LOWER: Lomitapide Observational Worldwide Evaluation Registry

Study Identifier:
AEGR-733-025
ClinicalTrials.gov Identifier:
EudraCT Identifier:
N/A
EU CT ID:
N/A
Study Contact Information:
N/A
Study Complete

Study Details

Medical Condition
  • Homozygous Familial Hypercholesterolaemia (HoFH)
Study Drug
  • Drug: Lomitapide
Date
Mar 2014 - Apr 2026
Phase 1
Phase 2
Phase 3
Phase 4
N/A
Patient Requirements
Sex: Female & Male
Age: N/A
Requirements Information
Healthy Volunteers
No

Protocol Summary

This global product exposure registry is a multicentre, long-term, prospective, observational cohort study (exposure registry), designed to evaluate the long term safety and effectiveness of lomitapide.

Study Locations

Location
Status
Location
Brookwood Baptist Medical Center
Birmingham, Alabama, United States, 35209
Status
N/A
Location
Springhill Physician Practices
Mobile, Alabama, United States, 36608
Status
N/A
Location
Northern Arizona Healthcare
Cottonwood, Arizona, United States, 86326
Status
N/A
Location
Scottsdale Family Health
Phoenix, Arizona, United States, 85018
Status
N/A
Location
Pima Heart
Tucson, Arizona, United States, 85718
Status
N/A
Location
Arkansas Heart Center
Fort Smith, Arkansas, United States, 72901
Status
N/A
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