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临床试验/EUCTR2015-004068-13-ES
EUCTR2015-004068-13-ES进行中(未招募)1 期

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of PEGylated Recombinant Human Hyaluronidase (PEGPH20) in Combination With nab-Paclitaxel Plus Gemcitabine Compared With Placebo Plus nab-Paclitaxel and Gemcitabine in Subjects with Hyaluronan-High Stage IV Previously Untreated Pancreatic Ductal Adenocarcinoma

Halozyme, Inc.0 个研究点目标入组 420 人开始时间: 2016年3月18日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
420

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

入选标准

  • 1. Signed, written Institutional Review Board/Ethics Committee-approved Informed Consent Form (ICF).
  • 2. Stage IV pancreatic ductal adenocarcinoma (PDA) with histological confirmation of PDA via archived or fresh core biopsy of either the primary tumor or 1 metastatic in minimum of 5-10 unstained core biopsy slides that meet specific tissue sample requirements are required.
  • 3. Subjects must be determined to be HA-high based on tumor biopsy that meets the requirements noted in inclusion criteria #2.
  • 4. If a subject has had adjuvant therapy (chemotherapy for non-metastatic pancreatic cancer in combination with or without radiation therapy), tumor recurrence or disease progression must have occurred no sooner than 6 months after completing the last dose of adjuvant therapy, provided all toxicities have returned to baseline or < = Grade 1.
  • 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 189
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 231

排除标准

  • 1. Clinical evidence of DVT, PE or other known TE event present during the screening period.
  • 2. Previous radiotherapy, surgery, chemotherapy, or investigational therapy for the treatment of metastatic disease.
  • a. Palliative radiotherapy for pain control of metastatic bone lesions is allowed.
  • 3. Known central nervous system involvement or brain metastases.
  • 4. New York Heart Association Class III or IV cardiac disease or myocardial infarction within the past 12 months.
  • 5. History of cerebrovascular accident or transient ischemic attack.
  • 6. Pre-existing carotid artery disease.

研究者

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