[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100627221":3},{"organization":4,"armGroups":7,"interventions":36,"overallOfficials":55,"centralContacts":60,"locations":66,"responsibleParty":82,"collaborators":42,"id":84,"slug":85,"hasResults":86,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":42,"eligibilityCriteria":90,"healthyVolunteers":91,"sex":92,"minAge":93,"maxAge":94,"enrollmentInfo":95,"targetDuration":42,"studyType":98,"phases":99,"briefSummary":89,"conditions":101,"keywords":103,"overallStatus":107,"whyStopped":42,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":117},{"fullName":5,"class":6},"Lanzhou Institute of Biological Products Co., Ltd","INDUSTRY",[8,14,17,21,26,29,32],{"label":9,"type":10,"description":11,"interventionNames":12},"Group 1：40 IU\u002Fkg monoclonal antibody - Monotherapy Study","EXPERIMENTAL","60 trial participants were enrolled and randomly assigned at a 1:1:1 ratio to the 40 IU\u002Fkg monoclonal antibody group (20 participants), the HRIG control group (20 participants), and the 80 IU\u002Fkg monoclonal antibody group (20 participants).",[13],"Drug: Recombinant Human Rabies Virus Monoclonal Antibody Injection",{"label":15,"type":10,"description":11,"interventionNames":16},"Group 2: 80 IU\u002Fkg monoclonal antibody - Monotherapy Study",[13],{"label":18,"type":10,"description":11,"interventionNames":19},"Group 3: HRIG (20 IU\u002Fkg) group - Monotherapy Study",[20],"Drug: Human Rabies Immunoglobulin (HRIG)",{"label":22,"type":10,"description":23,"interventionNames":24},"Group 4：40 IU\u002Fkg monoclonal antibody plus vaccine - Combined Administration Study","A total of 140 trial participants were enrolled and randomly assigned in a 2:2:2:1 ratio to the following groups:\n\n40 IU\u002Fkg monoclonal antibody plus vaccine group (40 participants)\n\nHRIG plus vaccine group (40 participants)\n\n80 IU\u002Fkg monoclonal antibody plus vaccine group (40 participants)\n\nPlacebo plus vaccine group (20 participants).",[13,25],"Biological: Rabies Vaccine",{"label":27,"type":10,"description":23,"interventionNames":28},"Group 5：80 IU\u002Fkg monoclonal antibody plus vaccine - Combined Administration Study",[13,25],{"label":30,"type":10,"description":23,"interventionNames":31},"Group 6: HRIG (20 IU\u002Fkg) plus vaccine - Combined Administration Study",[20,25],{"label":33,"type":10,"description":23,"interventionNames":34},"Group 7: placebo plus vaccine - Combined Administration Study",[35,25],"Drug: Placebo",[37,43,47,50],{"type":38,"name":39,"description":40,"armGroupLabels":41,"otherNames":42},"DRUG","Recombinant Human Rabies Virus Monoclonal Antibody Injection","On Day 0, administer via intramuscular injection into the lateral thigh. It is strictly prohibited to use the same syringe as the rabies vaccine or to co-administer at the same injection site.",[9,15,22,27],null,{"type":38,"name":44,"description":45,"armGroupLabels":46,"otherNames":42},"Human Rabies Immunoglobulin (HRIG)","On Day 0, administration shall be performed via intramuscular injection into the lateral aspect of the thigh. It is strictly prohibited to use the same syringe as the rabies vaccine or to administer both agents at the same injection site.",[18,30],{"type":38,"name":48,"description":45,"armGroupLabels":49,"otherNames":42},"Placebo",[33],{"type":51,"name":52,"description":53,"armGroupLabels":54,"otherNames":42},"BIOLOGICAL","Rabies Vaccine","On Days 0, 3, 7, 14, and 28, administer via intramuscular injection into the deltoid muscle of the upper arm. Injection into the gluteal region is prohibited. The injection on Day 0 should be administered as soon as possible after the administration of the investigational product.",[22,27,30,33],[56],{"name":57,"affiliation":58,"role":59},"Chaolin Huang","Wuhan Jinyintan Hospital","PRINCIPAL_INVESTIGATOR",[61],{"name":62,"role":63,"phone":64,"phoneExt":42,"email":65},"Jijun Chen","CONTACT","+86 13919275320","chenjijun@sinopharm.com",[67],{"facility":68,"status":42,"city":69,"state":70,"zip":71,"country":72,"countryCode":73,"cosmosGeoPoint":74,"geoPoint":79,"contacts":80},"Lanzhou Institute of Biological Products Co., Ltd.","Lanzhou","Gansu","730000","China","CN",{"type":75,"coordinates":76},"Point",[77,78],103.83987,36.05701,{"lat":78,"lon":77},[81],{"name":62,"role":63,"phone":64,"phoneExt":42,"email":65},{"type":83,"investigatorFullName":42,"investigatorTitle":42,"investigatorAffiliation":42,"oldNameTitle":42,"oldOrganization":42},"SPONSOR","100627221","phase-2-a-phase-ii-trial-of-a-recombinant-human-anti-rabies-virus-monoclonal-antibody-100627221",false,"NCT07445815","A Phase II Trial of a Recombinant Human Anti-Rabies Virus Monoclonal Antibody","A Phase II, Single-Center, Randomized, Blinded, Controlled Clinical Trial to Evaluate the Safety, Tolerability, and Pharmacodynamics of a Recombinant Human Anti-Rabies Virus Monoclonal Antibody Injection in Healthy Subjects","Inclusion Criteria:\n\n1. Healthy individuals aged 18-60 years (inclusive), regardless of gender, capable of providing valid legal identification.\n2. Participants voluntarily agree to participate in the study and sign an informed consent form.\n3. Female participants must have no plans for pregnancy or egg donation from 14 days prior to dosing until 6 months after dosing and must voluntarily adopt effective physical contraceptive measures. Male participants must have no plans for pregnancy or sperm donation within 6 months after dosing and must voluntarily adopt effective physical contraceptive measures.\n4. Female participants must weigh ≥45.0 kg and ≤80.0 kg, and male participants must weigh ≥50.0 kg and ≤80.0 kg. Body mass index (BMI) must be between 18.0 and 26.0 kg\u002Fm² (inclusive) (BMI = weight in kg \u002F height in m²).\n5. Vital signs (reference ranges: systolic blood pressure 90-140 mmHg, diastolic blood pressure 60-90 mmHg, pulse rate 50-100 beats per minute, all inclusive; body temperature assessed by the investigator according to the research center's standards), physical examination, and clinical laboratory and auxiliary tests during the screening period must be normal or judged by the investigator to have no clinical significance if abnormal.\n\nExclusion Criteria:\n\n1. Known allergy to the investigational product (including excipients or similar drugs), or individuals with a history of severe allergic diseases or considered allergic constitution (e.g., allergies to two or more drugs, foods, or pollen) as judged by the investigator to potentially compromise participant safety.\n2. Clear history of allergy to essential substances that may be encountered during the trial (e.g., skin disinfectants).\n3. History of clinically severe diseases within the 6 months (180 days) prior to screening that remain unresolved, or current acute or chronic illnesses that may significantly affect the metabolism or safety evaluation of the investigational product.\n4. History of autoimmune diseases or chronic hepatitis.\n5. History of seizures, epilepsy, psychiatric or neurological disorders, or family history of seizures or epilepsy.\n6. Major surgery within the 3 months (90 days) prior to screening, or surgery that may significantly affect the metabolism or safety evaluation of the investigational product.\n7. Previous vaccination with human rabies vaccine, or suspected history of rabies exposure (defined as bites, scratches, licks on mucous membranes or broken skin by rabid, suspected rabid, or undetermined rabies status animals, or direct contact of open wounds or mucous membranes with saliva or tissues potentially containing rabies virus), as determined by inquiry.\n8. Positive screening for anti-rabies virus antibodies during the screening period.\n9. Vaccination with any vaccine other than the rabies vaccine within the 1 month (30 days) prior to screening.\n10. Use of other antibody-based drugs or immunoglobulins within the 3 months (90 days) prior to screening.\n11. Use of passive immunizing agents, immunosuppressants, or corticosteroids within the 3 months (90 days) prior to screening.\n12. Use of medications that may affect the metabolism or safety evaluation of the investigational product within the 14 days prior to screening or ongoing use of such medications.\n13. Participation in any clinical trial involving the use of investigational drugs or devices within the 3 months (90 days) prior to screening, or planned participation in other clinical trials during this study.\n14. Regular alcohol consumption within the 3 months (90 days) prior to screening, averaging more than 2 alcohol units per day (1 unit = 17.7 mL ethanol, equivalent to 357 mL of 5% beer, 43 mL of 40% spirits, or 147 mL of 12% wine), or inability to abstain from alcohol during the trial period.\n15. Smoking habit within the 3 months (90 days) prior to screening (more than 5 cigarettes or equivalent tobacco per day), or inability to abstain from smoking during the trial period.\n16. Blood loss\u002Fdonation exceeding 300 mL (excluding physiological blood loss in females) within the 3 months (90 days) prior to screening, receipt of blood transfusions or blood products, or plans to donate blood within 1 month (30 days) after the trial.\n17. Inability to avoid strenuous exercise within 14 days after dosing.\n18. History of drug abuse.\n19. Pregnant or breastfeeding women.\n20. History of needle or blood phobia, poor vascular condition, or intolerance to venipuncture.\n21. Participants who may be unable to cooperate in completing the study for other reasons or are deemed unsuitable for inclusion by the investigator.",true,"ALL","18 Years","60 Years",{"count":96,"type":97},200,"ESTIMATED","INTERVENTIONAL",[100],"PHASE2",[102],"Rabies (Healthy Volunteers)",[104,105,106],"Recombinant Human","Rabies","Monoclonal Antibody","NOT_YET_RECRUITING","2026-02-25",{"date":110,"type":111},"2026-03-03","ACTUAL",{"date":113,"type":97},"2026-01-31",{"date":115,"type":97},"2026-08-21",{"name":5,"class":6},1]