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临床试验/ISRCTN81721411
ISRCTN81721411已完成2 期

A Phase II, open-label study to evaluate the safety, tolerability, and pharmacokinetic profile of Proxinium™ in patients with recurrent squamous cell carcinoma of the head and neck who have received at least one prior anti-cancer treatment regimen for recurrent disease

Viventia Biotech Inc (Canada)0 个研究点目标入组 18 人开始时间: 2006年8月17日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
18

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

  • 1. The patient must have histologically confirmed SCCHN
  • 2. The patient must have immunohistochemically confirmed Epithelial Cell Adhesion Molecule (Ep-CAM)?positive SCCHN
  • 3. The patient must have received therapy for their primary disease (i.e., SCCHN) consisting of radiotherapy with or without surgery and with or without chemotherapy
  • 4. Patients must have progressed on or after receiving at least one prior anti-cancer treatment regimen containing one or more anti-cancer agents (e.g., chemotherapy, biologic therapy, or photodynamic therapy) for their recurrent disease
  • 5. The patient must have fully recovered or reached a stable state of symptomatology from any previous treatment-related toxicity
  • 6. The patient must have at least one accessible target tumor without direct carotid artery involvement (ie, a distance of less than 5 mm between a tumor and carotid) and must be likely to retain study drug

排除标准

  • 1. The patient has known brain tumor or brain metastases
  • 2. The patient has nasopharyngeal SCCHN
  • 3. The patient has concurrent or documented history of any one of the following:
  • a. Human Immunodeficiency Virus (HIV)
  • b. Hepatitis C virus
  • c. Hepatitis B surface antigen
  • 4. The patient has uncontrolled bleeding from any target tumor(s) that are being considered for Proxinium™ treatment
  • 5. The patient has a history of tumor hemorrhage that has required medical intervention (other than direct compression)
  • 6. The patient is a candidate for surgical tumor resection of their target tumor(s)
  • 7. The patient is pregnant or lactating
  • 8.The patient has clinically significant renal or hepatic disease
  • 9. The patient requires regular use of aspirin, full-dose warfarin, or heparin. Use of low-dose agents to maintain patency of vascular catheters is allowed

研究者

发起方
Viventia Biotech Inc (Canada)

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