Status:
COMPLETED
Study to Investigate the Efficacy and Safety of Vardenafil Flexible Dose Versus Placebo in Males With Erectile Dysfunction
Lead Sponsor:
Bayer
Collaborating Sponsors:
GlaxoSmithKline
Conditions:
Erectile Dysfunction
Eligibility:
MALE
18+ years
Phase:
PHASE3
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.
Eligibility Criteria
Inclusion
- 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
- 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%.
- D) Other
Key Trial Info
Start Date :
October 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2004
Estimated Enrollment :
229 Patients enrolled
Trial Details
Trial ID
NCT00657033
Start Date
October 1 2003
End Date
August 1 2004
Last Update
October 14 2013
Active Locations (26)
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1
Phoenix, Arizona, United States, 85023
2
Beverly Hills, California, United States, 90212
3
Irvine, California, United States, 92618-3603
4
Newport Beach, California, United States, 92660