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NCT07727538Possibly a fitRecruiting

Olezarsen for familial chylomicronemia syndrome in children and teens

Familial Chylomicronemia Syndrome

Part of Genetic & congenital, Hormones & metabolism clinical trials.

This study tests a new medicine called olezarsen to lower very high triglycerides (fats) in the blood of children and teenagers with familial chylomicronemia syndrome (FCS), a rare genetic condition. The goal is to reduce the risk of pancreatitis and other complications.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
12 people
Ages
2 years to 17 years
Study type
Interventional

Who can take part

  • The child must be between 2 and 17 years old (with parent or guardian consent).
  • A confirmed genetic diagnosis of familial chylomicronemia syndrome (FCS) is required.
  • Fasting triglyceride levels must be at least 880 mg/dL (about 10 mmol/L) at screening.
  • The child must be willing to fast for at least 10 hours before certain blood tests.
  • No recent pancreatitis, major surgery, or use of other investigational drugs within the specified timeframes.

View the official record on ClinicalTrials.gov

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