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NCT02654977 · ClinicalTrials.gov registry record · Phase 2

CLINICAL PROTOCOL to Investigate the Long-term Safety and Efficacy of Metreleptin in Various Forms of Partial Lipodystrophy

A Phase 2 study, sponsored by University of Michigan.

Completed
Registry status
Phase 2
Development phase
11
Enrollment target

NCT02654977: Completed Phase 2 study, sponsored by University of Michigan.

NCT02654977 is a Phase 2 study that has completed, run by University of Michigan. The registered enrollment target is 11 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02654977, a Phase 2 study, has completed, sponsored by University of Michigan.

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target

Study Summary

The study investigators' aim is to determine the long term safety and efficacy of Metreleptin (Myalept,) in promoting amelioration of metabolic abnormalities in patients with all forms of partial lipodystrophy. Patients will be offered this protocol under the following condition: Subjects have completed University of Michigan research protocol MB002-014 and have shown improved clinical benefit as judged by clinical criteria set forth in this protocol.

Primary Outcome

Fasting triglyceride levels after 5 years on metreleptin, measured in mg/dL are compared to fasting triglyceride levels at baseline). The median percent increase (positive numbers) or decrease from baseline is shown, along with the full range.

Interventions

  • DRUG Metreleptin

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2015-09-29
Est. Completion 2019-11-14
Phase Phase 2
University of Michigan

1,327 total trials

What the finished NCT02654977 record still lists

NCT02654977 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Metreleptin is the first listed.

NCT02654977 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02654977 about?

NCT02654977 is a clinical study titled "CLINICAL PROTOCOL to Investigate the Long-term Safety and Efficacy of Metreleptin in Various Forms of Partial Lipodystrophy". The study investigators' aim is to determine the long term safety and efficacy of Metreleptin (Myalept,) in promoting amelioration of metabolic abnormalities in patients with all forms of partial lipodystrophy. Patients will be offered this protocol under the following condition: Subjects have compl...

What is the current status of trial NCT02654977?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2015-09-29. Estimated completion is 2019-11-14.

What interventions are being tested in trial NCT02654977?

The interventions under investigation include: Metreleptin (DRUG).

Who is sponsoring clinical trial NCT02654977?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02654977's enrollment target sits among peer trials

11 1967th of 2000 higher than 33 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02654977, the US trial registry maintained by the National Library of Medicine. NCT02654977 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.