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Clinical Trial Summary

Patients with familial dysbetalipoproteinemia (FD) have increased triglycerides, non-high-density lipoprotein cholesterol (non-HDL-C), beta VLDL, premature atherosclerosis and cardiovascular disease. They also have a delayed postprandial triglyceride and chylomicron (CM) remnant clearance. Postprandial hypertriglyceridemia is associated with increased vascular risk. Although combination therapy with statin and fibrate is recommended in the treatment of patients with FD, there is still a substantial amount of patient who do not reach their treatment target with this medication. Furthermore no information is available about the postprandial effects of adding evocolumab to standard lipid lowering therapy in FD patients.


Clinical Trial Description

See brief summary ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03811223
Study type Interventional
Source UMC Utrecht
Contact Frank LJ Visseren, prof
Phone +31 88 7557324
Email f.l.j.visseren@umcutrecht.nl
Status Not yet recruiting
Phase Phase 4
Start date August 2019
Completion date March 2021

See also
  Status Clinical Trial Phase
Terminated NCT00145431 - Study To Evaluate The Effect Of Torcetrapib/Atorvastatin In Subjects With A Genetic Cholesterol Disorder. Phase 3
Completed NCT00214604 - Type III Dysbetalipoproteinemia Phase 3