EUCTR2018-002852-34-BE进行中(未招募)1 期
Progression-free Survival after Minimally Invasive Surgical Microwave Ablation plus Durvalumab (MEDI4736) and Tremelimumab for Unresectable Non-metastatic Locally Advanced Pancreatic Cancer. MIMIPAC trial. - MIMIPAC
ZLeuven0 个研究点目标入组 20 人开始时间: 2019年12月23日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 20
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
- 性别
- All
入选标准
- •Patients with unresectable non-metastatic Locally Advanced Pancreatic Cancer (LAPC) defined according to NCCN guidelines Version 2.2017
- •Histologically proven adenocarcinoma of the pancreas located in the head, body or tail
- •LAPC tumor greatest diameter maximum 5 cm
- •Male or female, age 18 years and older, ECOG PS 0-1
- •Life expectancy of at least 12 weeks
- •Only patients who did not receive chemotherapy for their PC are allowed
- •Patients without distant organ metastases on conventional diagnostic imaging
- •Pre-operative biliary drainage for obstructive jaundice is allowed, but the type of biliary stent is standardized in all jaundiced patients
- •Patients fit for MIS-MWA
- •Able to receive Durvalumab and Tremelimumab.
- •Patients with good liver and renal function and with good hematology
- •Effective contraception for both male and female patients if applicable. Women of childbearing potential must have negative blood pregnancy test at screening visit.
- •Written informed consent (+ optional for TR) must be given according to ICH/GCP and national/European regulations
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 10
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •Metastatic PC on conventional diagnostic imaging or staging laparoscopy
- •LAPC tumor greatest diameter is larger than 5 cm
- •Borderline or resectable PC defined according to the NCCN guidelines version 2.2017
- •Systemic chemo(radio)therapy is not allowed before MIS-MWA
- •Major surgical procedure within 28 days prior to the first dose of investigational products
- •Classic contraindications for PDL and CTLA antibodies
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