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

Bayer

Status and phase: Completed; Phase 2

Conditions: Erectile Dysfunction

Treatments: Drug: Vardenafil; Drug: BAY60-4552 plus Vardenafil; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT01168817

2010-020122-18 (EudraCT Number)

14694

Details and patient eligibility

About

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.

Enrollment: 140 patients

Sex: Male

Ages: 18 to 64 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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140 participants in 3 patient groups, including a placebo group

Arm 1

Experimental group

Treatment:

Drug: BAY60-4552 plus Vardenafil

Arm 2

Active Comparator group

Treatment:

Drug: Vardenafil

Arm 3

Placebo Comparator group

Treatment:

Drug: Placebo