A Study of Olezarsen for Familial Chylomicronemia Syndrome (FCS) in Children
This study is testing a drug called olezarsen for children aged 2 to 17 years old who have Familial Chylomicronemia Syndrome (FCS). FCS is a rare genetic condition that causes very high levels of fats (triglycerides) in the blood. Olezarsen is given as a shot under the skin. The main goal is to see how much olezarsen can lower fasting triglycerides after 6 months. The study is currently enrolling about 12 participants. To join, a parent or guardian must give permission, and the child must also agree if they are old enough to understand. You must also be able to follow all study procedures.
- Study design
- This is a Phase 3, multi-center, open-label study, meaning both you and the study team will know you are receiving olezarsen. It plans to enroll about 12 participants.
- What's involved
- The study involves a 1-month screening period, a 1-year treatment period, an optional 1-year extension, and a 3-month follow-up period.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 3 months after their treatment period ends.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study of Olezarsen for the Treatment of Familial Chylomicronemia Syndrome (FCS) in Pediatric Participants
At a glance
Conditions
Where it's being run
3 sites across 2 statesWho to contact
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What this trial measures
- Percent Change from Baseline in Fasting Triglycerides (TG)At 6 Months