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NCT05093634CompletedPhase 3

EMANATE: A Study of Setmelanotide in Patients With Specific Gene Variants in the MC4R Pathway

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Trial: Multiple Independent Sub-studies of Setmelanotide in Patients With POMC/PCSK1, LEPR, NCOA1(SRC1), or SH2B1 Gene Variants in the Melanocortin-4 Receptor Pathway

Source: ClinicalTrials.gov · Last updated 6 Aug 2026

Brief summary (registry, in English)

The protocol describes a randomized, double-blind, placebo-controlled trial with independent sub-studies of setmelanotide in patients with obesity and at least one of the specific gene variants in the Melanocortin-4 Receptor pathway: * POMC or PCSK1 (Sub-study 035a) * LEPR (Sub-study 035b) * SRC1 (Sub-study 035c) * SH2B1 (Sub-study 035d) The objectives and endpoints are identical for these sub-studies.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
296 (actual)
First submitted
30 Sept 2021
Start date
10 Dec 2021
Primary completion date
22 Dec 2025
Lead sponsor
Rhythm Pharmaceuticals, Inc.
Diseases
Obesity
NCT number
NCT05093634

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 296
  • From 10 Dec 2021 to the primary completion date, 22 Dec 2025
  • 56 sites in 10 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Weight loss of 2% or greater in the previous 3 months
  • Participation in any clinical study with an investigational drug/device within 3 months prior to the first day of dosing
  • Previously enrolled in a clinical study involving setmelanotide or any previous exposure to setmelanotide

Other illness

  • Recent history of bariatric surgery
  • Significant psychiatric disorder(s)
  • Clinically significant pulmonary, cardiac, endocrine/metabolic, hepatic or oncologic disease
  • History of significant liver disease or severe kidney disease
  • History or close family history (parents or siblings) of melanoma, or patient history of oculocutaneous albinism
  • Significant hypersensitivity to any excipient in the study drug

Lab values

  • Glycated hemoglobin (HbA1C) \>10% at Screening

Other

  • Suicidal ideation, attempt or behavior
  • Significant dermatologic findings relating to melanoma or pre-melanoma skin lesions (excluding non-invasive basal or squamous cell lesion)
  • If female, pregnant or breastfeeding

Who the study is looking for

  • Patients must have a pre-identified:
    • Heterozygous genetic variant in the POMC gene or PCSK1 gene
    • Heterozygous genetic variant in the LEPR gene
    • Homozygous, heterozygous, or compound heterozygous variant in the NCOA1 (SRC1)
    • Homozygous, heterozygous, or compound heterozygous variant in SH2B1 gene, or chromosomal 16p11.2 deletion encompassing the SH2B1 gene
  • Between 6 and 65 years of age at the time of provision of informed consent/assent
  • Obesity, defined as BMI ≥30 kg/m2 for patients ≥18 years of age or BMI ≥95th percentile for age and gender for patients 6 up to 17 years of age
  • Patient and/or parent or guardian is able to understand and comply with the requirements of the study and is able to understand and sign the written informed consent/assent
  • Patient and/or parent or guardian reports that patient experienced childhood obesity, defined as the patient and/or parent or guardian reporting that the patient was significantly overweight during childhood
  • Agree to use a highly effective form of contraception throughout the study and for 90 days following the study
  • Reported history of lifestyle intervention of diet and exercise
  • Reported history of hyperphagia

Age in the registry: 6 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (56)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alberta - Alberta Diabetes Institute (ADI)
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EdmontonCanadaUnknown status
Charité Universitätsmedizin Berlin
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BerlinGermanyUnknown status
Endokrinologikum Frankfurt
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FrankfurtGermanyUnknown status
Universitaetsklinikum Leipzig
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LeipzigGermanyUnknown status
Universitaetsklinikum Ulm
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UlmGermanyUnknown status
Hospital Sant Joan de Déu Barcelona
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BarcelonaSpainUnknown status
Hospital Fundación Jimenez Diaz
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MadridSpainUnknown status
Hospital Universitario Virgen de la Victoria de Málaga
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MálagaSpainUnknown status
Hospital General de Valencia
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ValenciaSpainUnknown status
GH Est Hopital Femme Mere Enfant
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LyonFranceUnknown status
Hôpital Armand-Trousseau
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ParisFranceUnknown status
Hu Pitie Salpetriere Aphp
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ParisFranceUnknown status
Centre Hospitalier Universitaire (CHU) de Bordeaux
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PessacFranceUnknown status
Hôpital Félix Guyon Bellepierre
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Saint-DenisFranceUnknown status
Bristol Royal Hospital for Children
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BristolUnited KingdomUnknown status
University of Cambridge
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CambridgeUnited KingdomUnknown status
Aintree University Hospital
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LiverpoolUnited KingdomUnknown status
London Medical - The London Diabetes Centre
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LondonUnited KingdomUnknown status
University College London Hospitals NHS Foundation Trust
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LondonUnited KingdomUnknown status
University of Patras School of Medicine
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RioGreeceUnknown status
Hasharon Hospital
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Petah TikvaIsraelUnknown status
Chaim Sheba MC, Safra Children's Hospital
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Ramat GanIsraelUnknown status
Erasmus Medisch Centrum
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RotterdamNetherlandsUnknown status
University of Puerto Rico
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San JuanPuerto RicoUnknown status
Advent Health
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Altamonte SpringsUnited StatesUnknown status
Texas Tech
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AmarilloUnited StatesUnknown status
University of Michigan
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Ann ArborUnited StatesUnknown status
Children's Hospital Colorado
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AuroraUnited StatesUnknown status
University of Buffalo
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BuffaloUnited StatesUnknown status
St. Luke's Hospital
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ChesterfieldUnited StatesUnknown status
Cincinnati Children's Hospital Medical Center
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CincinnatiUnited StatesUnknown status
Geisinger Clinic
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DanvilleUnited StatesUnknown status
Metro Detroit Endocrinology Center
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DearbornUnited StatesUnknown status
Texas Children's Hospital
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HoustonUnited StatesUnknown status
Biopharma Informatic
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HoustonUnited StatesUnknown status
Children's Hospital Los Angeles
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Los AngelesUnited StatesUnknown status
Marshfield Clinic Research Foundation, a Division of Marshfield Clinic, Inc
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MarshfieldUnited StatesUnknown status
Rio Grande Valley Endocrine Center
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McAllenUnited StatesUnknown status
West Virginia University
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MorgantownUnited StatesUnknown status
Vanderbilt University School of Medicine
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NashvilleUnited StatesUnknown status
Yale Center for Clinical Investigation
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New HavenUnited StatesUnknown status
Metropolitan Hospital Center
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New YorkUnited StatesUnknown status
Mount Sinai Hospital
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New YorkUnited StatesUnknown status
Columbia University
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New YorkUnited StatesUnknown status
Children's Hospital of Philadelphia
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PhiladelphiaUnited StatesUnknown status
Phoenix Children s Hospital
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PhoenixUnited StatesUnknown status
UPMC Montefiore
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PittsburghUnited StatesUnknown status
Endocrine Associates of Dallas and Plano
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PlanoUnited StatesUnknown status
Oregon Health Science University
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PortlandUnited StatesUnknown status
Mayo Clinic
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RochesterUnited StatesUnknown status
HonorHealth Bariatric Center
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ScottsdaleUnited StatesUnknown status
Ten's Medical Center - Pediatric Endocrinology Clinic
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Staten IslandUnited StatesUnknown status
Washington University in St. Louis
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St LouisUnited StatesUnknown status
InQuest Medical Research
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SuwaneeUnited StatesUnknown status
MultiCare Health System Institute for Research and Innovation
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TacomaUnited StatesUnknown status
Umass Memorial Medical Center
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WorcesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.