drugset / Trial / NCT01843790

A Phase 2a Study of Weekly Doses of GCS-100 in Patients With Chronic Kidney Disease

NCT01843790 ↗

Phase 2 Completed 120 enrolled La Jolla Pharmaceutical Company
RandomizedParallel-groupSingle-blindTreatment

Summary

The primary objective of this study is to compare the change in estimated glomerular filtration rate (eGFR) from baseline to Week 8 between placebo and GCS-100 treatment. The secondary objective is to determine the safety and tolerability of GCS-100 administered for 8 weeks relative to placebo. In addition, the study will measure the effect of GCS-100 on circulating galectin-3 and other markers of disease activity.

Timeline

Start
2013-06
Primary completion
2014-02
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Subject GCS-100 Unknown — Intravenous