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临床试验/NCT06877676
NCT06877676Approved For Marketing不适用

Pre-Approval Access US Intermediate Size Expanded Access Protocol for TAR-200 Treating Physician Use

Janssen Research & Development, LLC0 个研究点开始时间: 2025年3月14日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
Approved For Marketing

研究概览

简要总结

The purpose of this pre-approval access program is to provide access to TAR-200 prior to its marketing authorization for the treatment of participant(s) with high-risk non-muscle invasive bladder cancer (HR-NMIBC).

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
否

入选标准

  • •Participant has exhausted all clinically appropriate alternative forms of treatment and is not eligible for, or does not have access to, a clinical trial
  • •Histologically confirmed diagnosis of persistent or recurrent high-risk non-muscle-invasive bladder cancer (HR-NMIBC), carcinoma in situ (CIS) (OR Tis) with or without papillary disease (T1, high-grade Ta), within 12 months of completion of the last dose of BCG therapy, in participants who have received adequate Bacillus Calmette-Guérin (BCG)
  • •All visible papillary disease must be fully resected (absent) prior to initiation of treatment
  • •Participants must be ineligible for or have elected not to undergo Radical Cystectomy (RC)
  • •Have an Eastern Cooperative Oncology Group (ECOG) performance status Grade of 0, 1, or 2

排除标准

  • •Presence or history of histologically confirmed, muscle invasive, locally advanced, nonresectable, or metastatic urothelial carcinoma (that is, T2, T3, T4, and/or Stage IV)
  • •Presence of any bladder or urethral anatomic feature that, in the opinion of the Investigator, may prevent the safe placement, indwelling use, or removal of TAR-
  • •Participants with tumors involving the prostatic urethra in men will be excluded
  • •Evidence of bladder perforation during diagnostic cystoscopy
  • •A history of clinically significant polyuria with recorded 24-hour urine volumes greater than 4000 milliliters (>4000 mL)
  • •Active malignancies (i.e., progressing or requiring treatment change in the last 24 months) other than HR-NMIBC

研究者

申办方类型
Industry
责任方
Sponsor

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