drugset / Trial / NCT05164341

Study to Evaluate the Safety and Efficacy of Daily Subcutaneous Metreleptin Treatment in Subjects With PL

NCT05164341

Phase 3 Active not recruiting 69 enrolled Chiesi Farmaceutici S.p.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase III, double-blind, placebo-controlled, safety and efficacy study of daily SC metreleptin in subjects with Partial Lipodystrophy.

Timeline

Start
2021-12-17
Primary completion
2026-07-21
Completion
2026-10-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Metreleptin Protein / enzyme biologic Subcutaneous

Indications