Research

Carbamazepine for Liver Disease due to Antitrypsin Deficiency – Pilot Trial

A Preliminary Study of the Efficacy and Safety of Carbamazepine in Severe Liver Disease Due to Alpha-1-Antitrypsin Deficiency

Protocol Description

This research study, being carried out at Children’s Hospital of Pittsburgh of UPMC and Presbyterian Hospital of UPMC, is designed to determine whether carbamazepine (CBZ), a drug which has been used safely for many years for seizures and depression, can reduce the severity of liver disease that occurs in some people with the genetic disorder known as Alpha-1 Antitrypsin deficiency (ATD). In this disorder a genetic mutation results in the formation of an abnormal protein that accumulates in liver cells. This accumulation is toxic to the liver cells and therefore leads to gradual scarring and ultimately failure of the liver to function properly. Researchers from CHP have shown that CBZ stimulates a process that removes abnormal proteins from cells in animal models of ATD. CBZ, also known by the trade name Tegretol XR, is currently FDA approved for use by children in the treatment of seizures, depression and facial pain due to nerve inflammation.

Study Level: Pilot

Eligibility Criteria

Subject to certain exclusion criteria, this study is accepting patients of both genders, ages 14 and up, with liver disease due to ATD.
Males: 14 years and older
Females: 14 years and older

Requirements
Participants will be randomly assigned to groups that will either take CBZ or a placebo, prepared in identical appearing capsules. Two thirds of the subjects will take CBZ and one-third will take placebo. Dosages will be increased weekly for the first five weeks, and monitoring of the drug level in the blood will be done throughout the study to reduce side effects. Liver biopsies and measurement of liver pressure will be done at the beginning of the study and at week 52, after which the study medication will be stopped. However monitoring, including blood tests, will continue at intervals through the second year.
Visits: At least 13
Duration: Approximately 2 years

Status: Open for Enrollment

Source(s) of Support
National Institutes of Health
Novartis

Additional Resources
Study Description at National Institutes of Health
Spotlight Feature and Video
News Release about this Study

Primary Investigator(s)

David H. Perlmutter, MD

Contact Information

For information or to enroll, please contact:
Erin Sandene, RN, BSN, CCRC
412 692-6558
erin.sandene@chp.edu

Last Update
March 13, 2014
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Last Update
March 13, 2014
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