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

Completed · Phase 3 · NCT05164341

Conditions: Partial Lipodystrophy

At a glance

Research payments reported, 2025
$591,275
U.S. investigators named
12
Sites paid
12
Planned or actual enrollment
69

About the trial

Sponsor
Chiesi Farmaceutici S.p.A.
Tested
metreleptin (drug), Placebo (drug)
Dates
Started 2021-12-17; completion 2026-10-06
Results posted
Not yet

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

From ClinicalTrials.gov, last updated 2026-11-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Chiesi USA, Inc. reported $591,275 in research payments for this study in 2025 (351 payments).

Products named: Myalept

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.