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Selinexor in Combination With Thalidomide and Dexamethasone in RRMM

2021年5月13日 更新者:Li Zheng

Phase Ib/II Study of ATG-010 in Combination With Thalidomide and Dexamethasone for Relapsed/Refractory Multiple Myeloma

Multiple myeloma (MM) is an incurable plasma cell cancer that almost all patients eventually relapse despite advancement in treatment strategies. B-cell maturation antigen (BCMA) is a cell surface receptor that expressed primarily by malignant and normal plasma cells. This is a single-arm that includes escalation phase and expansion phase ,Selinexor in Combination withThalidomide and Dexamethasone to Treat Relapsed/Refractory Multiple Myeloma Patients.To evaluate efficacy and safety of Selinexor in combination with Thalidomide and Dexamethasone in RRMM patients received at least one prior lines of therapy

研究概览

详细说明

This is a single-arm and open-label phase Ib/IIa study of Relapsed/Refractory Multiple Myeloma patients who have received at least one prior lines of treatment therapy; Approximately 3-48 patients will be enrolled in the study. In dose escalation phase, patients with RRMM will be treated with thalidomide 100mg/d, dexamethasone 20mg biweekly, and escalating doses of oral ATG-010 weekly in a 3+3 design. ATG-010 dose level (DL) 1, 2 and 3 are 60, 80 and 100mg respectively.

Then a phase 2 expansion at the recommended dose level based on phase 1b trial will be conducted to evaluate the efficacy, safety and tolerability.

This arm is 4 weeks per cycle and include a total of 12 cycles.Selinexor RP2D,Thalidomide will be given at 100mg/d d1-28, and Dexamethasone 20 mg/d will be given on day 1, 2,8,9,15,16,22,23. If a patient develops partial intolerance to glucocorticoids (as determined by the Investigator) during the study, a dose reduction of dexamethasone maximum to 10 mg is permitted. If patients do not tolerate this dose, a potential discontinuation or further dose reduction would be allowed.

研究类型

介入性

注册 (预期的)

48

阶段

  • 阶段2
  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Sichuan
      • Chengdu、Sichuan、中国、610041
        • West China Hospital of Sichuan University
        • 接触:
        • 首席研究员:
          • Ting Niu, M.D.,Ph.d
        • 首席研究员:
          • Li Zheng, M.D.,Ph.d

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 75年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Patients must meet all of the following inclusion criteria to be eligible to enroll in this study:

    1. Known and written informed consent (ICF) voluntarily.
    2. Age ≥ 18 years and ≤ 75 years.
    3. Patients with multiple myeloma who have received first-line treatment (induction, autologous transplantation and maintenance as the same first-line treatment) and achieved at least partial remission in induction.
    4. At or after accepting first-line regimen, subjects must have progression disease (PD) recorded which is determined by researcher according to IMWG criteria.
    5. Any clinically significant non-hematological toxicities (except for hair loss, peripheral neuropathy, which is otherwise stipulated in Article 13 of the exclusion criteria) that relevant to previous therapies must have resolved to ≤Grade 2 prior to first dose of study drug.
    6. Adequate hepatic function: total bilirubin < 2× upper limit of normal (ULN) (for patients with Gilbert's syndrome, a total bilirubin of < 3× ULN is required), AST < 2.5× ULN, and ALT < 2.5× ULN.
    7. Adequate renal function: estimated creatinine clearance ≥ 20 mL/min (calculated using the formula of Cockroft-Gault).
    8. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2.
    9. Measurable MM as defined by at least one of the following:

      1. Serum M-protein (SPEP) ≥ 10 g/L
      2. 24 hours-Urinary M-protein excretion ≥ 0.2 g (200 mg)
      3. Serum FLC ≥ 100 mg/L with abnormal FLC ratio
    10. Expected survival is more than 6 months.
    11. Adequate hematopoietic function (no blood transfusion within 2 weeks and no G-CSF/GM-CSF supportive treatment within 1 week prior to screening test):

      1. Hemoglobin level ≥ 80 g/L
      2. ANC ≥ 1,000/mm3 (1.0×109/L)
      3. Platelet count ≥ 75,000/mm3 (75×109/L)
    12. Female patients of childbearing potential must meet below two criteria:

      1. must agree to use effective contraception methods since signature in ICF, throughout the study and for 3 months following the last dose of study treatment.
      2. must have a negative serum pregnancy test at screening. Note: A woman is considered of childbearing potential following menarche and until becoming postmenopausal (defined as no menstrual period for a minimum of 12 months) or permanently sterile (having undergone a hysterectomy, bilateral salpingectomy or bilateral oophorectomy). A woman who is taking oral contraceptive or using intrauterine device is considered of childbearing potential.
    13. Male patients (including those who have received vasectomy) must use a condom if sexually active with a female of child-bearing potential throughout the study and for 3 months following the last dose of study treatment.

Exclusion Criteria:

  • Patients who meet any of the following criteria will not be enrolled:

    1. Asymptomatic (smoldering) MM.
    2. Plasma cell leukemia.
    3. Documented active amyloidosis.
    4. Previously refractory or intolerant to immunomodulators.
    5. Pregnancy or breastfeeding.
    6. Major surgery was performed within 4 weeks prior to the first study.
    7. Patients with active, unstable cardiovascular diseases, fits any of the following:

      1. Symptomatic ischemia, or
      2. Uncontrolled clinically-significant conduction abnormalities (e.g., patients with ventricular tachycardia on antiarrhythmics are excluded; patients with first-degree atrioventricular (AV) block or asymptomatic left anterior fascicular block/right bundle branch block (LAFB/RBBB) are allowed), or
      3. Congestive heart failure (CHF) of New York Heart Association (NYHA) ≥ Grade 3, or
      4. Acute myocardial infarction (AMI) within 3 months prior to the first dose of study drug.
    8. Uncontrolled active infection within 1 week prior to the first dose of study drug.
    9. Known HIV positive.
    10. Known active hepatitis A, B, or C infection; or known positive for HCV RNA or HBsAg.

      (Note: patients with HBsAg negative but HBc Ab positive need further HBV-DNA test, excluded if HBV-DNA ≥103 , if HBV-DNA <103 need anti-viral drugs)

    11. Prior malignancy that required treatment or has shown evidence of recurrence (except for skin basal-cell carcinoma and in-situ carcinoma including squamous cell carcinoma, bladder cancer in situ, endometrial cancer in situ, cervical cancer in situ/atypical hyperplasia, prostate cancer incidental finding (T1a or T1b), or breast cancer in situ) within 5 years prior to the first dose of study drug.
    12. Active GI dysfunction interfering with the ability to swallow tablets, or any GI dysfunction that could interfere with absorption of study treatment.
    13. Grade ≥ 3 peripheral neuropathy, and Grade ≥ 2 painful neuropathy, within 3 weeks prior to the first dose of study drug.
    14. Previous history of deep vein thrombosis.
    15. Serious, active psychiatric, or medical conditions which, in the opinion of the Investigator, could interfere with study treatment.
    16. Participation in an investigational anti-cancer clinical study within 3 weeks or 5 half-lives (T1/2) prior to the first dose of study drug.
    17. Received ASCT within 12 weeks prior to the first dose of study drug or previous allogeneic stem cell transplantation (no time limitation).
    18. Treatment with an approved or trial anticancer drug was given within 4 weeks prior to the first study.
    19. Known intolerance to or contraindication for glucocorticoid therapy.
    20. Prior exposure to a SINE compound.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Selinexor in combination with thalidomide and Dexamethasone
Selinexor in combination with thalidomide and Dexamethasone. Thalidomide will be given at 100mg/d d1-28,and Dexamethasone 20 mg/d will be given on day 1, 2,8,9,15,16,22,23. Treatment will be administered in 28-day cycles,include a total of 12 cycles. Selinexor dose escalation: 60, 80, 100mg respectively on day 1,8,15,22 for 4-week cycles. Then Selinexor will be given at the recommended dose level on phase II.
100 毫克/天,宝。第 1-28 天
其他名称:
  • 烦请听
Selinexor (ATG-010# is a first-in-class, oral selective exportin 1 (XPO1) inhibitor (1,2). Selinexor functions by binding with and inhibiting the nuclear export protein XPO1 (also called CRM1), leading to the accumulation of tumor suppressor proteins in the cell nucleus along with inhibition of translation of oncoprotein mRNAs.
其他名称:
  • ATG-010
20 mg/d Po. on day 1, 2,8,9,15,16,22,23
其他名称:
  • 敏捷

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
总缓解率 (ORR)
大体时间:从第一次研究治疗剂量的日期到 PD 评估的日期最多 12 个月进行评估
每组的 ORR:部分反应 (PR) + 非常好的部分反应 (VGPR) + 完全反应 (CR)
从第一次研究治疗剂量的日期到 PD 评估的日期最多 12 个月进行评估

次要结果测量

结果测量
措施说明
大体时间
无进展生存期 (PFS)
大体时间:12个月
从研究治疗开始到 PD 或死亡(不论原因)的持续时间,以先到者为准
12个月
临床受益率 (CBR)
大体时间:12个月
临床受益率(CBR=ORR+轻微反应 [MR])
12个月
疾病控制率(DCR)
大体时间:12个月
疾病控制率(DCR=CBR+疾病稳定[SD;至少 12 周])
12个月
出现不良事件的参与者人数
大体时间:从首次服用研究药物到治疗结束(最长 12 个月)
发生治疗紧急不良事件 (TEAE) 和治疗紧急严重不良事件 (TESAE) 的参与者人数
从首次服用研究药物到治疗结束(最长 12 个月)
总生存期(OS)
大体时间:12个月
Kaplan-Meier 的估计
12个月
微小残留病 (MRD)
大体时间:12个月
评估 CR 和 sCR 患者的微小残留病灶
12个月
缓解持续时间 (DOR)
大体时间:12个月
从第一次观察到至少 PR 到疾病进展或因疾病进展导致死亡的时间,以先发生者为准。
12个月

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

调查人员

  • 首席研究员:Ting Niu, M.D., Ph.D、West China Hospital
  • 首席研究员:Li Zheng, M.D., Ph.D、West China Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (预期的)

2021年7月6日

初级完成 (预期的)

2024年12月30日

研究完成 (预期的)

2024年12月30日

研究注册日期

首次提交

2021年5月13日

首先提交符合 QC 标准的

2021年5月13日

首次发布 (实际的)

2021年5月18日

研究记录更新

最后更新发布 (实际的)

2021年5月18日

上次提交的符合 QC 标准的更新

2021年5月13日

最后验证

2021年5月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

All IPD results are used for publication,and can be shared with other investigators and sponsors

IPD 共享时间框架

Study Protocol can be shared Starting 12 months after publication

IPD 共享访问标准

Study Protocol must not be shared with non-participants until after publication and must be authorized by the principal investigator and sponsors

IPD 共享支持信息类型

  • 研究方案

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

是的

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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