MEASuRE: Metreleptin Effectiveness And Safety Registry
Launched by AEGERION PHARMACEUTICALS, INC. · Dec 22, 2014
Trial Information
Current as of November 01, 2025
Recruiting
Keywords
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Trial Officials
Lori Hartnett
Study Director
Amryt Pharmaceuticals DAC
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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