Uptitration Trial of Flibanserin Versus Placebo in Premenopausal Women With Hypoactive Sexual Desire Disorder

NCT00360555 | Completed Phase 3 Results DMC

• 1 other identifier: 511.75
• Study Type: interventional
• Target: 1,584
• Locations: 2 countries
• Sites: 77

Brief Summary

This trial is designed to assess the safety and efficacy of flibanserin in the treatment of premenopausal women with Hypoactive Sexual Desire Disorder (HSDD) that meets standard diagnostic criteria. Efficacy for flibanserin will be assessed vs. a parallel placebo group.

Conditions

Sexual Dysfunctions, Psychological

Outcome Measures

Primary Outcomes (2)

• Change From Baseline in the Frequency of Satisfying Sexual Events (SSE) as Recorded in the eDiary.

  For endpoints collected on the eDiary, responses are accumulated on a monthly basis using the following algorithms. For satisfying sexual events: Total monthly events = 28 x (sum of the number of events) / (sum of number of days entered)

  baseline to 28 weeks

• Change From Baseline in the Monthly Sum of Responses Recorded in the eDiary to the Daily Desire Question.

  Change from baseline in the electronic diary (eDiary) Sexual Desire Monthly Total Score standardized to a 28-day period (score range 0-84). Change from baseline is calculated as the difference between the four week baseline period and Week 21 to Week 24. Patients were asked to record information daily in the eDiary throughout the trial. Every time the eDiary was completed, a desire question was asked. If a patient did not complete the diary on a given day, the patient was not asked to enter desire information for more than a 24-hour retrospective period. The desire item read "Indicate your most intense level of sexual desire in the last 24 hours / since your last visit." Potential responses included "no," "low," "moderate," or "strong" and was scored 0-3, with 0 indicating no desire and 3 indicating the highest level of desire: 0 = No desire 1. = Low desire 2. = Moderate desire 3. = Strong desire

  baseline to 24 weeks

Study Arms (4)

flibanserin

EXPERIMENTAL

flibanserin 25 mg b.i.d

Drug: flibanserin 50mg

flibanserin 50mg

EXPERIMENTAL

flibanserin 50mg qhs/b.i.d

Drug: flibanserin 100mg

flibanserin 100mg

EXPERIMENTAL

flibanserin 50mg b.i.d./100mg qhs

Drug: placebo

placebo

PLACEBO COMPARATOR

placebo comparator

Drug: flibanserin

Interventions

flibanserin DRUG

flibanserin 25 mg b.i.d

placebo

flibanserin 50mg DRUG

flibanserin 50mg qhs/b.i.d.

flibanserin

flibanserin 100mg DRUG

flibanserin 50 mg b.i.d/100mg qhs

flibanserin 50mg

placebo DRUG

placebo comparator

flibanserin 100mg

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Women who are 18 years of age and older.
• Premenopausal women having regular menstrual periods who have HSDD (decreased sexual desire), generalized acquired type, according to DSM IV-TR criteria.
• Patient must meet minimum cut-off scores on questionnaires relating to sexual functioning and sexual distress.
• Patients must be willing to try to have sexual activity (e.g., any act involving direct genital stimulation) at least once monthly.
• Patients must be willing and able to use an electronic diary on a daily basis (e.g., have access to a working land line telephone for daily data transmissions).
• At the Baseline Visit, patients must have complied with eDiary use adequately.
• Patients must be in a stable, monogamous, heterosexual relationship that is secure and communicative, for at least 1 year prior to the Screen Visit. The partner is expected to be physically present at least 50% of each month.
• Patients must have used a medically acceptable method of contraception for at least 3 months before the Baseline Visit (Visit 2) and continue to use that medically acceptable method of contraception during the trial.
• In the investigators opinion, patients must be reliable, honest, compliant, and agree to co-operate with all trial evaluations as well as to be able to perform them.
• Patients must be able and willing to give meaningful, written informed consent prior to participation in the trial, in accordance with regulatory requirements. Patients must have sufficient understanding to communicate effectively with the investigator, and be willing to discuss their sexual functioning with the investigative staff.
• Patients must have a clinically acceptable Pap smear as read by a cytology facility (no evidence of malignancy or squamous intraepithelial lesions) within 6 months before the Screen Visit.
• A score of 15 or higher on the FSDS-R at the screen Visit.

You may not qualify if:

• Patients who have taken any medication noted in the protocols List of Prohibited Medications within 30 days before screening.
• Patients whose sexual function was affected (enhanced or worsened) in the investigators opinion by any medication within 30 days before the Screen Visit and anytime prior to the Baseline Visit.
• Patients with a history of drug dependence or abuse within the past one year.
• Patients with a history of multiple severe reactions (i.e., allergic or oversensitivity to usual doses) to drugs that affect the brain.
• Patients with a history of participation in a trial of another investigational medication within one month prior to the Screen Visit, or participation in any previous clinical trial of flibanserin.
• Patients who meet accepted diagnostic criteria for sexual disorders that would interfere with improvement in HSDD (sexual aversion, substance-induced sexual problems, urge to live as a man, etc.
• Patients who indicate that their sexual partner has inadequately treated sexual problems that could interfere with the patients response to treatment.
• Patients who have entered the menopausal transition or menopause or have had a hysterectomy.
• Patients with findings at the Screen Visit of infection, inflammation, undue tenderness, or shrinkage (atrophy) of the female organs.
• Patients who are breast feeding or have breastfed within the last 6 months prior to the Baseline Visit.
• Patients who are pregnant or have been pregnant within the last 6 months prior to the Baseline Visit.
• Patients with a history of Major Depressive Disorder within 6 months prior the Screen Visit, a score indicating depression on a depression scale, a history of suicide attempt, or current suicidal ideation evident at the Screen or Baseline Visit.
• Patients with a history of any other psychiatric disorders that could impact sexual function, risks patients safety, or may impact compliance.
• Patients who have started psychotherapy

Sponsors & Collaborators

• Sprout Pharmaceuticals, Inc: lead

Study Sites (77)

511.75.01015 Boehringer Ingelheim Investigational Site

Birmingham, Alabama, United States

Location

511.75.01028 Boehringer Ingelheim Investigational Site

Mobile, Alabama, United States

Location

511.75.01051 Boehringer Ingelheim Investigational Site

Phoenix, Arizona, United States

Location

511.75.01063 Boehringer Ingelheim Investigational Site

Little Rock, Arkansas, United States

Location

511.75.01017 Boehringer Ingelheim Investigational Site

Berkeley, California, United States

Location

511.75.01014 Boehringer Ingelheim Investigational Site

Encinitas, California, United States

Location

511.75.01042 Boehringer Ingelheim Investigational Site

Fair Oaks, California, United States

Location

511.75.01022 Boehringer Ingelheim Investigational Site

Irvine, California, United States

Location

511.75.01005 Boehringer Ingelheim Investigational Site

La Jolla, California, United States

Location

511.75.01053 Boehringer Ingelheim Investigational Site

Sacremento, California, United States

Location

511.75.01045 Boehringer Ingelheim Investigational Site

San Diego, California, United States

Location

511.75.01065 Boehringer Ingelheim Investigational Site

Aurora, Colorado, United States

Location

511.75.01003 Boehringer Ingelheim Investigational Site

Englewood, Colorado, United States

Location

511.75.01030 Boehringer Ingelheim Investigational Site

Washington D.C., District of Columbia, United States

Location

511.75.01066 Boehringer Ingelheim Investigational Site

Coral Gables, Florida, United States

Location

511.75.01040 Boehringer Ingelheim Investigational Site

Fort Meyers, Florida, United States

Location

511.75.01001 Boehringer Ingelheim Investigational Site

Gainesville, Florida, United States

Location

511.75.01062 Boehringer Ingelheim Investigational Site

Hollywood, Florida, United States

Location

511.75.01032 Boehringer Ingelheim Investigational Site

Ocala, Florida, United States

Location

511.75.01047 Boehringer Ingelheim Investigational Site

Orlando, Florida, United States

Location

511.75.01073 Boehringer Ingelheim Investigational Site

Palm Bay, Florida, United States

Location

511.75.01035 Boehringer Ingelheim Investigational Site

Sarasota, Florida, United States

Location

511.75.01010 Boehringer Ingelheim Investigational Site

South Miami, Florida, United States

Location

511.75.01041 Boehringer Ingelheim Investigational Site

St. Petersburg, Florida, United States

Location

511.75.01033 Boehringer Ingelheim Investigational Site

Tampa, Florida, United States

Location

511.75.01002 Boehringer Ingelheim Investigational Site

West Palm Beach, Florida, United States

Location

511.75.01006 Boehringer Ingelheim Investigational Site

Sandy Springs, Georgia, United States

Location

511.75.01023 Boehringer Ingelheim Investigational Site

Chicago, Illinois, United States

Location

511.75.01031 Boehringer Ingelheim Investigational Site

Fort Wayne, Indiana, United States

Location

511.75.01050 Boehringer Ingelheim Investigational Site

Lafayette, Louisiana, United States

Location

511.75.01043 Boehringer Ingelheim Investigational Site

Bingham Farms, Michigan, United States

Location

511.75.01025 Boehringer Ingelheim Investigational Site

Chaska, Minnesota, United States

Location

511.75.01024 Boehringer Ingelheim Investigational Site

Chesterfield, Missouri, United States

Location

511.75.01009 Boehringer Ingelheim Investigational Site

Kansas City, Missouri, United States

Location

511.75.01060 Boehringer Ingelheim Investigational Site

Las Vegas, Nevada, United States

Location

511.75.01004 Boehringer Ingelheim Investigational Site

New Brunswick, New Jersey, United States

Location

511.75.01037 Boehringer Ingelheim Investigational Site

Chapel Hill, North Carolina, United States

Location

511.75.01054 Boehringer Ingelheim Investigational Site

Winston-Salem, North Carolina, United States

Location

511.75.01069 Boehringer Ingelheim Investigational Site

Beachwood, Ohio, United States

Location

511.75.01012 Boehringer Ingelheim Investigational Site

Cincinnati, Ohio, United States

Location

511.75.01071 Boehringer Ingelheim Investigational Site

Cincinnati, Ohio, United States

Location

511.75.01038 Boehringer Ingelheim Investigational Site

Cleveland, Ohio, United States

Location

511.75.01048 Boehringer Ingelheim Investigational Site

Cleveland, Ohio, United States

Location

511.75.01061 Boehringer Ingelheim Investigational Site

Columbus, Ohio, United States

Location

511.75.01020 Boehringer Ingelheim Investigational Site

Tulsa, Oklahoma, United States

Location

511.75.01052 Boehringer Ingelheim Investigational Site

Eugene, Oregon, United States

Location

511.75.01059 Boehringer Ingelheim Investigational Site

Medfod, Oregon, United States

Location

511.75.01021 Boehringer Ingelheim Investigational Site

Portland, Oregon, United States

Location

511.75.01018 Boehringer Ingelheim Investigational Site

Jenkintown, Pennsylvania, United States

Location

511.75.01067 Boehringer Ingelheim Investigational Site

Columbia, South Carolina, United States

Location

511.75.01070 Boehringer Ingelheim Investigational Site

Greenville, South Carolina, United States

Location

511.75.01064 Boehringer Ingelheim Investigational Site

Knoxville, Tennessee, United States

Location

511.75.01049 Boehringer Ingelheim Investigational Site

Nashville, Tennessee, United States

Location

511.75.01013 Boehringer Ingelheim Investigational Site

Austin, Texas, United States

Location

511.75.01027 Boehringer Ingelheim Investigational Site

Dallas, Texas, United States

Location

511.75.01044 Boehringer Ingelheim Investigational Site

Fort Worth, Texas, United States

Location

511.75.01011 Boehringer Ingelheim Investigational Site

Houston, Texas, United States

Location

511.75.01055 Boehringer Ingelheim Investigational Site

San Antonio, Texas, United States

Location

511.75.01068 Boehringer Ingelheim Investigational Site

Waco, Texas, United States

Location

511.75.01007 Boehringer Ingelheim Investigational Site

Charlottesville, Virginia, United States

Location

511.75.01057 Boehringer Ingelheim Investigational Site

Norfolk, Virginia, United States

Location

511.75.01046 Boehringer Ingelheim Investigational Site

Richmond, Virginia, United States

Location

511.75.01019 Boehringer Ingelheim Investigational Site

Seattle, Washington, United States

Location

511.75.01036 Boehringer Ingelheim Investigational Site

Middleton, Wisconsin, United States

Location

511.75.02008 Boehringer Ingelheim Investigational Site

Coquitlam, British Columbia, Canada

Location

511.75.02002 Boehringer Ingelheim Investigational Site

North Vancouver, British Columbia, Canada

Location

511.75.02004 Boehringer Ingelheim Investigational Site

Woodstock, New Brunswick, Canada

Location

511.75.02005 Boehringer Ingelheim Investigational Site

Mount Pearl, Newfoundland and Labrador, Canada

Location

511.75.02010 Boehringer Ingelheim Investigational Site

Barrie, Ontario, Canada

Location

511.75.02011 Boehringer Ingelheim Investigational Site

London, Ontario, Canada

Location

511.75.02001 Boehringer Ingelheim Investigational Site

Ottawa, Ontario, Canada

Location

511.75.02007 Boehringer Ingelheim Investigational Site

Toronto, Ontario, Canada

Location

511.75.02012 Boehringer Ingelheim Investigational Site

Québec, Quebec, Canada

Location

511.75.02014 Boehringer Ingelheim Investigational Site

Québec, Quebec, Canada

Location

511.75.02009 Boehringer Ingelheim Investigational Site

Sherbrooke, Quebec, Canada

Location

511.75.02013 Boehringer Ingelheim Investigational Site

Trois-Rivières, Quebec, Canada

Location

511.75.02003 Boehringer Ingelheim Investigational Site

Saskatoon, Saskatchewan, Canada

Location

Related Publications (1)

• Thorp J, Simon J, Dattani D, Taylor L, Kimura T, Garcia M Jr, Lesko L, Pyke R; DAISY trial investigators. Treatment of hypoactive sexual desire disorder in premenopausal women: efficacy of flibanserin in the DAISY study. J Sex Med. 2012 Mar;9(3):793-804. doi: 10.1111/j.1743-6109.2011.02595.x. Epub 2012 Jan 12.

  PMID: 22239862 DERIVED

MeSH Terms

Conditions

Sexual Dysfunctions, Psychological

Interventions

flibanserin

Condition Hierarchy (Ancestors)

Mental Disorders

Results Point of Contact

• Title: Scientific Program Director
• Organization: Sprout Pharmaceuticals

clinicaltrials@sproutpharma.com

9198820850

Study Officials

• Boehringer Ingelheim

  Boehringer Ingelheim

  STUDY CHAIR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 3, 2006
• First Posted: August 4, 2006
• Study Start: July 1, 2006
• Primary Completion: March 1, 2008
• Study Completion: March 1, 2008
• Last Updated: June 27, 2016
• Results First Posted: June 27, 2016

Record last verified: 2016-06

Locations

US (64); CA (13)