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Terminated Phase 3 Interventional

Double-Blind, Placebo Controlled, Phase 3 Trial of ZGN-440 (Beloranib) in Obese Subjects With Prader-Willi Syndrome

ClinicalTrials.gov ID: NCT02179151

Public ClinicalTrials.gov record NCT02179151. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 10:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized, Double-Blind, Placebo Controlled, Phase 3 Trial of ZGN-440 (Subcutaneous Beloranib in Suspension) in Obese Subjects With Prader-Willi Syndrome to Evaluate Total Body Weight, Food-related Behavior, and Safety Over 6 Months

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate efficacy and safety of ZGN-440 (beloranib) in obese adolescent and adult subjects with Prader-Willi Syndrome.

Study identification

NCT ID
NCT02179151
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Zafgen, Inc.
Industry
Enrollment
108 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2014 (Type not available)
Primary completion
Dec 2015 (Actual)
Completion
Oct 2016 (Actual)
Last update posted
Jan 26, 2017

2014 – 2016

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
University of California, Davis Sacramento California 95817 —
UCSD: Rady Children's Hospital San Diego California 92123 —
Children's Hospital of Colorado Aurora Colorado 80045 —
University of Florida Gainesville Florida 32610 —
Kansas University Medical Center Kansas City Kansas 66160 —
National Institute of Child Health Bethesda Maryland 20892 —
Children's Hospital Boston Boston Massachusetts 02115 —
Children's Hospital and Clinics of Minnesota Saint Paul Minnesota 55102 —
Saint Louis University St Louis Missouri 63104 —
Winthrop University Mineola New York 11501 —
University Hospitals Case Medical Center Cleveland Ohio 44106 —
Vanderbilt University Nashville Tennessee 37235 —
Texas Children's Hospital Houston Texas 77030 —
University of Utah Salt Lake City Utah 84112 —
Seattle Children's Research Institute Seattle Washington 98105 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02179151, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 26, 2017 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02179151 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →