check_circleStudy Completed

Erectile Dysfunction

BAY38-7268, 20 mg Pharmburst FDT vs 20 mg Levitra

Trial purpose

Please see attached Study Results Summary below

Key Participants Requirements

Sex

N/A

Age

22 - 47 Years
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Trial summary

Enrollment Goal
12
Trial Dates
September 2004 - October 2004
Phase
Phase 1
Could I Receive a placebo
N/A
Products
Levitra (Vardenafil, BAY38-9456)
Accepts Healthy Volunteer
N/A

Where to participate

StatusInstitutionLocation
Completed
MEDA Manufacturing GmbH, ClinPharmCologneKöln, 51063, Germany

Trial design

Randomized, two-fold crossover study to investigate the relative bioavailability of 20 mg vardenafil oral disintegrating tablet in comparison to a 20 mg vardenafil standard tablet after single oral dosing in healthy male subjects
Trial Type
Interventional
Intervention Type
N/A
Trial Purpose
N/A
Allocation
N/A
Blinding
N/A
Assignment
N/A
Trial Arms
N/A