Evaluation of Safety and Efficiency of Metreleptin Treatment for Patients With Multiple Symmetric Lipomatosis (MSL)

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

4

Participants

Timeline

Start Date

August 1, 2023

Primary Completion Date

April 8, 2024

Study Completion Date

October 31, 2028

Conditions
Lipomatosis, Multiple Symmetrical
Interventions
DRUG

Metreleptin

Study drug for injection is supplied in a carton containing 30 vials for reconstitution. Each vial contains 11.3 mg of the study drug as a sterile, white, solid, lyophilized cake or powder to deliver 5 mg/mL of the study drug when reconstituted with 2.2 mL of water for injection (WFI).

Trial Locations (1)

48109

University of Michigan, Ann Arbor

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Amryt Pharma

INDUSTRY

lead

University of Michigan

OTHER