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Dense Deposit Disease clinical trials

View clinical trials related to Dense Deposit Disease.

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NCT ID: NCT02302755 Withdrawn - Clinical trials for Dense Deposit Disease

TP10 Use in Patients With C3 Glomerulopathy (C3G)

Start date: November 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety of repeated TP10 dosing in pediatric and adult patients with C3G and to evaluate the activity of TP10 in pediatric and adult patients with C3G, as measured by the proportion of patients with normalization of serum C3, serum C3 breakdown products, or alternative pathway (AP) complement activity.

NCT ID: NCT01791686 Terminated - Clinical trials for Dense Deposit Disease

Clinical Trial of CDX-1135 in Pediatric and Adult Patients With Dense Deposit Disease

Start date: January 2013
Phase: Phase 1
Study type: Interventional

This study is evaluating the study drug (CDX-1135) in patients with dense deposit disease (DDD). The objective is to evaluate the safety and activity of repeated doses of CDX-1135 in pediatric and adult patients with DDD. After screening, eligible patients will be entered into the Induction Period. The Induction Period is up to 4 weeks. Following normalization of complement activity, patients will enter into the Maintenance Period.The total treatment duration is up to 26 weeks.

NCT ID: NCT01221181 Completed - Clinical trials for Dense Deposit Disease

Eculizumab Therapy for Dense Deposit Disease and C3 Nephropathy

Start date: July 2010
Phase: Phase 1
Study type: Interventional

This open label, non-blinded, proof of concept efficacy and safety study of eculizumab in patients with biopsy proven DDD or C3 nephropathy. The trial will consist of adult patients with these diseases who have > 1 gram of proteinuria or a decreased glomerular filtration rate (GFR), both predictors of a poor long-term outcome in many glomerular diseases. The patients will be treated with eculizumab for one year. The goals will be to determine whether treatment leads to an improvement in kidney function, defined by remissions of proteinuria and improvements in estimated GFR (measured by serum creatinine), and to improvement in histologic parameters, including percentage of non-affected glomeruli, interstitial fibrosis, intensity of C3 staining of immunofluorescence, and amount of electron dense deposits by electron microscopy.

NCT ID: NCT00583427 Withdrawn - Clinical trials for Dense Deposit Disease

Sulodexide Treatment in Patients With Dense Deposit Disease

Start date: December 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to see if a medicine called Sulodexide will help prevent or slow down the progression of Membranoproliferative Glomerulonephritis type II/Dense Deposit Disease. Sulodexide is not yet FDA approved and has not been studied in children. Study aim/hypotheses: to measure the efficacy of Sulodexide treatment in patients with the above disease/s.