Clin2
NCT07473843Possibly a fitRecruiting

Study of zodasiran for teens with homozygous familial hypercholesterolemia

Homozygous Familial Hypercholesterolemia

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

This study tests an experimental medicine called zodasiran in teenagers who have a rare inherited condition that causes very high cholesterol. The goal is to see if it can lower cholesterol levels and reduce the risk of heart problems.

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

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

Who can take part

  • You are between 12 and 18 years old (not yet 18).
  • You weigh at least 35 kilograms (about 77 pounds).
  • You have a confirmed diagnosis of homozygous familial hypercholesterolemia (HoFH), either by genetic testing or clinical criteria.
  • Your LDL cholesterol (the 'bad' cholesterol) is at least 116 mg/dL at screening.
  • Your blood sugar (HbA1c) is 9.5% or lower.
  • Your liver function tests are within acceptable limits (bilirubin and enzymes).

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.

Similar studies

Other trials that look related to this one.

NCT07133815Not yet recruiting· Phase 2
Long-term safety study of SHR-1918 for familial hypercholesterolemia

This trial continues to test a drug called SHR-1918, which may help lower very high cholesterol in people with a genetic condition called homozygous familial hypercholesterolemia. It looks at whether the drug remains effective and safe over a longer period of time.

Changsha, Hunan
NCT06125847Recruiting· Early Phase 1
Gene therapy for inherited high cholesterol

This trial tests a one-time gene therapy to lower extremely high cholesterol in people with a rare inherited condition. It may help reduce heart attack risk in those who haven't responded to standard treatments.

Xi'an, Shaanxi
NCT06597006Recruiting· Phase 3
Study of inclisiran for children with homozygous familial high cholesterol

This trial tests a new medicine called inclisiran to lower very high cholesterol in children aged 2 to 12 who have a specific genetic condition (homozygous familial hypercholesterolemia, or HoFH). You may not need to change your current cholesterol treatments, and the study will check if inclisiran can help reduce your LDL cholesterol further.

San Francisco, California
NCT07489209Recruiting· Phase 2
Study of EDP167 for homozygous familial hypercholesterolemia

This trial tests a new drug, EDP167, for people with homozygous familial hypercholesterolemia (HoFH), a genetic condition that causes very high cholesterol. The goal is to see if EDP167 can lower 'bad' cholesterol (LDL-C).

Beijing
NCT06597019Recruiting· Phase 3
Study of inclisiran for children with high cholesterol

This trial tests a medicine called inclisiran to lower high cholesterol in children ages 6 to 12 with a genetic condition called heterozygous familial hypercholesterolemia (HeFH). It may help children who still have high cholesterol despite taking other treatments.

San Francisco, California
NCT07102511Enrolling by invitation· Phase 3
Testing a new cholesterol drug in children with high cholesterol

This trial tests if a new medicine, lerodalcibep, can safely lower cholesterol in children ages 6 to 17 who have a genetic condition called heterozygous familial hypercholesterolemia (HeFH). It aims to help children whose cholesterol stays high despite taking standard cholesterol-lowering drugs.

Cincinnati, Ohio

Hear when a new Homozygous Familial Hypercholesterolemia trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.