RecruitingPhase 3NCT06597006
Study to Evaluate Safety, Tolerability and Efficacy of Inclisiran in Children With Homozygous Familial Hypercholesterolemia
Studying Rare hypercholesterolemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Novartis Pharmaceuticals
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- Inclisiran(drug)
- Enrollment
- 9 enrolled
- Eligibility
- 2-11 years · All sexes
- Timeline
- 2025 – 2029
Study locations (17)
- UC San Francisco Medical Center, San Francisco, California, United States
- Childrens National Hospital, Washington D.C., District of Columbia, United States
- Washington Univ School Of Medicine, St Louis, Missouri, United States
- Novartis Investigative Site, Vienna, Austria
- Novartis Investigative Site, Beijing, Beijing Municipality, China
- Novartis Investigative Site, Frankfurt am Main, Hesse, Germany
- Novartis Investigative Site, Ioannina, Greece
- Novartis Investigative Site, Thessaloniki, Greece
- Novartis Investigative Site, Kota Bharu, Kelantan, Malaysia
- Novartis Investigative Site, Amsterdam, North Holland, Netherlands
- Novartis Investigative Site, Bloemfontein, Free State, South Africa
- Novartis Investigative Site, Taichung, Taiwan
- Novartis Investigative Site, Taipei, Taiwan
- Novartis Investigative Site, Adana, Saricam, Turkey (Türkiye)
- Novartis Investigative Site, Ankara, Yenimahalle, Turkey (Türkiye)
- +2 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT06597006 on ClinicalTrials.govOther trials for Rare hypercholesterolemia
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