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Open-label Study to Evaluate Metreleptin in Patients With Partial Lipodystrophy

Open-label Study to Evaluate Metreleptin in Patients With Partial Lipodystrophy

Recruiting
12 years and older
All
Phase 4
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Overview

This is an Open Label, Phase IV, Post Authorisation Study to Evaluate the Efficacy, Safety and Immunogenicity of Daily Subcutaneous Metreleptin Treatment in people with Partial Lipodystrophy

Eligibility

Inclusion Criteria:

  • Confirmed diagnosis of familial or acquired partial lipodystrophy

Exclusion Criteria:

  • Treatment with any Investigational Medicinal Product (IMP) within 6 months or 5 times the terminal half-life of the corresponding IMP, whichever is longer, before the screening visit.

Other protocol defined inclusion/exclusion criteria apply

Study details
    Partial Lipodystrophy

NCT06484868

Amryt Pharma

16 October 2025

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