跳至主要内容
临床试验/2025-521621-33-00
2025-521621-33-00招募中4 期

Long-term Safety Outcomes in Patients Treated With Replimune Oncolytic Immunotherapy Products

Replimune Group Inc.3 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2026年2月9日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
13
试验地点
3
主要终点
Evaluation of delayed adverse event(s) will be based on the occurrence of: New malignancy(ies); New incidence or exacerbation of a pre-existing neurologic disorder​; New incidence or exacerbation of a pre-existing rheumatologic or other autoimmune disorder; New incidence of a hematologic disorder; New incidence of infection related to RPx​

研究概览

简要总结

To evaluate the long-term safety of patients treated with an RPx product and identify any delayed adverse event(s) related to treatment with an RPx product

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Patient has received at least 1 dose of an RPx product and has completed or discontinued participation in the parent study.
  • Patient or patient’s legal guardian has provided signed informed consent (or assent), which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

排除标准

  • Cannot comply with the requirements of the study.

结局指标

主要结局

Evaluation of delayed adverse event(s) will be based on the occurrence of: New malignancy(ies); New incidence or exacerbation of a pre-existing neurologic disorder​; New incidence or exacerbation of a pre-existing rheumatologic or other autoimmune disorder; New incidence of a hematologic disorder; New incidence of infection related to RPx​

Evaluation of delayed adverse event(s) will be based on the occurrence of: New malignancy(ies); New incidence or exacerbation of a pre-existing neurologic disorder​; New incidence or exacerbation of a pre-existing rheumatologic or other autoimmune disorder; New incidence of a hematologic disorder; New incidence of infection related to RPx​

New herpetic infection and presence of RPx detected in samples collected from herpetic lesions

New herpetic infection and presence of RPx detected in samples collected from herpetic lesions

次要结局

未报告次要终点

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Kari Jeschke

Scientific

Replimune Group Inc.

研究点 (3)

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