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MEASuRE: Metreleptin Effectiveness And Safety Registry

Launched by AEGERION PHARMACEUTICALS, INC. · Dec 22, 2014

Trial Information

Current as of November 01, 2025

Recruiting

Keywords

Lipodystrophy Metreleptin Registry

ClinConnect Summary

The MEASuRE study is a clinical trial designed to collect information on the effectiveness and safety of a medication called metreleptin, which is used to treat certain conditions related to lipodystrophy—this is when the body has trouble storing fat properly. The trial is open to patients who are already receiving metreleptin or have recently finished a clinical study and wish to continue the treatment. It aims to gather insights from patients across the U.S. and Europe who are using this medication.

To participate, individuals must be currently treated with metreleptin or have been treated in the past and be willing to provide written consent. However, those taking part in other clinical trials with experimental treatments cannot join this registry. Participants in the MEASuRE study can expect to provide information about their experiences with metreleptin, contributing to a better understanding of how this medication works in real-life settings. This is a voluntary registry, meaning patients can choose whether or not to take part.

Gender

ALL

Eligibility criteria

  • 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

About Aegerion Pharmaceuticals, Inc.

Aegerion Pharmaceuticals, Inc. is a biopharmaceutical company dedicated to developing and commercializing innovative therapies for rare genetic diseases, particularly those related to lipid metabolism disorders. With a strong focus on addressing unmet medical needs, Aegerion leverages cutting-edge research and advanced clinical development strategies to provide effective treatments for patients with conditions such as homozygous familial hypercholesterolemia. Committed to improving patient outcomes, Aegerion collaborates with healthcare professionals and patient advocacy groups to advance scientific knowledge and enhance the quality of life for individuals affected by these challenging disorders.

Locations

Ann Arbor, Michigan, United States

Ann Arbor, Michigan, United States

Philadelphia, Pennsylvania, United States

Philadelphia, Pennsylvania, United States

New Orleans, Louisiana, United States

New Orleans, Louisiana, United States

Duarte, California, United States

Seattle, Washington, United States

Dallas, Texas, United States

Detroit, Michigan, United States

Chicago, Illinois, United States

Paris, France

Paris, France

Cambridge, United Kingdom

Detroit, Michigan, United States

Roma, Italy

Kansas City, Kansas, United States

Atlanta, Georgia, United States

Muenster, Nordrhein Westfalen, Germany

Leipzig, Sachsen, Germany

Birmingham, Alabama, United States

Chicago, Illinois, United States

Kansas City, Kansas, United States

Bethesda, Maryland, United States

Staten Island, New York, United States

Columbus, Ohio, United States

Dallas, Texas, United States

Pisa, Italy

Ulm, Baden Wuerttemberg, Germany

Novara, Verceilli, Italy

Pisa, Italy

New Orleans, Louisiana, United States

Bethesda, Maryland, United States

Lille, Nord, France

Bologna, Italy

Paris, Paris, France, France

Hannover, Niedersachsen, Germany

Patients applied

0 patients applied

Trial Officials

Lori Hartnett

Study Director

Amryt Pharmaceuticals DAC

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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