EUCTR2005-005877-31-IT进行中(未招募)不适用
Phase II study Systemic treatment with ZK219477 EPOTHILONE in recurrent Glioblastoma patients - ND
ISTITUTO NEUROLOGICO CARLO BESTA0 个研究点目标入组 15 人开始时间: 2006年4月7日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 15
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
- •- Histologically proven at diagnosis GMB - Age 18-70 years - KPS 70 - Life expectancy of at least 3 months - Presence of at least one bi-dimensionally measurable lesion on gadolinium Gd -enhanced MRI, indicating progressive or recurrent disease at least 8 weeks after standard external-beam radiotherapy - Recurrence or progression after treatment with radiotherapy and temozolomide. Also patients with residual disease after surgery for recurrent GBM will be included - Adequate bone marrow reserve leucocytes 3,500/ml, ANC 1,500, platelets 100,000/ml ; normal baseline liver serum bilirubin 20umol/L , renal serum creatinine 150umol/L and cardiac function - Absence of infectious disease, debilitatig chronic diseases, known psychiatric disorders - Corticosteroid dose stable for at least 1 week - Adequate recovery from previous surgery, radiation and chemotherapy - Negative pregnancy test at enrolment in females of chil-bearing potential - Agreement to use effective contraception methods in adults of reproductive potential - Written informed consent
- •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
- •- Pregnancy - Chemotherapy or radiotherapy within 4 weeks before screening - History of allergic reactions due to compounds of similar chemical or biologic composition to ZK219477 - Uncontrolled intercurrent illness including, but not limited, to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrythmia or psychiatric illness/social situations that would limit compliance with study requirements - HIV infection - Any prior treatment with epothilones, other tubulin-targetting as taxanes e. paclitaxel, docetaxel and vinca alcaloids e.g. vincristine, vinblastine, vinorelbine - Peripheral neuropathy - Any concurrent malignancy other than non-melanoma skin cancer or carcinoma in situ of the cervix - Active infection - Breast-feeding - Subjects who have received an experimental drug or have participated in a clinical trial within 3 months prior to screening - Employees of the investigator or study centre with direct involvement in the proposed study or other studies under the direction of thet investigator or study centre
研究者
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