[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"FBD Biologics Limited\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":74},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100553556","phase-1-an-engineered-sirp-fused-to-anti-pd-l1-and-tgf--fusion-protein-hcb301-in-subjects-with-selected-advanced-tumors-100553556",false,"NCT06487624","An Engineered Sirpα Fused to Anti-Pd-L1 And Tgf-β Fusion Protein (HCB301) in Subjects With Selected Advanced Tumors","A Phase 1, Open-label, Multicenter, Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of HCB301 in Subjects With Advanced Solid Tumors or Relapsed and Refractory cHL","Inclusion Criteria:\n\n1. Able to understand and be willing to sign the ICF.\n2. Male and female subjects of ≥18 years of age.\n3. Histologically\u002Fcytologically confirmed, locally advanced solid tumor:\n\n   subjects confirmed advanced solid tumors who have relapsed or refractory and should have no options for standard or approved therapies known to potentially confer clinical benefit or classical Hodgkin lymphoma, relapsed or refractory to at least 2 prior lines of systemic therapy.\n4. For subjects with advanced solid tumors - must have at least 1 measurable lesion as defined by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 at baseline.\n5. For subjects with classical Hodgkin lymphoma - must have classical Hodgkin lymphoma that is measurable or assessable for response.\n6. Must have ECOG performance status of 0 to 1 at Screening.\n7. Able to provide tumor tissue samples.\n8. Have a life expectancy of ≥12 weeks.\n\nExclusion Criteria:\n\n1. With known history of hypersensitivity to any components of HCB301.\n2. Known active or untreated CNS metastases and\u002For carcinomatous meningitis.\n3. Have undergone a major surgery or radical radiotherapy within 28 days or palliative radiotherapy within 14 days or have used a radioactive drug within 56 days prior to the first dose of HCB301.\n4. Clinically significant cardiovascular condition.\n5. Any previous treatment-related toxicities which have not recovered to ≤ Grade 1 as evaluated by National Cancer Institute, Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0 or baseline, except alopecia and anemia.\n6. With known inherited or acquired bleeding disorder or bleeding diathesis. .\n7. Have RBC transfusion within 4 weeks prior to Screening.\n8. With a previously documented diagnosis of hemolytic anemia or Evans Syndrome in the last 3 months.\n9. Any investigational or approved systemic cancer therapy administered within 21 days or 5 half-lives, whichever is shorter, before the first dose of the study drug.\n10. Active use of vitamin K antagonist anticoagulant like warfarin. Use of low molecular weight heparin and factor Xa inhibitors will be permitted on case by case basis. There will be no restriction for daily aspirin ≤ 100 mg\u002FQD.\n11. Have used herbal medication within 14 days prior to the first dose of HCB301.\n12. Have received any treatment targeting the SIRPα-CD47, PD-L1, or TGF-β pathway.\n13. Have other malignancies requiring treatment within 2 years prior to the first dose of HCB301.\n14. An investigational device used within 28 days prior to the first dose of HCB301.\n15. Positive for hepatitis B, active hepatitis C infections, positive for HIV, or known active or latent tuberculosis.\n16. Known to have a history of alcoholism or drug abuse.","ALL","18 Years",{"count":19,"type":20},50,"ESTIMATED","INTERVENTIONAL",[23],"PHASE1","The purpose of this study is to find out whether IV injection of HCB301 is an effective treatment for different types of advanced solid tumors and relapsed and refractory classical Hodgkin lymphomas and what side effects (unwanted effects) may occur in subjects aged 18 years old and above.",[26,27],"Advanced Solid Tumor","Refractory Hodgkin Lymphoma",[29,30,31,32,33,34],"Immunotherapy","CD47","PD-L1","TGF-beta","Tumor","Cancer","RECRUITING","2026-04-07",{"date":38,"type":39},"2026-04-13","ACTUAL",{"date":41,"type":39},"2025-04-02",{"date":43,"type":20},"2027-05-31",{"name":45,"class":46},"FBD Biologics Limited","INDUSTRY",7,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},"100507848","phase-1-a-safety-and-efficacy-study-of-hcb101-fc-fusion-protein-targeting-sirp-cd47-pathway-in-solid-or-hematological-tumors-100507848","NCT05892718","A Safety and Efficacy Study of HCB101, Fc-fusion Protein Targeting SIRPα-CD47 Pathway, in Solid or Hematological Tumors","A Phase 1, Open-label, Multi-center, Dose Escalation Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Anti-tumor Activity of HCB101 in Subjects With Advanced Solid Tumors or Relapsed and Refractory Non-Hodgkin Lymphoma","Inclusion Criteria:\n\n1. Able to understand and willing to sign the ICF.\n2. Male and female subjects of ≥18 years of age.\n3. Histologically\u002Fcytologically confirmed, locally advanced solid tumor: subjects with histologically or cytologically confirmed advanced solid tumors refractory to standard therapy, or for which no standard treatment exists or non-Hodgkin lymphoma, relapsed or refractory to at least 2 prior lines of therapy.\n4. For subjects with advanced solid tumor - must have at least 1 measurable lesion as defined by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 at baseline.\n5. For subjects with non-Hodgkin lymphoma - must have non-Hodgkin lymphoma that is measurable or assessable for response per Lugano Classification (with 2016 refinement).\n6. Must have ECOG performance status of 0 to 2 at Screening.\n7. Able to provide tumor tissue samples.\n8. Have life expectancy of ≥12 weeks.\n\nExclusion Criteria:\n\n1. With known history of hypersensitivity to any components of HCB101.\n2. Known active or untreated CNS metastases and\u002For carcinomatous meningitis.\n3. Have undergone a major surgery or radical radiotherapy or palliative radiotherapy or have used a radioactive drug that is not completed at least 2 weeks prior to the first dose of HCB101.\n4. Clinically significant cardiovascular condition.\n5. Any previous treatment-related toxicities which have not recovered to ≤ Grade 1 as evaluated by National Cancer Institute, Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0 or baseline, except alopecia and anemia.\n6. With known inherited or acquired bleeding disorder or bleeding diathesis. .\n7. Have RBC transfusion within 4 weeks prior to Screening.\n8. With a previously documented diagnosis of hemolytic anemia or Evans Syndrome in the last 3 months.\n9. Any investigational or approved systemic cancer therapy.\n10. Active use of vitamin K antagonist anticoagulant like warfarin. Use of low molecular weight heparin and factor Xa inhibitors will be permitted on case by case basis. There will be no restriction for daily aspirin ≤ 81 mg\u002FQD.\n11. Have used herbal medication within 14 days prior to the first dose of HCB101.\n12. Have received any treatment targeting the CD47 or SIRPα pathway.\n13. Have other malignancies requiring treatment within 2 years prior to the first dose of HCB101.\n14. Participation in another clinical study with an investigational product administered in the last 14 days prior to receiving the first dose of HCB101.\n15. An investigational device used within 28 days prior to the first dose of HCB101.\n16. Positive for hepatitis B, active hepatitis C infections, positive for HIV, or known active or latent tuberculosis.\n17. Known to have a history of alcoholism or drug abuse.",{"count":56,"type":20},80,[23],"The purpose of this study is to find out whether IV injection of HCB101 is an effective treatment for different types of advanced solid tumors or relapsed and refractory non-Hodgkin lymphoma and what side effects (unwanted effects) may occur in subjects aged 18 years old and above.",[26,60],"Refractory Non-Hodgkin Lymphoma",[29,30,62,63,64],"SIRPα","Solid Tumor","Lymphoma","2026-02-02",{"date":67,"type":39},"2026-02-04",{"date":69,"type":39},"2023-10-02",{"date":71,"type":20},"2029-11-15",{"name":45,"class":46},8,""]