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Completed Phase 2 Interventional Results available

A Study to Evaluate the Change in Weight After 24 Weeks Treatment With LIK066 in Obese or Overweight Adults

ClinicalTrials.gov ID: NCT03100058

Public ClinicalTrials.gov record NCT03100058. 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 19, 2026, 3:15 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

A Randomized, Double-blind, Dose-finding Study to Evaluate the Change in Weight After 24 Weeks Treatment With 8 Doses of LIK066 Compared to Placebo in Obese or Overweight Adults, Followed by 24 Weeks Treatment With 2 Doses of LIK066 and Placebo

Brief summary

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

This was a dose-finding study that evaluated the change in weight after 24 weeks treatment with 8 different doses of LIK066 compared to placebo in obese or overweight adults, followed by 24 weeks treatment with 2 doses of LIK066 and placebo.

Study identification

NCT ID
NCT03100058
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
460 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
May 6, 2017 (Actual)
Primary completion
Mar 2, 2018 (Actual)
Completion
Aug 2, 2018 (Actual)
Last update posted
Feb 6, 2020

2017 – 2018

United States locations

U.S. sites
59
U.S. states
24
U.S. cities
55
Facility City State ZIP Site status
Novartis Investigative Site Anniston Alabama 36207 —
Novartis Investigative Site Jasper Alabama 35501 —
Novartis Investigative Site Beverly Hills California 90211 —
Novartis Investigative Site Carmichael California 95608 —
Novartis Investigative Site Concord California 94520 —
Novartis Investigative Site Los Angeles California 90017 —
Novartis Investigative Site Northridge California 91325 —
Novartis Investigative Site Roseville California 95661 —
Novartis Investigative Site San Ramon California 94582 —
Novartis Investigative Site Stockton California 95204 —
Novartis Investigative Site Walnut Creek California 94598 —
Novartis Investigative Site Denver Colorado 80246 —
Novartis Investigative Site Golden Colorado 80401 —
Novartis Investigative Site Bradenton Florida 34209 —
Novartis Investigative Site Fort Lauderdale Florida 33312 —
Novartis Investigative Site Port Charlotte Florida 33952 —
Novartis Investigative Site West Palm Beach Florida 33401 —
Novartis Investigative Site Athens Georgia 30606 —
Novartis Investigative Site Augusta Georgia 30909 —
Novartis Investigative Site Honolulu Hawaii 96814 —
Novartis Investigative Site Gurnee Illinois 60031 —
Novartis Investigative Site Springfield Illinois 62711 —
Novartis Investigative Site Wauconda Illinois 60084 —
Novartis Investigative Site Evansville Indiana 47713 —
Novartis Investigative Site Evansville Indiana 47714 —
Novartis Investigative Site Indianapolis Indiana 46260 —
Novartis Investigative Site Louisville Kentucky 40213 —
Novartis Investigative Site Baton Rouge Louisiana 70808 —
Novartis Investigative Site Covington Louisiana 70433 —
Novartis Investigative Site Hammond Louisiana 70403 —
Novartis Investigative Site Metairie Louisiana 70006 —
Novartis Investigative Site New Orleans Louisiana 70115 —
Novartis Investigative Site New Orleans Louisiana 70119 —
Novartis Investigative Site Baltimore Maryland 21229 —
Novartis Investigative Site Beltsville Maryland 20705 —
Novartis Investigative Site Towson Maryland 21204 —
Novartis Investigative Site Royal Oak Michigan 48073 —
Novartis Investigative Site City of Saint Peters Missouri 63303 —
Novartis Investigative Site St Louis Missouri 63128 —
Novartis Investigative Site Missoula Montana 59808 —
Novartis Investigative Site Omaha Nebraska 68134 —
Novartis Investigative Site New York New York 10016 —
Novartis Investigative Site New York New York 10021 —
Novartis Investigative Site The Bronx New York 10455 —
Novartis Investigative Site Hickory North Carolina 28601 —
Novartis Investigative Site Lansdale Pennsylvania 19446 —
Novartis Investigative Site Pittsburgh Pennsylvania 15212 —
Novartis Investigative Site Moncks Corner South Carolina 29464 —
Novartis Investigative Site Mt. Pleasant South Carolina 29464 —
Novartis Investigative Site Summerville South Carolina 29485 —
Novartis Investigative Site Houston Texas 77081 —
Novartis Investigative Site Bountiful Utah 84010 —
Novartis Investigative Site Salt Lake City Utah 84102 —
Novartis Investigative Site Newport News Virginia 23606 —
Novartis Investigative Site Richmond Virginia 23235 —
Novartis Investigative Site Richmond Virginia 23294 —
Novartis Investigative Site Renton Washington 98057 —
Novartis Investigative Site Tacoma Washington 98405 —
Novartis Investigative Site Kenosha Wisconsin 53144 —

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03100058, 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 Feb 6, 2020 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03100058 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →