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临床试验/NCT06099639
NCT06099639No Longer Available不适用

Medical Access Program for Patritumab Deruxtecan (HER3 DXd, U3-1402)

Daiichi Sankyo21 个研究点 分布在 1 个国家开始时间: 2023年10月25日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available
试验地点
21

研究概览

简要总结

The purpose of this Medical Access Program is to provide access to HER3-DXd for eligible patients with NSCLC who, in their treating physician's opinion, have an unmet clinical need which cannot be treated with approved and commercially available drugs and who cannot enter a clinical trial prior to commercial availability.

详细描述

This is a Medical Access Program which will be available to adult patients in the US with metastatic or locally advanced EGFRm NSCLC who have received at least 2 prior systemic therapies, who have no alternative commercially available treatment options, and are not able to enter a clinical trial.

In this Medical Access Program, eligible patients will be treated with HER3-DXd and will continue to receive treatment until any of the following occurs:

  • Disease progression
  • Unacceptable toxicity
  • The benefit-risk no longer favors the individual
  • HER3-DXd becomes commercially available in the US and reimbursement is approved for the concerned indication of the Medical Access Program.
  • Withdrawal of consent
  • Pregnancy
  • Physician discretion
  • Death

研究设计

研究类型
Expanded Access

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

  • 未提供

排除标准

  • 未提供

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (21)

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