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Trials / Completed

CompletedNCT01179607

Study of Efficacy of a Vasopressin 2 Receptor Antagonist M0002 for Treatment of Ascites in Cirrhotic Subjects With Hypo- or Normonatraemia

A Randomized, Double Blind, Placebo Controlled, Phase II, Dose-titration Trial to Explore the Safety, Tolerability, Pharmacokinetic Profile and Efficacy of M0002 in Cirrhotic Subjects With Ascites and Hypo- or Normonatraemia.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Movetis · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

M0002, an orally active, selective non-peptidergic antagonist of the vasopressin V2 receptor inhibits vasopressin-induced water reabsorption from the kidney. Therefore the aquaretic effect of M0002 has a potential clinical benefit in the treatment of ascites and hyponatreamia in cirrhotic patients.

Conditions

Interventions

TypeNameDescription
DRUGM0002
DRUGPlacebo

Timeline

Start date
2007-06-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2010-08-11
Last updated
2010-08-11

Source: ClinicalTrials.gov record NCT01179607. Inclusion in this directory is not an endorsement.

Study of Efficacy of a Vasopressin 2 Receptor Antagonist M0002 for Treatment of Ascites in Cirrhotic Subjects With Hypo- (NCT01179607) · Clinical Trials Directory