Selinexor
Selinexor 是目前在国外临床研究中出现的一款新药或疗法,主要研究方向为Myelofibrosis、Post-polycythemia Vera Myelofibrosis、Post-essential Thrombocythemia Myelofibrosis。下面汇总了它当前在全球正在招募患者的研究,以及中国患者可以走的申请途径。
24 项
全球在招研究
5 项
已进入 III/IV 期
14 个
开展国家和地区
有
中国境内设点
药品与企业信息
研发企业
- John Mascarenhas
- National Cancer Institute (NCI)
- Oncotherapeutics
- Washington University School of Medicine
- Tianjin Medical University Cancer Institute and Hospital
- Fudan University
- Beijing Friendship Hospital
- Hackensack Meridian Health
汇总自相关试验登记的主要申办方;研究机构申办时会显示相应机构名称。
生产企业
公开药品批准资料或正式说明书暂未提供明确的生产企业信息。
研发企业与生产企业可能不是同一家。研究阶段药品可能尚未公布生产企业;生产企业仅取自美国上市原研药说明书所列企业(不含仿制药),不作推测;仅在其他国家上市的药品暂无法显示。
主要开展国家和地区
美国、中国、意大利、Greece、Israel、西班牙、加拿大、比利时、Bulgaria、Czechia、丹麦、法国
正在招募患者的 Selinexor 研究
Testing Atezolizumab With Selinexor in People ≥ 12 Years Old With Alveolar Soft Part Sarcoma, AXIOM Trial
II 期招募中美国NCT05333458A Trial of Selinexor, Ruxolitinib and Methylprednisolone
I 期招募中美国NCT06225310Selinexor Maintenance Post CAR-T Cell Therapy for Multiple Myeloma
I 期招募中美国NCT07200102Second-line Immunotherapy for ES-SCLC
不适用招募中中国NCT06853678A Phase Ib/II Clinical Study Evaluating the Safety and Efficacy of Tislelizumab in Combination With Golidocitinib and Selinexor for the Treatment of R/R NKTCL
I 期 / II 期招募中中国NCT06966154Golidocitinib Combined With Selinexor for CAEBVD
II 期 / III 期招募中中国NCT07369739A Study of Selinexor, in Combination With Carfilzomib, Daratumumab or Pomalidomide in Patients With Multiple Myeloma
II 期招募中美国NCT04661137A Multicenter, Randomized, Open-label, Parallel-group, Controlled, Superiority Phase III Clinical Study Comparing the Efficacy and Safety of F182112 Versus Standard of Care in Patients With Relapsed or Refractory Multiple Myeloma
III 期招募中中国NCT07579234Study of Selinexor With Carfilzomib, Isatuximab and Dexamethasone for Patients With Relapsed and/or Refractory Multiple Myeloma
I 期 / II 期招募中美国NCT07479979HCMT/MM2401: Ph2 Study of Selinexor + Bispecific Antibody for RRMM
II 期招募中美国NCT06822972A Study in Participants With Relapsed or Refractory Multiple Myeloma for IBI3003
III 期招募中中国NCT07623798Clinical Study of XPO1 Inhibitor Selinexor Combined With COPL in Newly Diagnosed Advanced NK/T-cell Lymphoma
II 期招募中中国NCT05833893Selinexor, High-dose Methotrexate, and Rituximab Combined With Radiotherapy for Newly Diagnosed, Transplant-ineligible Patients With Central Nervous System Lymphoma: An Open-label, Single-arm, Multicenter Phase II Study
II 期招募中中国NCT07002099Observational Study on the Combination of Selinexor With Bortezomib and Dexamethasone for the Treatment of MM Patients
不适用招募中意大利NCT06933277A Study of Selinexor (Seli) + Low-dose Dexamethasone (LDD) in Penta-refractory Multiple Myeloma (MM), Seli and Bortezomib + LDD in Triple-class Refractory MM.
II 期招募中GreeceIsraelNCT04414475Predicting Response to Selinexor-Based Therapy in Relapsed/Refractory Multiple Myeloma: A Multicenter Prospective Study
不适用招募中中国NCT07514052A Study of Selinexor in People With Wilms Tumors and Other Solid Tumors
II 期招募中美国NCT05985161Selinexor Plus Gemcitabine in Selected Advanced Soft-tissue Sarcoma (SeliSarc)
II 期招募中西班牙NCT06114004Pomalidomide, Anti-PD-1 Antibody Combined With Selinexor (PPS) in Relapsed/Refractory Primary Central Nervous System Diffuse Large B-Cell Lymphoma
II 期招募中中国NCT07523737A Phase III Clinical Study of Purinostat Mesylate for Injection in Patients With Diffuse Large B-cell Lymphoma
III 期招募中中国NCT07011056Selinexor and Backbone Treatments of Multiple Myeloma Patients
I 期 / II 期招募中美国加拿大NCT02343042Decitabine and Selinexor in Combination to Reverse Drug Resistance With Standard Chemotherapy in Ovarian Cancer
II 期招募中美国NCT05983276A Study Comparing QLS32015 Monotherapy Versus Pomalidomide, Dexamethasone (Pd) or Selinexor, Dexamethasone (Sd) in Participants With Relapsed or Refractory Multiple Myeloma
III 期招募中中国NCT07138209A Study of Selinexor Monotherapy in Subjects With JAK Inhibitor-naïve Myelofibrosis and Moderate Thrombocytopenia
II 期招募中美国比利时Bulgaria加拿大NCT05980806
中国患者怎么争取用上这款药
这款药已经有研究在中国境内设点,可以先带完整病历去对应医院咨询入组;同时也可以并行了解下面几条途径,多一条备选。
查看完整申请指南同类方向的其他在研新药
本页信息整理自 ClinicalTrials.gov 公开登记数据,仅供参考,不构成医疗建议;是否适合使用该药物,请以专业医生和研究团队的意见为准。