Identifying and Genotyping Homozygous Familial Hypercholesterolemia (HoFH) Patients
NCT04148001 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4
Last updated 2021-02-02
Summary
This study is designed to help identify patients with HoFH due to mutations in the LDLR as confirmed by genotyping.
Conditions
- Homozygous Familial Hypercholesterolemia (HoFH)
Sponsors & Collaborators
- lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-12-04
- Primary Completion
- 2020-04-08
- Completion
- 2020-04-08
Countries
- United States
Study Locations
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