Phase II randomized trial of the Polo-like kinase 1 inhibitor BI 6727monotherapy versus investigator’s choice chemotherapy in ovariancancer patients resistant or refractory to platinum-based cytotoxictherapy - BI 6727 randomised phase II trial in ovarian cancer

Boehringer Ingelheim AB0 个研究点目标入组 118 人开始时间: 2010年4月14日最近更新: 2015年7月10日

研究概览

暂无简介。

•- Females, age = 18 years
•- Confirmed epithelial ovarian cancer, peritoneal carcinoma or fallopian tube cancer
•- Platinum-resistant disease (disease progression within a platinum-free interval of = 6 months after the final dose of primary or subsequent platinum-based therapy) or platinum-refractory disease (disease progression during primary or subsequent platinum-based therapy. Stable disease as best response to primary or subsequent Platinum-based therapy )
•- The patient has completed at least two and up to three chemotherapy regimens for the management of this condition, one of which may have been treatment for platinum resistant or refractory disease. Treatment may have included intraperitoneal therapy, consolidation or extended therapy after surgical or non surgical assessment.
•- ECOG performance status = 2
•- Life expectancy = 3 months
•- At least, one measurable or non-measurable lesion according to RECIST 1.1
•- Adequate hepatic, renal and bone marrow functions
•- Signed and dated written informed consent prior to admission to the study
•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

•- Contre-indications for cytotoxic treatment according to the SPC (Arm B)
•- Clinical evidence of active brain metastasis or leptomeningeal involvement
•- Other malignancy currently requiring active therapy
•- QTcF prolongation deemed clinically relevant by the investigator (e.g., congenital long QT syndrome, QTcF > 470ms etc.)
•- Hypersensitivity to one of the trial drugs or the excipients
•- Serious illness or concomitant non-oncological disease
•- Systemic anticancer therapy within 4 weeks before the start of the study.

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