A Study to Evaluate the Safety and Effectiveness of Three Asoprisnil Doses in the Treatment of Women With Endometriosis

Phase 2

Completed

• Conditions: Endometriosis
• Interventions: Drug: Asoprisnil; Drug: Placebo

• Registration Number: NCT00160446
• Lead Sponsor: Abbott

Brief Summary

The objective of this study is to determine the safety and effectiveness of three doses of asoprisnil, compared to placebo, in the treatment of women with endometriosis.

Detailed Description

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 safety and efficacy of asoprisnil 5, 10, and 25 mg tablets, compared to placebo, administered daily for 12 weeks to women with endometriosis, by assessing whether asoprisnil administration diminishes the pelvic pain, dysmenorrhea, dyspareunia, excessive bleeding, and analgesic use associated with this disease and lessens the subjects' perceived pain symptoms. Otherwise healthy women with surgically confirmed endometriosis will be enrolled.

Study Timeline

• Study Start: 2000-05
• Primary Completion: 2001-07
• Study Completion: 2001-07
• Study First Submitted: 2005-09-08
• Study First Submitted QC: 2005-09-08
• Study First Posted: 2005-09-12
• Status Verified: 2008-05
• Last Update Submitted: 2008-05-27
• Last Update Posted: 2008-05-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 130

Inclusion Criteria

• Surgically confirmed endometriosis

• History of menstrual cycles between 26 and 32 days

• Otherwise in good health

• Age 18-40 years, inclusive

• Subject had pain graded at Screening and Day 1 according to a scale suggested by Biberoglu and Berhman5 in at least one of the following categories:

  1. moderate or severe pelvic pain not related to menstruation, OR
  2. moderate or severe dysmenorrhea, OR
  3. moderate or severe pelvic tenderness elicited on pelvic examination accompanied by non-menstrual pelvic pain.

• Subject agrees to double barrier method of contraception

Exclusion Criteria

• Any abnormal lab or procedure result the study-doctor considers important
• History of undiagnosed uterine bleeding or gynecological disorder
• Severe reaction(s) to hormone therapy
• History of osteoporosis or other metabolic bone disease
• Subject currently breast feeding

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
2	Asoprisnil	-
3	Asoprisnil	-
4	Placebo	-
1	Asoprisnil	-

Primary Outcome Measures

Name	Time	Method
Pain (dysmenorrhea, dyspareunia, pelvic pain) measured by daily diary	Mean change from baseline to Months 1, 2, 3

Secondary Outcome Measures

Name	Time	Method
Global efficacy question	Final visit
Pain (dysmenorrhea, dyspareunia, pelvic pain) pelvic tenderness and induration evaluated during office visits using modified Biberoglu and Behrman grading scale	Each monthly visit