RecruitingPhase 3NCT05682378
Long-term Safety and Tolerability of Inclisiran in Participants With HeFH or HoFH Who Have Completed the Adolescent ORION-16 or ORION-13 Studies
Studying Homozygous familial 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
- 195 enrolled
- Eligibility
- 12-100 years · All sexes
- Timeline
- 2023 – 2028
Study locations (30)
- Excel Medical Clinical Trials LLC, Boca Raton, Florida, United States
- Icahn School of Med at Mt Sinai, New York, New York, United States
- Cincinnati Childrens Hospital MC, Cincinnati, Ohio, United States
- Childrens Hosp Pittsburgh UPMC, Pittsburgh, Pennsylvania, United States
- Primary Childrens Medical Center, Salt Lake City, Utah, United States
- Novartis Investigative Site, Formosa, Formosa Province, Argentina
- Novartis Investigative Site, Fortaleza, Ceará, Brazil
- Novartis Investigative Site, São Paulo, São Paulo, Brazil
- Novartis Investigative Site, Québec, Quebec, Canada
- Novartis Investigative Site, Prague, Czechia
- Novartis Investigative Site, Besançon, France
- Novartis Investigative Site, Toulouse, France
- Novartis Investigative Site, Frankfurt am Main, Hesse, Germany
- Novartis Investigative Site, Freiburg im Breisgau, Germany
- Novartis Investigative Site, Athens, Greece
- +15 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 NCT05682378 on ClinicalTrials.govOther trials for Homozygous familial hypercholesterolemia
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