classic Hodgkin lymphoma (cHL) and has progressed on treatment with PD-1\u002FL1 inhibitor therapy. The purpose of this study is to evaluate the safety and efficacy of AK129 (bispecific antibody targeting LAG-3 and PD-1) monotherapy or in combination with AK117 (anti-CD47 monoclonal antibody) in R\u002FR cHL with PD-1\u002FL1 inhibitor treatment failure.",[74],"Classic Hodgkin Lymphoma","2025-02-09",{"date":77,"type":78},"2025-02-11","ACTUAL",{"date":80,"type":78},"2025-01-17",{"date":82,"type":67},"2028-02",{"name":5,"class":6},1]