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An Extension Study Investigating the Efficacy and Safety of a Fast-Dissolving ("Melt") Formulation of Desmopressin for the Treatment of Nocturia in Adults

2014-08-27 03:32:57 | BioPortfolio

Summary

The purpose of this study is to investigate the efficacy and safety of several doses of the melt formulation of desmopressin in a broad population of adult patients with nocturia.

Description

The objective of the present study is to investigate the long-term efficacy and safety of the melt formulation of desmopressin.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Conditions

Nocturia

Intervention

lyophilisate oral of desmopressin, lyophilisate oral of desmopressin, lyophilisate oral of desmopressin, lyophilisate oral of desmopressin

Location

Radiant Research
Scottsdale
Arizona
United States
85251

Status

Completed

Source

Ferring Pharmaceuticals

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:32:57-0400

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