跳至主要内容
临床试验/NL-OMON53995
NL-OMON53995招募中不适用

A Phase 1 Study of JNJ-78278343, a T Cell Redirecting Agent Targeting Human Kallikrein 2 (KLK2), for Advanced Prostate Cancer - 78278343PCR1001

Janssen-Cilag0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
Janssen-Cilag
入组人数
25

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 99(—)

入选标准

  • Each potential participant must satisfy all of the following criteria to be
  • enrolled in the study:
  • 1. 18 years of age or older.
  • Disease Characteristics
  • 2. Confirmed adenocarcinoma of the prostate which has spread to other body
  • 3. Measurable or evaluable disease
  • 4. Prior treatment with at least 1 prior novel androgen receptor (AR)-targeted
  • therapy or chemotherapy.
  • 5. Prior surgical removal of testicles; or, for participants who have not
  • undergone surgical removal of testicles, must be receiving ongoing androgen
  • deprivation therapy (ADT) with a gonadotropin releasing hormone analog.
  • 6. Concurrent use of any other anticancer treatment.
  • 7. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

排除标准

  • Any potential participant who meets any of the following criteria will be
  • excluded from participating in the study:
  • Disease Conditions
  • 1. Active central nervous system (CNS) involvement.
  • 2. Toxicity related to prior anticancer therapy has not adequately recovered.
  • Prior/Concomitant Therapy
  • 3. Prior treatment with KLK2-targeted therapy.
  • 4. Received, or are receiving, medications that suppress the immune system
  • within 3 days prior to the first dose of study drug.
  • 5. Received or plans to receive any live, attenuated vaccine within 4 weeks
  • prior to the first dose of study drug.
  • Prior/Concurrent Medical Conditions
  • 6. Diagnosis of cancer other than prostate cancer within 2 years prior to the
  • first dose of study drug.
  • 7. Solid organ or bone marrow transplantation.
  • 8. Major clotting diseases within one month prior to the first dose of study
  • 9. Active autoimmune disease within 12 months prior to the first dose of study
  • 10. Active infection.
  • 11. Major diseases of heart and blood vessels within 6 months prior to the
  • first dose of study drug.
  • 12. Clinically significant lung diseases.
  • 13. Active or chronic hepatitis B or hepatitis C infection.
  • 14. Known positive test result for human immunodeficiency virus (unless stable
  • on antiretroviral therapy with undetectable viral load).
  • 16. Any serious underlying medical conditions or other issue that would impair
  • the ability of the participant to receive or tolerate the planned treatment.

研究者

发起方
Janssen-Cilag

相似试验