Clinical Trials Directory

Trials / Completed

CompletedNCT00294671

The Effect of Diflunisal on Familial Amyloidosis

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
130 (actual)
Sponsor
Boston University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if diflunisal can prevent progressive lower leg nerve damage in patients with familial amyloidosis polyneuropathy. Funding Source - FDA Office of Orphan Products Development (OOPD); National Institute of Neurological Disorders and Stroke (NINDS)

Detailed description

Familial amyloidosis polyneuropathy (FAP) is a rare, lethal, autosomal dominant, neurodegenerative disease characterized by misfolding of variant transthyretin tetramer (TTR) - a transport protein produced by the liver. The disease causes TTR to become unstable, triggering amyloid fibrils to form and leading to peripheral and autonomic nerve dysfunction. Currently, the only treatment for FAP is a liver transplant, which is expensive and risk-filled. Medicines are needed to treat this disease. Previous in vitro (in a test tube) studies have shown that a common anti-inflammatory drug called diflunisal stabilizes TTR, preventing the formation of amyloid fibrils. The goal of this 2-year randomized, double-blind, placebo-controlled research study is to establish whether diflunisal can stop the nerve damage, or peripheral neuropathy, resulting from amyloid production in patients with FAP. Scientists already know that diflunisal prevents formation of amyloid in the test tube. This study will determine if the drug can block amyloid production in FAP patients. Participants will be randomly chosen to receive either diflunisal or an inactive (placebo) pill twice daily for 24 months. Participants will be carefully monitored through 7 follow-up visits, either at the study center or with individual primary care physicians. Participating in the study does not preclude patients from being listed for liver transplantation.

Conditions

Interventions

TypeNameDescription
DRUGdiflunisalgiven twice daily for 24 months
OTHERplaceboan inactive substance given twice daily for 24 months

Timeline

Start date
2006-02-01
Primary completion
2012-12-01
Completion
2012-12-01
First posted
2006-02-22
Last updated
2017-03-17
Results posted
2017-03-17

Locations

8 sites across 5 countries: United States, Italy, Japan, Sweden, United Kingdom

Source: ClinicalTrials.gov record NCT00294671. Inclusion in this directory is not an endorsement.