Post Authorisation Safety Registry for US Patients With Generalised Lipodystrophy Treated With Metreleptin



Status:Not yet recruiting
Conditions:Endocrine
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:Any
Updated:4/2/2016
Start Date:January 2016
End Date:October 2029
Contact:AstraZeneca Clinical Study Information Center
Email:information.center@astrazeneca.com
Phone:1-877-240-9479

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Metreleptin Safety Registry

Post Authorisation Safety Registry for US patients with Generalised Lipodystrophy treated
with Metreleptin

Post Authorisation Safety Registry for US patients with Generalised Lipodystrophy treated
with Metreleptin.

This registry will add to the knowledge about metreleptin gained from clinical trials by
providing information on the incidence rates of acute pancreatitis, hypoglycemia,
hypersensitivity and lymphoma in patients treated with metreleptin in routine clinical
practice.

Inclusion Criteria:

- Patients who are treated with metreleptin as part of clinical care

- Patients who provide a written consent

Exclusion Criteria:

- Patient receiving metreleptin as part of a clinical trial or through expended access
including compassionate use

- Patients currently treated with an investigational agent as part of a clinical trial
We found this trial at
1
site
Staten Island, New York 10314
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mi
from
Staten Island, NY
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