Study to Investigate the Efficacy and Safety of Vardenafil Flexible Dose Versus Placebo in Males With Erectile Dysfunction

NCT ID: NCT00657033

Last Updated: 2013-10-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 229 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-10-31
• Study Completion Date: 2004-08-31

Brief Summary

Study to investigate the efficacy and safety of vardenafil flexible dose versus placebo in males with erectile dysfunction, and their female partners' sexual quality of life.

Conditions

Erectile Dysfunction

Keywords

Erectile Dysfunction

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Arm 1

Group Type: EXPERIMENTAL

Levitra (Vardenafil, BAY38-9456)

Intervention Type: DRUG

BAY 38-9456 (Vardenafil) will be supplied as 5 mg tablets, 10 mg tablets, and 20 mg tablets.

Arm 2

Group Type: EXPERIMENTAL

Placebo

Intervention Type: DRUG

Identical placebo tablets will be matched for each vardenafil dosage and will be indistinguishable from active treatment

Interventions

Levitra (Vardenafil, BAY38-9456)

BAY 38-9456 (Vardenafil) will be supplied as 5 mg tablets, 10 mg tablets, and 20 mg tablets.

Intervention Type: DRUG

Placebo

Identical placebo tablets will be matched for each vardenafil dosage and will be indistinguishable from active treatment

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Males who have had ED for at least six months according to the National Institutes of Health (NIH) Consensus Conference December 7-9, 1992 (inability to attain and/or maintain penile erection sufficient for satisfactory sexual performance).
• Stable, heterosexual relationship for more than 6 months.
• Males 18 years, and older.
• Written informed consent obtained.
• The subject and his female partner must make at least four attempts at sexual intercourse on four separate days during the untreated baseline period (according to the answer to the following question in the Patient Diary: "Was sexual activity initiated with the intention of intercourse?").
• At least 50% of attempts at sexual intercourse during the untreated baseline period must be unsuccessful, according to the following questions from the subject diary (at least one question should be answered "No"): "Were you able to achieve at least some erection (some enlargement of the penis)?"; "Were you able to insert your penis in your partner's vagina?"; "Did your erection last long enough for you to have successful intercourse?".

Exclusion Criteria

A) Previous or current medical conditions:

• Any unstable medical, psychiatric, or substance abuse disorder that in the opinion of the Investigator is likely to affect the subject's ability to complete the study or precludes the subject's participation in the study.
• Presence of penile anatomical abnormalities (e.g. penile fibrosis or Peyronie's disease) which, in the Investigator's opinion, would significantly impair erectile function.
• Primary hypoactive sexual desire.
• Spinal cord injury.
• History of surgical prostatectomy (excluding TURP).
• Retinitis pigmentosa.
• Unstable angina pectoris.
• History of myocardial infarction, stroke or life-threatening arrhythmia within the prior 6 months.
• Uncontrolled atrial fibrillation/flutter at screening (ventricular response rate ≥ 100 bpm).
• Severe chronic or acute liver disease, history of moderate or severe hepatic impairment.
• Clinically significant chronic haematological disease which may lead to priapism such as sickle cell anemia and leukemia.
• Bleeding disorder.
• Significant active peptic ulcer disease.
• Resting hypotension (a resting systolic blood pressure of < 90 mm Hg) or hypertension (a resting systolic blood pressure > 170 mm Hg or a resting diastolic blood pressure > 110 mm Hg).
• History of malignancy within the past 5 years (other than squamous or basal cell skin cancer).
• NYHA Class III and IV heart failure.
• History of positive test for Hepatitis B surface antigen (HBsAg) or Hepatitis C.
• Symptomatic postural hypotension within 6 months of visit 1.

B) Concomitant medication:

• Subjects who are taking nitrates or nitric oxide donors.
• Subjects who take anticoagulants, except for antiplatelet agents.
• Subjects who are taking androgens.
• Subjects who are taking anti-androgens.
• Subjects who are taking the following inhibitors of cytochrome P450 3A4: very potent HIV protease inhibitors (ritonavir, indinavir), the anti-mycotic agents itraconazole and ketoconazole (topical forms are allowed) or erythromycin.
• Subjects who have received any investigational drug (including placebo) within 30 days of Visit 1.
• Use of any treatment for ED within 7 days of visit 1 or during the study, including oral medications, vacuum devices, constrictive devices, injections or urethral suppositories.
• Subjects who are taking alpha blockers

C) Abnormal laboratory values:

• Subjects who have a serum total testosterone level more than 25% below the age-adjusted lower limit of normal according to the range of the testing laboratory.
• Subjects with a serum creatinine > 3.0 mg/dl.
• Elevation of AST and/or ALT > 3 times the upper limit of normal.
• Diabetic subjects with an HbA1c>12%.

• Subjects age 65 or older who in the judgment of the investigator can not be started on a 10 mg dose
• Subjects with a history of unresponsiveness to any PDE 5 Inhibitor treatment due to lack of efficacy or significant side effects leading to discontinuation of the PDE 5 Inhibitor treatment.
• Subjects unwilling to cease use of vacuum devices, intracavernosal injections, Viagra® or other therapy for ED during the study.
• Unwillingness of the subject or his partner to make 4 attempts at sexual intercourse on four separate days during the untreated baseline period.
• Subjects with known hypersensitivity to Vardenafil, Bay 38-9456 (also known as SB-782528) or any component of the investigational medication.
• Subjects who are illiterate or unable to understand the questionnaires or the Patient Diary.
• Partners who are illiterate or unable to understand the questionnaires.
• Subjects who are unwilling or unable to complete the Patient Diary.
• Subjects or partners who, in the opinion of the investigator, would be non-compliant with the visit schedule of study procedures.
• Subjects unwilling to refrain from consuming grapefruit juice or products containing grapefruit juice with study medication (Canada only).

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

GlaxoSmithKline

INDUSTRY

Sponsor Role: collaborator

Bayer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bayer Study Director

Role: STUDY_DIRECTOR

Bayer

Locations

Phoenix, Arizona, United States

Beverly Hills, California, United States

Irvine, California, United States

Newport Beach, California, United States

San Bernardino, California, United States

San Diego, California, United States

San Diego, California, United States

Trumbull, Connecticut, United States

Jacksonville, Florida, United States

Riverdale, Georgia, United States

Greenbelt, Maryland, United States

Lutherville, Maryland, United States

Lawrenceville, New Jersey, United States

New Brunswick, New Jersey, United States

New York, New York, United States

Charlotte, North Carolina, United States

Statesville, North Carolina, United States

Wilmington, North Carolina, United States

Calgary, Alberta, Canada

Barrie, Ontario, Canada

Burlington, Ontario, Canada

Kitchener, Ontario, Canada

London, Ontario, Canada

Oakville, Ontario, Canada

Saskatoon, Saskatchewan, Canada

Victoria, , Canada

Countries

United States; Canada

Other Identifiers

100519

Identifier Type: -

Identifier Source: org_study_id