Study of the Safety and Efficacy of NC-503 in Secondary (AA) Amyloidosis

Completed · Phase 2/Phase 3

Conditions studied: Secondary (AA) Amyloidosis, Rheumatoid Arthritis, Nephrotic Syndrome, Familial Mediterranean Syndrome, Kidney Diseases, Gastrointestinal Diseases

In brief

The main objective of this study is to evaluate the safety and efficacy of NC-503 compared to placebo in patients with secondary (AA) amyloidosis using a composite assessment of clinical improvement/worsening of both renal and gastrointestinal functions.

Key facts

Study ID
NCT00035334
Run by
Bellus Health Inc. - a GSK company
People needed
150
Starts
2001-10-01
Expected to finish
2004-12-01
Last updated by the study team
2006-02-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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