drugset / Trial / NCT01146522

Safety, Tolerability,Pharmacokinetics(PK)and Pharmacodynamics(PD)Assessment of LCQ908 in Patients With Severe Hypertriglyceridemia

NCT01146522

Phase 1/2 Completed 8 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will assess safety, tolerability, and effect of LCQ908 on blood lipids in patients with severe hypertriglyceridemia.

Timeline

Start
2010-05
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Pradigastat Small molecule 10 mg Oral
Subject Pradigastat Small molecule 20 mg Oral
Subject Pradigastat Small molecule 40 mg Oral

Indications