RecruitingNCT02325674
MEASuRE: Metreleptin Effectiveness And Safety Registry
Sponsor
Amryt Pharma
Enrollment
100 participants
Start Date
Oct 11, 2016
Study Type
OBSERVATIONAL
Conditions
Summary
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.
Eligibility
Inclusion Criteria3
- 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 Criteria1
- • Patients currently treated with an investigational agent as part of a clinical trial
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Interventions
DRUGMetreleptin
Locations(28)
View Full Details on ClinicalTrials.gov
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NCT02325674