EUCTR2006-001358-29-DE进行中(未招募)不适用
A Phase 2 Study of ARQ 501 in Combination with Gemcitabine in Adult Patients with Treatment Naive, Unresectable Pancreatic Adenocarcinoma
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- ARQule Inc.
- 入组人数
- 75
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. Able to provide signed and dated informed consent prior to study-specific
- •screening procedures.
- •2. Have a pathologically confirmed diagnosis of unresectable pancreatic adenocarcinoma.
- •3. Measurable disease per RECIST.
- •4. greater or equal 18 years old.
- •5. Karnofsky Performance Status (KPS) of greater or equal 70%.
- •6. Male or female patients of child-producing potential must agree to use contraception or avoidance of pregnancy measures during the study and for 30 days after the last infusion of ARQ 501.
- •7. Hemoglobin (Hgb) greater or equal 10 g/dL.
- •8. Absolute neutrophil count (ANC) greater or equal 1.5 × 109/L (greater or equal 1,500/mm3).
- •9. Platelet count greater or equal 100 × 109/L (greater or equal 100,000/mm3).
- •10. Total bilirubin lower or equal 1.5 × upper limit of normal (ULN) or lower or equal 3.0 × ULN with metastatic liver disease.
- •11. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) lower or equal 2.5 × ULN or lower or equal 5.0 × ULN with metastatic liver disease.
- •12. Creatinine lower or equal 1.5 × ULN.
- •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
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Received any prior therapy for the treatment of their pancreatic malignancy (including chemotherapy, immunotherapy, vaccines, monoclonal antibodies, major surgery, or irradiation, whether conventional or investigational).
- •2. Have an active, uncontrolled systemic infection considered opportunistic, life threatening or clinically significant at the time of treatment.
- •3. Are pregnant or lactating.
- •4. Have a psychiatric disorder(s) that would interfere with consent, study participation, or follow-up.
- •5. Symptomatic or untreated central nervous system (CNS) metastases.
研究者
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ARQ 501 in Combination With Gemcitabine in Subjects With Pancreatic CancerAdenocarcinomaPancreatic CancerNCT00102700ArQule, Inc., a subsidiary of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc. (Rahway, NJ USA)66
