跳至主要内容
临床试验/NCT06370013
NCT06370013Available不适用

An Open Label, Multicenter Rollover Study for Continued Characterization of Safety and Tolerability of TT-00420 (Tinengotinib) Tablet Monotherapy in Adult Patients With Advanced Solid Tumors

TransThera Sciences (Nanjing), Inc.5 个研究点 分布在 1 个国家开始时间: 2024年4月17日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
Available
试验地点
5

研究概览

简要总结

This study is an open-label, multicenter study for Continued Characterization of Safety and Tolerability of TT-00420 (tinengotinib) Tablet Monotherapy in Adult Patients with Advanced Solid Tumors

详细描述

This is a Rollover study. Only subjects who continue to receive clinical benefit from continuation of tinengotinib monotherapy and are tolerating tinengotinib at the time of enrollment are eligible to participate on this study. Subjects on this rollover study may continue to receive tinengotinib at the dose that they were previously receiving on the TransThera parent study and may continue for as long as the subject continues to benefit from treatment.

研究设计

研究类型
Expanded Access

入排标准

性别
All
接受健康志愿者

入选标准

  • Subject is currently enrolled in a pre-defined TransThera-sponsored parent study and is receiving tinengotinib as a single agent.
  • Subject is currently deriving clinical benefit from the study treatment, as determined by the investigator.

排除标准

  • Subject has been permanently discontinued from tinengotinib in the parent protocol for any reason other than enrollment in the Rollover study
  • Subject does not meet the criteria specified in the parent protocol for continued treatment on study.

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (5)

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