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NCT02849977

Genetic Testing and Phenotypic Characterization of Severely Obese Pediatric and Adult Volunteers

Completed Last updated 15 November 2022
What this trial tests

trial in Pro-opiomelanocortin (POMC), Proprotein Convertase Subtilisin/Kexin Type 1 (PCSK1) and Leptin Receptor (LepR) Gene Mutations in 5,966 participants. Completed in 9 June 2020.

Timeline
28 September 2016
Primary endpoint
9 June 2020
9 June 2020

Quick facts

Lead sponsorRhythm Pharmaceuticals, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment5,966
Start date28 September 2016
Primary completion9 June 2020
Estimated completion9 June 2020
Sites58 locations across Italy, Greece, Israel, Germany, Canada, Portugal, United States

Conditions studied

Sponsor

Rhythm Pharmaceuticals, Inc. — full company profile →

Who can join

2 and older, any sex, with Pro-opiomelanocortin (POMC), Proprotein Convertase Subtilisin/Kexin Type 1 (PCSK1) and Leptin Receptor (LepR) Gene Mutations. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this screening study is to identify people who have a rare genetic cause of obesity - specifically three genetic variants (a change in the DNA structure) of the POMC, PCSK1 and LepR genes that are currently known to result in obesity. This screening study will not include any investigational drugs. You will be asked to provide a DNA sample and answer some questions about your medical history and hunger.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Rhythm Pharmaceuticals, Inc. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02849977.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing