Clin2
NCT05682378Possibly a fitRecruiting

Long-term follow-up for inclisiran in young people with inherited high cholesterol

Heterozygous or Homozygous Familial Hypercholesterolemia

Treatments studied

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

This study follows people with HeFH or HoFH (inherited high cholesterol) who previously took inclisiran in specific pediatric ORION studies. It mainly checks long-term safety and how well the treatment continues to be tolerated over time.

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

Phase
Phase 3
Enrollment
195 people
Ages
12 years to 100 years
Study type
Interventional

Who can take part

  • You have been diagnosed with HeFH or HoFH (inherited high cholesterol)
  • You already finished one of the pediatric ORION studies: ORION-16, ORION-13, ORION-20, or ORION-19
  • Your study doctor feels you benefited from inclisiran during the earlier ORION study
  • You did not “screen fail” and did not permanently stop the earlier study
  • You did not have serious safety or tolerability problems linked to inclisiran in the earlier study
  • You do not have any serious or uncontrolled medical issue that would interfere with the study or increase risk

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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