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Heterozygous Familial Hypercholesterolaemia
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Heterozygous Familial Hypercholesterolaemia trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which Heterozygous Familial Hypercholesterolaemia trials may be worth asking aboutNorth America
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VT-10201 is an Open-label, Phase 1b, Single-ascending Dose Study That Will Evaluate the Safety of VERVE-102 Administered to Patients With Heterozygous Familial…
This study is designed to learn if enlicitide decanoate is safe and effective to treat children and adolescents with heterozygous familial hypercholesterolemia…
This multicenter, non-randomized interventional study aims to assess coronary artery disease progression over 5 years in patients with genetically confirmed het…
This is a single-arm, open-label, multicenter, ascending dose Phase 1 trial that will enroll participants 18 to 75 years of age with dyslipidemias that are refr…
The purpose of this open-label, single arm, multicenter extension study is to evaluate the long-term safety and tolerability of inclisiran in participants with…
This is a pivotal phase III study designed to evaluate safety, tolerability, and efficacy of inclisiran in children (aged 6 to \<12 years) with heterozygous fam…
The primary objective of this study is to determine the effect of once-daily oral MGL-3196 on the percent change from baseline in low-density lipoprotein choles…
This study aims to address several key questions regarding the use of inclisiran in real-world clinical practice in Spain.