A double-blind, placebo-controlled dose response study to investigate pharmacodynamics and pharmacokinetics of single and repeated oral doses of VA106483 in elderly male subjects

Registry ID

EUCTR2008-003774-17

Source registry

EUCTR

Status

Completed

Phase

PHASE2

Sponsor

Vantia Ltd

Start date

2008-07-03

Completion date

2009-02-02

Last update

2026-08-16

Conditions

• Nocturia.

Summary

To determine the pharmacodynamic profile of VA106483 including urinary volume, urinary osmolality, blood pressure, pulse rate, serum electrolytes and blood coagulation factors in elderly male subjects. To determine the pharmacokinetic profile of VA106483 in elderly male subjects.

Locations

• , , UK

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