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Clinical Trial Summary

Chronic liver diseases are often characterized by portal hypertension, a major complication involving haemodynamic changes due to increased intrahepatic vascular resistance. It has become well established that nitric oxide (NO) plays a crucial role in the haemodynamic abnormalities that develop in chronic portal hypertension.

NCX-1000 is a NO-releasing derivative of ursodeoxycholic acid that would compensate for the defective liver NO production in cirrhosis.

This study intends to demonstrate the desired therapeutic activity (reduction in portal pressure) in a small number of target patients, to assess the safety and tolerability after repeated oral administrations of NCX-1000, and to get preliminary pharmacokinetic data in this population.


Clinical Trial Description

Brief summary is complete. Study is closed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00414869
Study type Interventional
Source Forest Laboratories
Contact
Status Terminated
Phase Phase 2
Start date November 2005
Completion date February 2007

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