Study of Transdermal Testosterone Patches in Menopausal Women With Low Libido

Warner Chilcott

Status and phase

Completed

Phase 3

Conditions

Hypoactive Sexual Desire Disorder

Treatments

Drug: Placebo patch

Drug: Testosterone (transdermal patches)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00131495

2004031 and Yr 2 SB

Details and patient eligibility

About

This study is designed to evaluate the efficacy and safety of 2 doses of the transdermal testosterone patch in naturally or surgically menopausal women with low libido who are not receiving systemic estrogen or estrogen progestin therapy.

Full description

Detailed Description:

Hypoactive sexual desire disorder (HSDD) is a condition suffered by as many as 32% of the menopausal population. It is generally defined as a low libido which causes distress. Testosterone therapy (transdermal patch) is currently under investigation for this disorder and results of three phase 3 trials have shown evidence of efficacy in menopausal patients on hormone replacement therapy. Low libido does not discriminate between those women utilizing hormone replacement therapy and those who do not. This study is designed to evaluate the efficacy and safety of 2 doses of the transdermal testosterone patch in naturally or surgically menopausal women with low libido who are not receiving systemic estrogen or estrogen progestin therapy. Persons could elect to go into a single blind study for one year after completing the first yeat double blind

Enrollment

814 patients

Sex

Female

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Be a generally healthy surgically menopausal woman (12 months), 20 to 70 years of age, not receiving any systemic estrogen or estrogen progestin therapy
Be a generally healthy naturally menopausal woman (2 years since last period), 40 to 70 years of age, not receiving any systemic estrogen or estrogen progestin therapy.
Be, in their own judgment, in a stable monogamous sexual relationship for at least one year prior to study entry that is perceived to be secure and communicative with the same partner who is sexually functional and physically present at least 50% of the time.
Answer affirmatively to ALL of the following questions:
1. Was the patient's sex life before menopause good and satisfying in general?
2. Since menopause, has a meaningful loss in the level of desire for sex occurred?
3. Since menopause, has a significant decrease in sexual activity occurred?
4. Is the current level of desire for or interest in sex bothering or concerning?
5. Is an increase in the level of interest in or desire for sex and sexual activity desired?

Exclusion criteria

Physical limitations that would interfere with normal sexual function;
Estrogen use in the last 12 weeks (vaginal estriol or low dose vaginal estradiol accepted)
Use of any of the following medications:
- antiandrogen therapy or topical minoxidil (last 5 years),
- androgen therapy (past 3 months/implantable past 7 months),
- systemic corticosteroids,
- selective serotonin reuptake inhibitors (SSRIs),
- tricyclic anti-depressants,
- anti-androgens,
- systemic beta-blockers,
- anti-adrenergics,
- spironolactone,
- apomorphine,
- phosphodiesterase type 5 (PDE5) inhibitors (e.g., Viagra, tibolone or selective estrogen receptor modulators (SERMs), including tamoxifen (last 12 weeks))
Be experiencing any chronic or acute life stress relating to any major life change that may significantly interfere with sexual function;
Have significant psychiatric disorder (including mild depressive disorder - Beck Depression Inventory-II score of > 14;
Have current severe dermatological problems or a known suspected hypersensitivity or allergy to any adhesive or any of the constituents of the transdermal testosterone patch
Have evidence of or history of malignancy (estrogen dependent or any gynecological cancer) within the last 5 years;
Have diabetes mellitus, active gallbladder disease, unstable thyroid disease, history of cerebrovascular disease, thrombo-embolic disorders, myocardial infarction or angina within the last 5 years or other significant organic disease that would prevent the patient from completing the study, or otherwise affect the outcome of the study.
Have significant abnormal pretreatment laboratory parameters.