Study of Efficacy of a Vasopressin 2 Receptor Antagonist M0002 for Treatment of Ascites in Cirrhotic Subjects With Hypo- or Normonatraemia
This study has been completed.
Sponsor:
Movetis
Information provided by:
Movetis
ClinicalTrials.gov Identifier:
NCT01179607
First received: August 10, 2010
Last updated: NA
Last verified: July 2010
History: No changes posted
| Tracking Information | |
|---|---|
| First Received Date ICMJE | August 10, 2010 |
| Last Updated Date | August 10, 2010 |
| Start Date ICMJE | June 2007 |
| Primary Completion Date | December 2007 (final data collection date for primary outcome measure) |
| Current Primary Outcome Measures ICMJE |
Plasma sodium levels, weight, number of paracentesis [ Time Frame: 15 days ] [ Designated as safety issue: No ] |
| Original Primary Outcome Measures ICMJE | Same as current |
| Change History | No Changes Posted |
| Current Secondary Outcome Measures ICMJE | Not Provided |
| Original Secondary Outcome Measures ICMJE | Not Provided |
| Current Other Outcome Measures ICMJE | Not Provided |
| Original Other Outcome Measures ICMJE | Not Provided |
| Descriptive Information | |
| Brief Title ICMJE | Study of Efficacy of a Vasopressin 2 Receptor Antagonist M0002 for Treatment of Ascites in Cirrhotic Subjects With Hypo- or Normonatraemia |
| Official Title ICMJE | 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. |
| Brief 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. |
| Detailed Description | Not Provided |
| Study Type ICMJE | Interventional |
| Study Phase | Phase 2 |
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Condition ICMJE | Cirrhotic Ascites |
| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided |
|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
|
| Recruitment Information | |
| Recruitment Status ICMJE | Completed |
| Enrollment ICMJE | 15 |
| Completion Date | December 2007 |
| Primary Completion Date | December 2007 (final data collection date for primary outcome measure) |
| Eligibility Criteria ICMJE | Main Inclusion Criteria:
Main Exclusion Criteria:
|
| Gender | Both |
| Ages | 18 Years to 75 Years |
| Accepts Healthy Volunteers | No |
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects |
| Location Countries ICMJE | Not Provided |
| Administrative Information | |
| NCT Number ICMJE | NCT01179607 |
| Other Study ID Numbers ICMJE | M0002-BEL-C201 |
| Has Data Monitoring Committee | No |
| Responsible Party | Movetis |
| Study Sponsor ICMJE | Movetis |
| Collaborators ICMJE | Not Provided |
| Investigators ICMJE | Not Provided |
| Information Provided By | Movetis |
| Verification Date | July 2010 |
|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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