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MEASuRE: Metreleptin Effectiveness And Safety Registry

Recruitingn/aAges any - anyAllChiesi Farmaceutici S.p.A.
NCT02325674 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The study is a post-authorization, prospective, voluntary registry of patients treated with commercial metreleptin including, but not limited to, patients in the US and EEA.

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

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patients treated with metreleptin through commercial supply at the time or before enrolment into registry * Patients who provide a written consent * Patient coming off metreleptin clinical studies and continuing or restarting treatment with metreleptin through commercial supply Exclusion Criteria: • Patients currently treated with an investigational agent as part of a clinical trial
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What it tests

  • Metreleptin
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Where

28 sites
University Alabama at Birmingham
Birmingham, United States
City of Hope
Duarte, United States
Atlanta Diabetes Associates
Atlanta, United States
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, United States
University of Kansas Medical Center Research Institute, Inc.
Kansas City, United States
Children's Hospital of New Orleans/LSU Health Sciences Center
New Orleans, United States
Ochsner Clinic Foundation
New Orleans, United States
Nih/Niddk/Deob
Bethesda, United States

…and 20 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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