[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100643142":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":31,"centralContacts":40,"locations":46,"responsibleParty":65,"collaborators":67,"id":71,"slug":72,"hasResults":73,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":31,"eligibilityCriteria":77,"healthyVolunteers":73,"sex":78,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":31,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":31,"overallStatus":90,"whyStopped":31,"lastUpdateSubmitDate":91,"lastUpdatePostDateStruct":92,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":100},{"fullName":5,"class":6},"Eighth Affiliated Hospital, Sun Yat-sen University","OTHER",[8,14,20],{"label":9,"type":10,"description":11,"interventionNames":12},"phase 1：CG-BM1 Dose Escalation Cohorts","EXPERIMENTAL","Participants will be sequentially assigned to one of three dose cohorts using a \"3+3\" design: low-dose (1\\*10\\^6 cells\u002Fkg), medium-dose (2.0\\*10\\^6 cells\u002Fkg), or high-dose 4.0\\*10\\^6 cells\u002Fkg). In each cohort, CG-BM1 will be administered via intravenous infusion once weekly for a total of 4 doses on Days 0, 7, 14, and 21. All participants across all cohorts will concurrently receive standard background therapy consisting of celecoxib 0.2g orally once daily.",[13],"Biological: IV administration of CG-BM1",{"label":15,"type":16,"description":17,"interventionNames":18},"phase 2 ：placebo Cohorts","PLACEBO_COMPARATOR","Participants will be randomized to receive the placebo (Compound Electrolyte Injection) via intravenous (IV) infusion once weekly for a total of 4 doses, mimicking the regimen of the experimental group. All participants will simultaneously receive a background therapy of celecoxib 0.2g orally once daily.",[19],"Biological: Placebo",{"label":21,"type":10,"description":22,"interventionNames":23},"phase 2 ：CG-BM1 Cohorts","Participants will be randomized to receive CG-BM1 at the clinically recommended dose (determined by the Safety Review Committee based on Phase 1 results) via intravenous (IV) infusion once weekly for a total of 4 doses. All participants will simultaneously receive a background therapy of celecoxib 0.2g orally once daily.",[24],"Biological: CG-BM1",[26,32,36],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"BIOLOGICAL","IV administration of CG-BM1","Dose level 1: CG-BM1 1.0×10⁶ cells\u002Fkg, IV, weekly × 4 + celecoxib, 0.2g, p.o. daily Dose level 2: CG-BM1 2.0×10⁶ cells\u002Fkg, IV, weekly × 4 + celecoxib, 0.2g, p.o. daily Dose level 3: CG-BM1 4.0×10⁶ cells\u002Fkg, IV, weekly × 4 + celecoxib, 0.2g, p.o. daily",[9],null,{"type":27,"name":33,"description":34,"armGroupLabels":35,"otherNames":31},"Placebo","Sodium Chloride Solution, 5 ml, IV, weekly × 4+ celecoxib, 0.2g, p.o. daily",[15],{"type":27,"name":37,"description":38,"armGroupLabels":39,"otherNames":31},"CG-BM1","CG-BM1 \\[recommended dose\\], IV, weekly × 4 + celecoxib, 0.2g, p.o. daily",[21],[41],{"name":42,"role":43,"phone":44,"phoneExt":31,"email":45},"Prof.Wang","CONTACT","86+138 2602 4785","wangp57@mail.sysu.edu.cn",[47],{"facility":48,"status":31,"city":49,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":60},"The Eighth Affiliated Hospital, Sun Yat-sen University","Shenzhen","Guangdong","518033","China","CN",{"type":55,"coordinates":56},"Point",[57,58],114.0683,22.54554,{"lat":58,"lon":57},[61],{"name":62,"role":43,"phone":63,"phoneExt":31,"email":64},"Prof. Chen","86+83982222","sysuehoffice@mail.sysu.edu.cn",{"type":66,"investigatorFullName":31,"investigatorTitle":31,"investigatorAffiliation":31,"oldNameTitle":31,"oldOrganization":31},"SPONSOR",[68],{"name":69,"class":70},"Guangzhou Cellgenes Biotechnology Co.,Ltd","UNKNOWN","100643142","phase-1-safety-and-efficacy-of-allogeneic-bone-marrow-mscs-in-ankylosing-spondylitis-100643142",false,"NCT07632599","Safety and Efficacy of Allogeneic Bone Marrow MSCs in Ankylosing Spondylitis","An Early Exploratory Clinical Study on the Safety and Preliminary Efficacy of Allogeneic Human Bone Marrow Mesenchymal Stem Cells in Patients With Ankylosing Spondylitis","Inclusion Criteria:\n\n* Meet the diagnostic criteria for ankylosing spondylitis (AS)\n* Age 18 to 40 years\n* Must be able to understand and communicate with the investigator, comply with study requirements, and provide signed and dated informed consent before any study assessments are performed\n* Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) total score ≥ 4 (0-10 scale), and total back pain measured by VAS ≥ 40 mm (0-100 mm)\n* CRP or ESR elevated ≥ 1.5 times the upper limit of normal\n* Patients taking methotrexate (≤ 25 mg\u002Fweek) or sulfasalazine (≤ 3 g\u002Fday) are permitted to continue these medications, provided they have been used for at least 3 months and maintained at a stable dose for at least 4 weeks prior to randomization. Patients taking methotrexate must maintain stable folic acid supplementation prior to randomization\n* Patients taking DMARDs other than methotrexate and sulfasalazine must discontinue them at least 4 weeks prior to randomization\n* No prior use of any form of biologics within 6 months\n* Spinal X-ray must rule out complete rigid ankylosis\n\nExclusion Criteria:\n\n* Known allergy to any component of the study drug (primarily bone marrow mesenchymal stem cells; excipients include dimethyl sulfoxide, human albumin, etc.)\n* Current evidence of infection or malignancy as shown by chest X-ray or MRI within 3 months prior to screening\n* Currently using potent opioid analgesics\n* Received any intra-articular injection therapy (e.g., corticosteroids) within 4 weeks prior to randomization\n* Received any intramuscular corticosteroid injection within 2 weeks prior to randomization\n* Received traditional Chinese medicine treatment for AS within 4 weeks prior to randomization\n* Pregnant or breastfeeding women\n* Presence of underlying metabolic, hematologic, renal, hepatic, pulmonary, neurologic, endocrine, cardiac, infectious, or gastrointestinal disease that, in the investigator's opinion, would place the patient at unacceptable risk if treated with immunomodulatory agents\n* Significant health problem or disease including (but not limited to): uncontrolled hypertension (≥ 160\u002F95 mmHg), congestive heart failure, uncontrolled diabetes, or extremely poor functional status rendering the patient unable to care for themselves\n* History of renal impairment, glomerulonephritis, or a single kidney, or serum creatinine level \\> 1.5 mg\u002FdL\n* Active systemic infection within 2 weeks prior to randomization (common cold excluded)\n* Current infection or history of chronic, recurrent infectious disease, or clinical test suggesting tuberculosis (including latent tuberculosis)\n* Known HIV infection, hepatitis B, or hepatitis C at screening or randomization\n* History or evidence of alcohol or drug abuse within 6 months prior to randomization\n* History of lymphoproliferative disease or known malignancy of any organ system within the past 5 years\n* Pulmonary arterial hypertension class III or IV (WHO functional classification) at screening\n* History of deep vein thrombosis at screening, or history of pulmonary embolism within 3 months prior to screening\n* Any other condition that, in the investigator's opinion, makes the patient unsuitable for participation in the study (e.g., lack of compliance, difficulty in long-term follow-up)","ALL","18 Years","40 Years",{"count":82,"type":83},40,"ESTIMATED","INTERVENTIONAL",[86],"PHASE1","The goal of this clinical trial is to learn if allogeneic human bone marrow-derived mesenchymal stem cells (CG-BM1) are safe and show preliminary efficacy in treating patients with ankylosing spondylitis (AS). It will also explore the appropriate dose of CG-BM1.\n\nThe main questions it aims to answer are:\n\nWhat medical problems (adverse events) do participants have when taking CG-BM1? (Safety and tolerability)\n\nDoes CG-BM1 improve disease activity, pain, and function in patients with AS? (Preliminary efficacy)\n\nResearchers will compare CG-BM1 to a placebo (an inactive substance that looks like CG-BM1) in the second phase of the study to see if CG-BM1 works for AS.\n\nThis study has two phases:\n\nPhase 1 (dose-escalation): Open-label, single-arm. Participants will receive one of three escalating doses of CG-BM1 weekly for 4 weeks.\n\nPhase 2 (dose-expansion): Randomized, double-blind, placebo-controlled. Participants will receive either the recommended dose of CG-BM1 or a placebo weekly for 4 weeks, in addition to standard background therapy (celecoxib).\n\nParticipants will:\n\nReceive CG-BM1 or placebo via intravenous infusion once a week for 4 weeks\n\nVisit the clinic for follow-up assessments at Week 1, 4, 8, 12, and 24 after the first infusion\n\nUndergo physical exams, laboratory tests (blood and urine), and complete questionnaires about disease activity, pain, and function (e.g., BASDAI, VAS, ASAS response criteria)",[89],"Ankylosing Spondylitis","NOT_YET_RECRUITING","2026-06-02",{"date":93,"type":94},"2026-06-08","ACTUAL",{"date":96,"type":83},"2026-07-01",{"date":98,"type":83},"2027-06-01",{"name":5,"class":6},1]