Clinical Trials Directory

Trials / Completed

CompletedNCT01409148

Radioimmunoimaging of AL Amyloidosis

Radioimmunoimaging (PET/CT) of Patients With AL Amyloidosis Using the 124I-Labeled Amyloid-Reactive Monoclonal Antibody Mu 11-1F4

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
38 (actual)
Sponsor
University of Tennessee · Academic / Other
Sex
All
Age
21 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to determine the capability of a radiolabeled amyloid-reactive monoclonal antibody to document the presence and distribution of amyloid deposits by PET/CT imaging in patients with AL amyloidosis.

Detailed description

To be eligible for this study, patients must have a confirmed diagnosis of AL amyloidosis without significant cardiac (New York Heart Association class IV) disease and not be on kidney dialysis. Additionally, after testing, their blood must not contain antibodies to mouse proteins. The study requires an intravenous infusion, over 10 minutes, of the radiolabeled antibody, followed 48 hours later by a PET/CT scan. A repeat scan is done 5 or 7 days after infusion of the antibody. A 5 ml blood specimen needs to be furnished 4 and 8 weeks after the antibody infusion.

Conditions

Interventions

TypeNameDescription
BIOLOGICAL124I-labeled monoclonal antibody Mu 11-1F4Single infusion of radiolabeled antibody: 2mCi (1 mg)

Timeline

Start date
2008-11-01
Primary completion
2012-03-01
Completion
2012-03-01
First posted
2011-08-04
Last updated
2012-10-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01409148. Inclusion in this directory is not an endorsement.