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Completed

A Randomized, Double-blind, Placebo Controlled Study to Assess Efficacy, Safety and Tolerability of LCQ908 in Subjects With Familial Chylomicronemia Syndrome

NCT01514461

Conditions
Dyslipidemias, Familial Chylomicronemia Syndrome (FCS), Familial hyperchylomicronemia syndrome, +5 more
Locations
  • Novartis Investigative Site Seatlle, Washington, United States
  • Novartis Investigative Site Chicoutimi, Quebec, Canada
  • Novartis Investigative Site Ste-Foy, Quebec, Canada
  • Novartis Investigative Site Ouest-Montreal, Canada
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