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临床试验/EUCTR2020-005767-31-ES
EUCTR2020-005767-31-ES进行中(未招募)1 期

A Phase 1b/2, Randomized, Controlled, Open-Label Study Evaluating the Safety and Efficacy of ABBV-927 Administered in Combination with Modified FOLFIRINOX (mFFX) With or Without Budigalimab compared to mFFX in Subjects with Untreated Metastatic Pancreatic Adenocarcinoma

AbbVie Deutschland GmbH & Co. KG0 个研究点目标入组 129 人开始时间: 2021年6月23日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
129

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1) Histologically or cytologically confirmed diagnosis of pancreatic adenocarcinoma with metastatic disease
  • 2) Measurable disease per RECIST 1.1
  • 3) ECOG 0 or 1 and life expectancy of > 3 months
  • 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 97
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 32

排除标准

  • 1) Previous radiotherapy, surgery, or systemic anti-cancer therapy for the treatment of metastatic pancreatic adenocarcinoma
  • 2) Clinically significant third-space fluid accumulation
  • 3) History of inflammatory bowel disease, non-infectious pneumonitis, interstitial lung disease, Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), or drug reaction with eosinophilia and systemic symptoms (DRESS)
  • 4) Positive test results for HIV, or subjects with chronic or active hepatitis B or C
  • 5) Clinically significant uncontrolled medical conditions

研究者

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