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Clinical trial

A 24-Month, Multi-Centre, Open Label Phase IV Post Authorisation Efficacy Study to Evaluate the Efficacy, Safety and Immunogenicity of Daily Subcutaneous Metreleptin Treatment in Patients With Partial Lipodystrophy

NCT06484868 is registered in ClinicalTrials.gov with Amryt Pharma as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A 24-Month, Multi-Centre, Open Label Phase IV Post Authorisation Efficacy Study to Evaluate the Efficacy, Safety and Immunogenicity of Daily Subcutaneous Metreleptin Treatment in Patients With Partial Lipodystrophy
Lead sponsor
Amryt Pharma
Phase
Phase 4
Overall status
Recruiting
Start date
February 8, 2024
Completion date
February 29, 2028
Enrollment
12 (estimated)
Sites
12

Conditions

As the registry lists them; a condition with its own page is linked.

partial lipodystrophy