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