LOWER: Lomitapide Observational Worldwide Evaluation Registry

NCT02135705 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 260

Last updated 2026-05-12

No results posted yet for this study

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.

Conditions

  • Homozygous Familial Hypercholesterolemia

Interventions

DRUG

Lomitapide

As prescribed by Physician.

Sponsors & Collaborators

  • Amryt Pharma

    lead INDUSTRY

Principal Investigators

  • Janet Boylan · Amryt Pharmaceuticals

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-03-18
Primary Completion
2026-04-27
Completion
2026-04-27

Countries

  • United States
  • Argentina
  • Canada
  • France
  • Greece
  • Italy
  • Netherlands
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02135705 on ClinicalTrials.gov