Erectile Dysfunction
Conditions
Keywords
Combination Drug Therapy, Phosphodiesterase inhibitors
Brief summary
This study examines the efficacy and safety of the combination treatment BAY60-4552 plus vardenafil in patients with erectile dysfunction, who do not sufficiently respond to therapy with PDE5 (Phosphodiesterase 5) inhibitors. Patients meeting the entry criteria, will receive vardenafil alone in the first four weeks of the study to assess the effect of PDE5 inhibitor therapy given alone. Patients with an insufficient therapeutic response to vardenafil alone will enter the next part of the study, and will be randomly assigned to one of 3 treatments. There is a 1 in 3 chance of receiving either the combination BAY60-4552 plus vardenafil, or vardenafil alone, or placebo. Neither patient nor the treating physician will know which treatment is given (double-blinded design).This part of the study will last four weeks Patients will have to go to the clinic/hospital for 7 visits during the 8 weeks.
Interventions
DRUGBAY60-4552 plus Vardenafil
Treatment with 3 tablets once daily for 4 weeks (Vardenafil 10 mg plus BAY60-4552 1.0 mg)
DRUGVardenafil
Treatment with 3 tablets once daily for 4 weeks (Vardenafil 20 mg)
DRUGPlacebo
Treatment with 3 tablets once daily for 4 weeks (Placebo)
Sponsors
Bayer
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
MALE
Age
18 Years to 64 Years
Healthy volunteers
No
Inclusion criteria
* Open-label run-in phase (first four weeks): * Written informed consent signed before any study-specific procedure * History of ED (Erectile Dysfunction) for at least 6 months prior to screening, defined as the inability to achieve and maintain an erection of the penis sufficient to complete satisfactory sexual intercourse; the diagnosis of ED has to be confirmed by a physician * Stable, heterosexual relationship for at least 6 months prior to screening * Aged 18 to 64 years (inclusive) at the first screening examination * History of previous use of at least 1 marketed PDE5 (Phosphodiesterase 5) inhibitor and insufficient therapeutic efficacy despite use of the highest approved dose * Double-blind treatment phase (last four weeks): * At least 4 attempts at sexual intercourse on 4 separate days during the open-label run-in phase with use of 20 mg vardenafil approximately 1 hour before attempting intercourse * IIEF EF (International Index of Erectile Function - Erectile Function subscale) score \<17 * At least 50% of attempts at sexual intercourse during the open-label run-in phase were unsuccessful
Exclusion criteria
* Contraindication to use of vardenafil * History of prostatectomy due to prostate cancer, including nerve-sparing techniques. * Concomitant use of adrenergic blockers * History of spinal cord injury * Resting hypotension, i.e. SBP (Systolic Blood Pressure) \<100 mmHg at rest * Moderate / severe hypertension, i.e. SBP \>170 mmHg or DBP \>110 mmHg at rest * Symptomatic orthostatic hypotension with a decrease in SBP \>20 mmHg or in DBP (Diastolic Blood Pressure) \>10 mmHg subsequent to change from the supine to standing position
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of erectile dysfunction assessed by the IIEF-EF (International Index of Erectile Function - Erectile Function subscale) | Week 4 |
Secondary
| Measure | Time frame |
|---|---|
| Success rate assessed by subject diary question: 'Maintenance' (Did your erection last long enough to have sexual intercourse?) | Week 4 |
| Success rate assessed by subject diary question: Penetration' (Were you able to insert your penis into your partner's vagina?) | Week 4 |
Countries
Finland, France, Germany, Italy, Netherlands, Spain, Sweden
Outcome results
None listed