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Completed Phase 3 Interventional Results available

Effect of Liraglutide on Body Weight in Non-diabetic Obese Subjects or Overweight Subjects With Co-morbidities: SCALE™ - Obesity and Pre-diabetes

ClinicalTrials.gov ID: NCT01272219

Public ClinicalTrials.gov record NCT01272219. 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 30, 2026, 4:02 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

Effect of Liraglutide on Body Weight in Non-diabetic Obese Subjects or Overweight Subjects With Co-morbidities: A Randomised, Double-blind, Placebo Controlled, Parallel Group, Multi-centre, Multinational Trial With Stratification of Subject to Either 56 or 160 Weeks of Treatment Based on Pre-diabetes Status at Randomisation

Brief summary

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

This trial is conducted in Africa, Asia, Europe, Oceania, North America and South America. The aim of this clinical trial is to evaluate the potential of liraglutide to induce and maintain weight loss over 56 weeks in obese subjects or overweight subjects with co-morbidities. Furthermore, the aim is to investigate the long term potential of liraglutide to delay the onset of type 2 diabetes in subjects diagnosed with pre-diabetes at baseline. Based on body mass index (BMI) and pre-diabetes status, subjects will be randomised to either 68 weeks (56 weeks of randomised treatment followed by a 12 week re-randomised treatment period) or 160 weeks of treatment (160 week treatment will only be applicable to subjects with pre-diabetes status at baseline).

Study identification

NCT ID
NCT01272219
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
3,731 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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
Jun 1, 2011 (Actual)
Primary completion
Mar 18, 2013 (Actual)
Completion
Mar 2, 2015 (Actual)
Last update posted
Jan 19, 2018

2011 – 2015

United States locations

U.S. sites
73
U.S. states
27
U.S. cities
67
Facility City State ZIP Site status
Novo Nordisk Investigational Site Birmingham Alabama 35205-4731 —
Novo Nordisk Investigational Site Phoenix Arizona 85027 —
Novo Nordisk Investigational Site Anaheim California 92801 —
Novo Nordisk Investigational Site Concord California 94520 —
Novo Nordisk Investigational Site Huntington Beach California 92646 —
Novo Nordisk Investigational Site La Jolla California 92037 —
Novo Nordisk Investigational Site San Diego California 92103-4140 —
Novo Nordisk Investigational Site San Diego California 92108 —
Novo Nordisk Investigational Site Santa Monica California 90404 —
Novo Nordisk Investigational Site Aurora Colorado 80045 —
Novo Nordisk Investigational Site Colorado Springs Colorado 80904 —
Novo Nordisk Investigational Site Golden Colorado 80401 —
Novo Nordisk Investigational Site New London Connecticut 06320 —
Novo Nordisk Investigational Site Waterbury Connecticut 06708 —
Novo Nordisk Investigational Site Washington D.C. District of Columbia 20036-5847 —
Novo Nordisk Investigational Site Boynton Beach Florida 33437 —
Novo Nordisk Investigational Site Bradenton Florida 34201 —
Novo Nordisk Investigational Site Crystal River Florida 34429 —
Novo Nordisk Investigational Site Daytona Beach Florida 32117 —
Novo Nordisk Investigational Site Jacksonville Florida 32205 —
Novo Nordisk Investigational Site Jacksonville Florida 32216 —
Novo Nordisk Investigational Site Ocala Florida 34471 —
Novo Nordisk Investigational Site Ponte Vedra Florida 32081 —
Novo Nordisk Investigational Site South Miami Florida 33143 —
Novo Nordisk Investigational Site Athens Georgia 30606 —
Novo Nordisk Investigational Site Dunwoody Georgia 30338 —
Novo Nordisk Investigational Site Sandy Springs Georgia 30328 —
Novo Nordisk Investigational Site Suwanee Georgia 30024 —
Novo Nordisk Investigational Site Aurora Illinois 60504 —
Novo Nordisk Investigational Site Topeka Kansas 66606 —
Novo Nordisk Investigational Site Baton Rouge Louisiana 70808-4124 —
Novo Nordisk Investigational Site Baltimore Maryland 21209 —
Novo Nordisk Investigational Site Elkridge Maryland 21075-6437 —
Novo Nordisk Investigational Site North Dartmouth Massachusetts 02747 —
Novo Nordisk Investigational Site City of Saint Peters Missouri 63376 —
Novo Nordisk Investigational Site Kansas City Missouri 64111 —
Novo Nordisk Investigational Site St Louis Missouri 63104 —
Novo Nordisk Investigational Site St Louis Missouri 63141 —
Novo Nordisk Investigational Site New York New York 10025 —
Novo Nordisk Investigational Site Rochester New York 14609 —
Novo Nordisk Investigational Site Staten Island New York 10301 —
Novo Nordisk Investigational Site Syracuse New York 13210 —
Novo Nordisk Investigational Site Cary North Carolina 27518 —
Novo Nordisk Investigational Site Raleigh North Carolina 27612 —
Novo Nordisk Investigational Site Canal Fulton Ohio 44614 —
Novo Nordisk Investigational Site Cincinnati Ohio 45219 —
Novo Nordisk Investigational Site Franklin Ohio 45005 —
Novo Nordisk Investigational Site Wadsworth Ohio 44281-9236 —
Novo Nordisk Investigational Site Tulsa Oklahoma 74136 —
Novo Nordisk Investigational Site Eugene Oregon 97401 —
Novo Nordisk Investigational Site Beaver Pennsylvania 15009 —
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19107 —
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15206 —
Novo Nordisk Investigational Site West Reading Pennsylvania 19611 —
Novo Nordisk Investigational Site Charleston South Carolina 29425 —
Novo Nordisk Investigational Site Greer South Carolina 29651 —
Novo Nordisk Investigational Site Bristol Tennessee 37620-7352 —
Novo Nordisk Investigational Site Austin Texas 78731 —
Novo Nordisk Investigational Site Dallas Texas 75231 —
Novo Nordisk Investigational Site Dallas Texas 75234 —
Novo Nordisk Investigational Site Dallas Texas 75251 —
Novo Nordisk Investigational Site Dallas Texas 75390-8858 —
Novo Nordisk Investigational Site San Antonio Texas 78229-4801 —
Novo Nordisk Investigational Site Sugar Land Texas 77479 —
Novo Nordisk Investigational Site Salt Lake City Utah 84107 —
Novo Nordisk Investigational Site West Jordan Utah 84088-8871 —
Novo Nordisk Investigational Site Arlington Virginia 22206 —
Novo Nordisk Investigational Site Henrico Virginia 23233 —
Novo Nordisk Investigational Site Richmond Virginia 23294 —
Novo Nordisk Investigational Site Virginia Beach Virginia 23454 —
Novo Nordisk Investigational Site Renton Washington 98057 —
Novo Nordisk Investigational Site Wenatchee Washington 98801-2028 —
Novo Nordisk Investigational Site Milwaukee Wisconsin 53209 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 153 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01272219, 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 19, 2018 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01272219 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →