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

RecruitingPhase 4Ages 12 Years - anyAllAmryt Pharma
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In plain words

What the trial is, and whether it could suit you

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

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
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
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What it tests

  • Metreleptin
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Where

12 sites
Centre Hospitalier Régional Universitaire de Lille (CHRU) - Hôpital Claude Huriez
Lille, France
Hopital Pitie-Salpetriere
Paris, France
Hôpital Saint-Antoine
Paris, France
Centre Hospitalier Lyon-Sud
Pierre-Bénite, France
Charite-Universitaetsmedizin Berlin - Campus Charite Mitte (CCM)
Berlin, Germany
Universitaetsklinikum Ulm - Klinik fuer Kinder- und Jugendmedizin
Ulm, Germany
Azienda Ospedaliero-Universitaria di Bologna Policlinico S. Orsola-Malpighi
Bologna, Italy
Universitá degli Studi "Magna Graecia" di Catanzaro
Catanzaro, Italy

…and 4 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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