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NCT01280188

Peroral Administration of Different Doses of Desmopressin Administered as a New Orally-Disintegrating Tablet and Desmopressin for Nasal Administration in the Treatment of CDI in Japanese Patients

Completed Phase 3 Last updated 10 August 2012
What this trial tests

Phase 3 trial testing Desmopressin Oral Melt in Central Diabetes Insipidus in 20 participants. Completed in 1 August 2012.

Timeline
1 January 2011
Primary endpoint
1 August 2011
1 August 2012

Quick facts

Lead sponsorFerring Pharmaceuticals
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment20
Start date1 January 2011
Primary completion1 August 2011
Estimated completion1 August 2012
Sites5 locations across Japan

Drugs / interventions tested

Conditions studied

Sponsor

Ferring Pharmaceuticals — full company profile →

Who can join

Adults 6 to 75, any sex, with Central Diabetes Insipidus. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This is an open-label dose-titration study in Japanese Central Diabetes Insipidus (CDI) patients designed to demonstrate the efficacy and safety of orally-disintegrating tablet of desmopressin.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Ferring Pharmaceuticals trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01280188.

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