Clinical Proof-of-concept Study for the Combination BAY60-4552 / Vardenafil for the Treatment of Erectile Dysfunction Not Sufficiently Responsive to Standard Therapy With PDE5 Inhibitors

This is an interventional treatment trial for Erectile Dysfunction focused on measuring Combination Drug Therapy, Phosphodiesterase inhibitors Read More

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