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NCT07450378Possibly a fitNot yet recruiting

Study of an investigational medicine for inherited high cholesterol

Heterozygous Familial Hypercholesterolemia (HeFH)

Treatments studied

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

This study tests an investigational medicine called QLC7401 for people with a genetic condition called heterozygous familial hypercholesterolemia, which causes very high cholesterol. It aims to see if the new medicine can further lower bad cholesterol when added to your usual cholesterol treatments.

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

Phase
Phase 3
Enrollment
120 people
Ages
18 years to 80 years
Study type
Interventional

Who can take part

  • You are between 18 and 80 years old.
  • You have been diagnosed with heterozygous familial hypercholesterolemia (a genetic condition causing very high cholesterol) by a doctor's criteria or genetic testing.
  • Your LDL ('bad') cholesterol is at least 2.6 mmol/L (about 100 mg/dL) at screening.
  • Your fasting triglycerides (a type of fat in the blood) are below 4.5 mmol/L.
  • If you take cholesterol-lowering medicines, your dose has been stable for at least 4 weeks and you are not planning to change it during the study.
  • Your kidney function is adequate (eGFR > 30 mL/min/1.73 m²).

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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