跳至主要内容
临床试验/NCT04155749
NCT04155749进行中(未招募)1 期

Master Protocol for the Phase 1 Study of Cell Therapies for the Treatment of Patients With Relapsed Refractory Multiple Myeloma, Including Long-term Safety Follow-up

Kite, A Gilead Company4 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2019年12月23日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
40
试验地点
4
主要终点
Establish the RP2D of the investigational agent

研究概览

简要总结

Master protocol for cell therapy, Phase 1 proof-of-concept studies in relapsed and refractory multiple myeloma and includes long-term safety follow-up.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Relapsed and refractory Multiple Myeloma treated with at least 3 prior regimens of system therapy including Proteosome Inhibitor (PI), immunomodulatory drugs (IMiD), and anti-CD38 antibody (CD38mab); or has "triple-refractory" disease
  • Documented measurable disease
  • Adequate organ function
  • Life expectancy > 12 weeks, Eastern Cooperative Group Performance Status 0-1

排除标准

  • Plasma Cell Leukemia or History of Plasma Cell Leukemia
  • Patients with a history of severe hypersensitivity to DMSO should be excluded
  • Contraindication to fludarabine or cyclophosphamide
  • Severe uncontrolled intercurrent illness (e.g., infection) or laboratory abnormalities
  • Active central nervous system disease involvement by malignancy or active CNS pathology

研究组 & 干预措施

ARM 1

Experimental

Phase I study of BCMA-specific CAR-modified T-cell therapy using alternative binding domain, for the treatment of patients with relapsed and refractory multiple myeloma

干预措施: anitocabtagene-autoleucel (Drug)

结局指标

主要结局

Establish the RP2D of the investigational agent

时间窗: 24 months

Incidence of treatment-emergent adverse events (TEAEs), including DLT(s)

时间窗: 24 months

次要结局

  • Overall Response Rate (ORR) by IMWG Consensus Criteria(24 months)
  • PK Parameter for Anitocabtagene-Autoleucel: Cmax(Day 1 up to 24 months)
  • PK Parameter for Anitocabtagene-autoleucel: Tmax(Day 1 up to 24 months)
  • PK Parameter for Anitocabtagene-Autoleucel: Area under the curve (AUC)(Day 1 up to 24 months)
  • Best overall response (BOR) by International Myeloma Working Group (IMWG) Consensus Criteria(24 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

Loading locations...

相似试验