drugset / Trial / NCT01589237

Extension to a Randomized, Double-blind, Placebo Controlled Study of LCQ908 in Subjects With Familial Chylomicronemia Syndrome.

NCT01589237

Phase 3 Terminated 38 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study was to determine long-term safety and tolerability, and continued efficacy in lowering triglycerides of LCQ908 in subjects with Familial Chylomicronemia Syndrome (FCS) (HLP type I).

Timeline

Start
2013-02
Primary completion
2015-07
Completion
2015-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Pradigastat Small molecule 10 mg