Mönchengladbach, North Rhine-Westphalia, 41061, Germany
NCT Number: NCT01110590
Multiple Dose Escalation Study (14 Days) to Investigate Safety, Tolerability, PK and PD of Vardenafil and BAY60-4552
Safety, tolerability, pharmacokinetics and pharmacodynamics will be investigated in this multiple dose escalation study. In three treatments groups different dosages of BAY 60-4552 and vardenafil will be given with patients with erectile dysfunction.
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Notify MeKey information
Conditions
Age range
18 year–70 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 1
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- The informed consent must be signed before any study specific tests or procedures are done
- Male patients with a history of erectile dysfunction (ED) for at least 6 months, defined as "the inability to achieve and maintain an erection of the penis sufficient to complete satisfactory sexual intercourse" by the NIH consensus report 1993. The diagnosis of 'Erectile dysfunction' has to be confirmed by a physician
- Age: 18 to 70 years (inclusive) at the first screening examination
- Ethnicity: White
- Body mass index (BMI): equal to or above 18 and below 32 kg / m²
- Confirmation of the patient's health insurance coverage prior to the first screening examination / visit
- Ability to understand and follow study-related instructions
Exclusion criteria
- Incompletely cured pre-existing diseases for which it can be assumed that the absorption, distribution, metabolism, elimination and effects of the study drugs will not be normal
- Known hypersensitivity to the study drugs (active substances or excipients of the preparations)
- Known severe allergies, non-allergic drug reactions, or multiple drug allergies
- Any underlying cardiovascular condition, including unstable angina pectoris that would preclude sexual activity according to the NIH consensus report 1993
- History of myocardial infarction, stroke or life-threatening arrhythmia within 6 months prior to screening
- Bleeding disorder
- History of prostatectomy because of prostate cancer, including nerve-sparing techniques. Clarification: Any surgical procedures for the treatment of Benign Prostate Hypertrophy (BPH) are permitted, with the exception of cryosurgery, cryotherapy or cryoablation
- Hereditary degenerative retinal disorders such as retinitis pigmentosa
- History of loss of vision because of NAION (Bayer Study 12912), temporary or permanent loss of vision, including unilateral loss of vision
- History of uni- or bilateral hearing loss
Treatment and study plan
BAY60-4552 + Vardenafil
DrugTotal dose given over 14 days: 5.25 mg BAY60-4552 + 140 mg Vardenafil
Placebo
DrugPlacebo
Primary outcomes
-
Adverse Event reporting
Time frame: up to 6 weeks
Secondary outcomes
-
Plasma concentration of study drugs; Pharmacokinetic parameters: AUC, Cmax, AUC/D, Cmax;norm, Cmax/D, t1/2, tmax
Time frame: Day 0, 6, 13
-
Plasma concentration of cyclic guanosine monophosphate (cGMP)
Time frame: Day 0, 6, 13
Sponsors and collaborators
Lead sponsor
Bayer
Industry
Registry information
Official study title
Randomized, Double-blind, Placebo-controlled, Group-comparison, Dose-escalation Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Co-administration of Different Doses of Vardenafil (2 Dose Strengths) and BAY60-4552 (4 Dose Strengths) Given Once-daily (od) Over 14 Days in Patients With Erectile Dysfunction (ED).
Important dates
- Study start
- 2010
- Primary completion
- 2010
- Study completion
- 2010
- First posted
- Apr 26, 2010
- Registry last updated
- Feb 22, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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