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临床试验/CTIS2024-511125-61-00
CTIS2024-511125-61-00招募中1 期

An open-label, multi-center rollover protocol for patients who have participated in a Novartis-sponsored ribociclib (LEE011) study and are continuing to benefit from ribociclib as single agent or in combination with other investigational treatments - CLEE011X2X01B

ovartis Pharma AG0 个研究点目标入组 4 人开始时间: 2024年4月11日最近更新:

试验速览

阶段
1 期
状态
招募中
入组人数
4

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 65+(—)
性别
All

入选标准

  • Patient is currently enrolled in an eligible Novartis-sponsored ribociclib (LEE011) study and is receiving ribociclib as single agent or in combination with other investigational treatments., Patient is currently deriving clinical benefit from the study treatment, as determined by the investigator., Patient has demonstrated compliance, as assessed by the investigator, with the parent protocol requirements.

排除标准

  • Patients who have permanently discontinued from ribociclib (LEE011) in the parent protocol for any reason, Patients who do not meet parent protocol criteria to continue study treatment.

研究者

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