跳至主要内容
临床试验/CTRI/2021/11/038126
CTRI/2021/11/038126已完成未知

A Multi-country, Multi-centre, Non-interventional, REtrospective Study to Describe the Real-world Treatment Patterns and Associated Clinical Outcomes in Patients With Metastatic Castration-resistant PROstate Cancer - REMPRO Registry

AstraZeneca Pharma India Ltd0 个研究点目标入组 200 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • 1. Male patients = 18 years of age OR legal age of being an adult in the country as per local
  • regulations
  • 2. Patient or next of kin/legal representative (for deceased patients at study entry, unless a
  • waiver is granted) willing and able to provide written informed consent according to the
  • local regulations
  • 3. Patients with a diagnosis of metastatic (stage IV) mCRPC, confirmed by either biopsy of a
  • metastatic tumour site, or by history of biopsy-proven localized disease and evidence of
  • metastatic disease on imaging studies (which is clearly noted in hospital/clinical records)
  • and progression on ADT alone between 01 January 2016 and 31 December 2018
  • 4. Availability of medical records at the participating site reflecting at least one LOT
  • received and at least 12 months of follow-up from the index date (unless the patient
  • died/lost to follow-up within the first 12 months after diagnosis)

排除标准

  • 1. Patients with a concomitant cancer at the time of diagnosis of mCRPC or those who are
  • treated with any anti-cancer therapy indicated for other cancers within 6 months of
  • diagnosis of mCRPC, except for non-metastatic non-melanoma skin cancers or in situ or
  • benign neoplasms.
  • 2. Patients unable to give an informed consent (unless a waiver is granted)

研究者

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