The purpose of this study is to assess safety and efficacy of CAT-2003 in patients with chylomicronemia. The study will evaluate the effects of CAT-2003 on fasting total and chylomicron triglyceride levels, as well as postprandial total and chylomicron triglyceride clearance. This is a single-blind study. All patients will receive placebo for 1 week, and CAT-2003 for 12 weeks during the 13 week treatment period.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
13
Unnamed facility
Chicoutimi, Quebec, Canada
Unnamed facility
Québec, Quebec, Canada
Percent change from baseline in fasting triglycerides in patients with chylomicronemia
Time frame: 12 Weeks
Absolute and percent change from baseline on postprandial total and chylomicron triglyceride levels
Time frame: 12 Weeks
Absolute and percent change from baseline on chylomicron triglyceride clearance
Time frame: 12 Weeks
Absolute and percent change from baseline in plasma non-HDL-C
Time frame: 12 Weeks
Frequency of adverse events
Time frame: 13 weeks
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