The purpose of this study is to establish the dose response relationship of VA106483 and
nocturnal urine volumes in a population of elderly male subjects with Benign Prostatic
Hypertrophy (BPH) who are likely to present with nocturia.
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Full eligibility criteria for NCT01330927
Ages eligible for Study
65 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Males aged 65 years old and above with history of nocturia and benign prostatic hypertrophy (BPH)
Administration of any Investigational Medicinal Product (IMP) within 10 weeks before entry to the study
Any clinically significant concomitant medical disease, condition or abnormal laboratory test result
Other protocol defined eligibility criteria may apply
All locations for NCT01330927
Early Phase Clinical Unit, PAREXEL International GmbH
Berlin, Germany, 14050
View full eligibility
Tris trial is registered with FDA with number: NCT01330927. The sponsor of the trial is Vantia Ltd and it is looking for 30 volunteers for the current phase.
Official trial title: A Randomised, Double-blind, Placebo-controlled, Five-way Cross-over Dose Response Study to Determine the Effect of VA106483 on Nocturnal Urine Volume in Elderly Male Subjects With Nocturia and Benign Prostatic Hypertrophy (BPH)
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