MedTrace Logo

Setmelanotide for the Treatment of Leptin Receptor (LEPR) Deficiency Obesity

NCT03287960 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 15

Last updated 2023-05-23

Study results available
· View outcomes & findings →

Summary

To demonstrate statistically significant and clinically meaningful effects of setmelanotide on percent body weight change in participants with LEPR deficiency obesity due to rare bi-allelic or loss-of function mutations at the end of 1 year of treatment.

Conditions

  • Leptin Receptor Deficiency Obesity

Interventions

DRUG

Setmelanotide

Once daily subcutaneous injection

DRUG

Placebo

Once daily subcutaneous injection

Sponsors & Collaborators

  • Rhythm Pharmaceuticals, Inc.

    lead INDUSTRY

Principal Investigators

  • David Meeker, MD · Rhythm Pharmaceuticals, Inc.

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-30
Primary Completion
2020-09-25
Completion
2020-09-25
FDA Drug
Yes

Countries

  • Canada
  • France
  • Germany
  • Netherlands
  • Reunion
  • United Kingdom

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03287960 on ClinicalTrials.gov