跳至主要内容
临床试验/CTIS2022-502982-49-00
CTIS2022-502982-49-00招募中1 期

A Phase 2, Randomized, Open-Label, Study of Lorigerlimab with Docetaxel or Docetaxel Alone in Participants with Metastatic Castration-Resistant Prostate Cancer - CP-MGD019-02

Macrogenics Inc.0 个研究点目标入组 150 人开始时间: 2023年6月2日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
150

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
18 至 65+(—)
性别
Male

入选标准

  • Metastatic castration-resistant adenocarcinoma of the prostate without evidence of neuroendocrine differentiation, signet cell, or small cell features., Participants must have = 1 metastatic (measurable or non-measurable per PCWG3) lesion., Participant has prostate cancer progression at study entry based on PCWG3 criteria., Participant shows evidence of disease progression after receiving at least 1 prior androgen receptor axis-targeted therapy (ARAT) regimen (e.g., abiraterone, enzalutamide, apalutamide, or darolutamide)., Patients with known history of documented breast cancer gene (BRCA) mutation (germline or somatic) must have received an approved poly ADP ribose polymerase (PARP) inhibitor regimen., Participants must have adequate performance status, life expectancy and laboratory values.

排除标准

  • Any condition preventing participant’s ability to receive, tolerate, or comply with the planned treatment or study procedures., Received prior chemotherapy for mCRPC or prior treatment with checkpoint inhibitors for prostate cancer., Current active or chronic infections., Any clinically significant heart, lung, or gastrointestinal disorders., Allergy to any of the study treatments or components of the study treatments.

研究者

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