跳至主要内容
临床试验/NCT00569257
NCT00569257已完成2 期

Antitumoral Activity and Safety of AEZS-108 (AN-152), a LHRH Agonist Linked Doxorubicin, in Women With LHRH Receptor Positive Gynecological Tumors

AEterna Zentaris34 个研究点 分布在 2 个国家目标入组 85 人开始时间: 2007年12月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
85
试验地点
34
主要终点
Tumor response as per RECIST or (for Ovarian CA patients without evaluable target lesion following RECIST) GCIG criteria

研究概览

简要总结

The purpose of this study is to determine whether AEZS-108 shows anti-tumor activity and is tolerated in patients with gynecological tumors (ovarian / endometrial cancer) that have been shown to express receptors for the luteinizing hormone releasing hormone (LHRH)

详细描述

The ovary and the endometrium are hormone dependent organs. Receptors for different sex hormones are found commonly in epithelial ovarian and endometrial cancers. LHRH and its receptors are expressed in about 80% of human ovarian and endometrial cancers. As binding sites are present on tumors in higher concentrations than on most normal tissues, these receptors represent a specific target for AEZS-108 in which doxorubicin is coupled to an LHRH analog.

Patients whose tumor specimen have shown to be positive for LHRH receptor expression will be investigated for tumor response and tolerability.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • LHRH receptor positive tumor status: positive receptor status determined by immunohistochemistry from primary tumor
  • Histologically confirmed epithelial ovarian cancer (Stratum A)
  • Advanced (FIGO III or IV) or recurrent disease
  • Progression during treatment with a platinum-based regimen or within 6 months after receiving a platinum-based regimen
  • Previous treatment with a taxane-containing regimen
  • At least one measurable target lesion (RECIST criteria) OR CA125 level higher than twice the upper limit of normal range (GCIG criteria)
  • Histologically confirmed endometrial cancer (Stratum B)
  • Advanced (FIGO III or IV) or recurrent disease not amenable to potentially curative treatment with local surgery and/or radiation therapy
  • No previous anthracycline-based chemotherapy
  • At least one measurable target lesion according to RECIST criteria

排除标准

  • 未提供

结局指标

主要结局

Tumor response as per RECIST or (for Ovarian CA patients without evaluable target lesion following RECIST) GCIG criteria

时间窗: up to six 3-weekly treatment cycles

次要结局

  • Time-to-progression (TTP); Overall survival(up to observation of event)
  • Safety of AEZS-108 (possibly drug-related adverse events)(4 weeks beyond last drug admnistration)

研究者

发起方
AEterna Zentaris
申办方类型
Industry
责任方
Sponsor

研究点 (34)

Loading locations...

相似试验

进行中(未招募)
不适用
Antitumoral activity and safety of AEZS-108 (AN-152), a LHRH agonist linked doxorubicin, in women with LHRH receptor positive gynecological tumors - AEZS-108 in patients with LHRH receptor positive gynecological tumorsHistologically confirmed malignancy of ovary or endometrium that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective andLHRH receptor positive tumor statuspositive receptor status determined by immunohistochemistry from primary tumorMedDRA version: 9.1Level: LLTClassification code 10007069Term: Cancer of endometrium stage IIIMedDRA version: 9.1Level: LLTClassification code 10007065Term: Cancer of endometrium recurrentMedDRA version: 9.1Level: LLTClassification code 10007070Term: Cancer of endometrium stage IVMedDRA version: 9.1Level: LLTClassification code 10057529Term: Ovarian cancer metastaticMedDRA version: 9.1Level: PTClassification code 10066697Term: Ovarian cancer recurrent
EUCTR2007-002663-26-DEAEterna Zentaris GmbH82
进行中(未招募)
不适用
Antitumoral activity and safety of AEZS-108 (AN-152), a LHRH agonist linked doxorubicin, in women with LHRH receptor positive gynecological tumors - AEZS-108 in patients with LHRH receptor positive gynecological tumors
EUCTR2007-002663-26-BGAEterna Zentaris GmbH82
终止
1 期
A Phase I/II Trial of AEZS-108 in Urothelial Cancer Patients Who Failed Platinum-chemotherapyUrothelial Carcinoma
NCT01234519AEterna Zentaris12
终止
2 期
Phase 2 Trial of AEZS-108 in Chemotherapy Refractory in Triple Negative Breast CancerBreast Cancer
NCT01698281AEterna Zentaris7
进行中(未招募)
不适用
Trial with AEZS-108 in a special type of breast tumor
EUCTR2012-000134-19-DEAeterna Zentaris GmbH74