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临床试验/RPCEC00000054
RPCEC00000054已完成2 期

Clinical trial, phase II: Evaluation of TheraCIM hR3 MaB combined with chemo- and radio-therapy to treat patients with epithelial tumors in neck of the uterus, stage III.

Center of Molecular Inmununology(CIM)0 个研究点目标入组 148 人开始时间: 2010年12月27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
148

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled trial. Masking: Single Blind. Control group: Placebo. Assignment: Parallel. Purpose: Treatment

入排标准

年龄范围
18 years 至 70 years(—)
性别
Female

入选标准

  • 1) Patients giving their consent in writing to participate in the trial. 2) Female patients with measurable lesions, defined as those that can be exactly measured in one dimension at least (greater diameter) and have a diameter equal to or higher than 20mm, using conventional techniques (abdominal CAT, X rays, US), or higher than or equal to 10mm, using spiral CAT or clinical tests. 3) Patients aged 18 to 70. 4) General condition under ECOG =2. 5) Patients whose organs and bone marrow are working normally, as defined by the following parameters: - Hemoglobin >= 10g/L - Leucocytes >= 4,000/mL- Absolute neutrophil count >= 1,500/mL – Platelet count >= 100,000/L – Total bilirubin: up to 1.5 times the normal value - Total proteins: Within normal limits - TGP and TGO <= 2.5 times the institutional higher normal value – Serum creatinine: Within normal limits, and glomerular filtering based on Cockcrof Formula – Creatinine clearing = (140-age) x weight (kg)/72 x serum creatinine. Following clinical criteria, glomerular filtering will be performed only on patients whose kidney function is thought to be affected. (Normal laboratory values will be in keeping with the technology and equipment available where tests are conducted). 6) Female patients will be included in the study.

排除标准

  • 1. Pregnancy or breastfeeding. 2. Patients on another onco-specific drug under research (except EPOCIM and/or LeukoCIM). 3. Patients with history of allergy to chemical and biological compounds similar to the monoclonal antibody under evaluation. 4. Patients with uncontrolled intercurrent diseases, including active infections, symptomatic congestive cardiac failure, unstable angina pectoris, cardiac arrhythmia, uncontrolled diabetes, and psychiatric diseases. 5. Presence of a second tumor, except patients who have been on appropriate treatment for skin (basal or scaly) carcinomas.

研究者

发起方
Center of Molecular Inmununology(CIM)

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