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临床试验/NCT07632690
NCT07632690尚未招募3 期

A Randomized, Open-label, Controlled, Multicenter Phase III Clinical Trial Comparing QLC5508 Versus Docetaxel in Participants With Metastatic Castration-resistant Prostate Cancer (mCRPC) Who Have Progressed After Treatment With Novel Hormonal Agents (NHA).

Qilu Pharmaceutical Co., Ltd.0 个研究点目标入组 700 人开始时间: 2026年6月20日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
700

研究概览

简要总结

This is a randomized, open-label, active-controlled, multicenter Phase III trial evaluating QLC5508 versus docetaxel in participants with metastatic castration-resistant prostate cancer (mCRPC) who have progressed after prior treatment with novel hormonal agents (NHAs). Participants are randomized to receive either QLC5508 monotherapy (experimental arm) or docetaxel (control arm). The primary objective is to compare the efficacy of QLC5508 versus docetaxel, as measured by radiographic progression-free survival (rPFS) assessed by an Independent Radiological Review Committee (IRC).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Male, aged ≥18 years.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or
  • Life expectancy of at least 3 months.
  • Histologically or cytologically confirmed adenocarcinoma of the prostate without evidence of small-cell features.
  • Diagnosis of metastatic castration-resistant prostate cancer (mCRPC).
  • Prior treatment with novel hormonal agents (NHAs) and documented disease progression.
  • Adequate organ function.
  • Recovery from all reversible adverse events (AEs) related to prior anticancer therapies.

排除标准

  • 1. Prior treatment with a B7-H3-targeted therapy, or with an antibody-drug conjugate (ADC) using a topoisomerase I inhibitor (TOP1i) as the payload, or with any TOP1i-class agent.
  • 2. History of or current significant cardiovascular or cerebrovascular disease.
  • Active, uncontrolled infection.
  • Concurrent or prior history of another primary malignancy
  • History of interstitial lung disease (ILD) or non-infectious pneumonitis, or current ILD/non-infectious pneumonitis
  • Current hepatic encephalopathy, hepatorenal syndrome, or cirrhosis classified as Child-Pugh class B or worse.
  • 7. Known hypersensitivity or allergy to any investigational product or its excipients.

研究者

申办方类型
Industry
责任方
Sponsor

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