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临床试验/NCT06798298
NCT06798298招募中不适用

A Long-Term Follow-up Protocol for Participants Treated With Gene Modified T Cells

Regeneron Pharmaceuticals2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年11月10日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
2
主要终点
Incidence of delayed adverse events considered at least possibly related to prior gene modified T cell therapy

研究概览

简要总结

This is a prospective study for the Long-Term Follow-Up (LTFU) of safety and efficacy of all participants exposed to gene modified (GM) T cell therapy in accordance with Health Authorities' guidance for participants treated with gene therapy products.

Participants who received at least one infusion of gene modified T cells in a 2seventy bio (prior to April 2024) or Regeneron Pharmaceuticals sponsored study will be asked to participate in this LTFU protocol, upon either premature discontinuation from, or completion of the parent treatment protocol.

Participants enrolled in this LTFU protocol will have safety assessments, laboratory evaluations, and complete patient-reported outcome (PRO) questionnaires at scheduled intervals as applicable.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • All participants who received at least one GM T cell infusion in a previous 2seventy bio (prior to April 2024) or Regeneron Pharmaceuticals sponsored study, and have completed the post-treatment follow-up period on the parent treatment protocol, or discontinued follow-up on the parent protocol after completing at least 6 months of safety monitoring, as applicable.
  • Participant (and legal representative, when applicable) must understand and voluntarily sign an Informed Consent Form (ICF)/Informed Assent Form (IAF) prior to any study related assessments/procedures being conducted.

排除标准

  • Not applicable.

结局指标

主要结局

Incidence of delayed adverse events considered at least possibly related to prior gene modified T cell therapy

时间窗: Up to 15 years

Persistence of gene modified T cells

时间窗: Up to 15 years

Analysis of vector integration sites

时间窗: Up to 15 years

Incidence of RCL

时间窗: Up to 15 years

Disease progression status

时间窗: Up to 15 years

To assess long-term efficacy following treatment with gene modified T cells

Date of disease progression

时间窗: Up to 15 years

Survival status

时间窗: Up to 15 years

次要结局

  • Health-Related Quality of Life (HRQoL) Changes(Up to 5 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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