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临床试验/NCT00160420
NCT00160420已完成2 期

A Phase 2, 12-Month, Open Label Extension Study to Evaluate the Safety of J867(5 mg QD) in Subjects With Endometriosis

Abbott0 个研究点目标入组 73 人开始时间: 2002年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Abbott
入组人数
73
主要终点
Change from baseline in pelvic pain and dysmenorrhea assessed by visual analog scale.

研究概览

简要总结

The objective of this study is to determine the long-term safety of asoprisnil 5 mg for 12 months in women with endometriosis from study M01-398.

详细描述

Endometriosis, the presence of endometrial tissue outside the uterus, is a progressive, estrogen-dependent disease that occurs in menstruating women of reproductive age. Although all major endometriosis therapies are effective for the treatment of pain, no single treatment is superior to others in terms of efficacy. The major drawbacks of the current medical therapies are severe side effects such as hot flushes and osteoporosis. The objective of this study is to determine the long-term safety of asoprisnil 5 mg daily for 12 months in women with endometriosis, after an initial 12 weeks in study M01-398. The safety will be based on assessments of the endometrium, lipid profiles, adverse events, and changes from baseline laboratory values and vital signs.

研究设计

研究类型
Interventional
分配方式
Non Randomized
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 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Completed 3 months of dosing and Month 3 procedures in study M01-398
  • Otherwise in good health
  • Month 3 (M01-398) ultrasound reveals no significant gynecologic disorder

排除标准

  • Any abnormal lab or procedure result the study-doctor considers important
  • Anticipated need for excluded hormonal therapy or unapproved narcotics

研究组 & 干预措施

1

Experimental

干预措施: Asoprisnil (Drug)

结局指标

主要结局

Change from baseline in pelvic pain and dysmenorrhea assessed by visual analog scale.

时间窗: Months 1,3,6,9,12 and final visit

Change from baseline in pelvic pain, dysmenorrhea, dyspareunia, pelvic tenderness and induration assessed by modified Biberoglu and Behrman grading scale.

时间窗: Months 3,6,9,12 and final visit

次要结局

  • Percentage of subjects with amenorrhea.(Throught treatment period.)

研究者

发起方
Abbott
申办方类型
Industry

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