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Terminated Phase 4 Interventional Accepts healthy volunteers Results available

Study to Evaluate the Efficacy and Safety of Belviq XR® in Conjunction With Lifestyle Modification for Weight Loss in Obese Adolescents, Age 12 to 17 Years

ClinicalTrials.gov ID: NCT03338296

Public ClinicalTrials.gov record NCT03338296. 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 Jul 22, 2026, 11:45 AM 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 52 Week Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Belviq XR® in Conjunction With Lifestyle Modification for Weight Loss in Obese Adolescents, Age 12 to 17 Years

Study identification

NCT ID
NCT03338296
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Eisai Inc.
Industry
Enrollment
278 participants

Conditions and interventions

Conditions

Interventions

  • lorcaserin hydrochloride XR Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
12 Years to 17 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 27, 2017
Primary completion
Apr 2, 2020
Completion
Apr 2, 2020
Last update posted
Jul 18, 2021

2017 – 2020

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Phoenix Clinical LLC Phoenix Arizona 85014
Alliance Research Institute Bell Gardens California 90201
Long Beach Clinical Trial Services, Inc Long Beach California 90806
International Research Partners LLC Doral Florida 33122
Oviedo Medical Research, LLC Oviedo Florida 32765
Gwinnett Research Institute Buford Georgia 30519
Columbus Regional Research Institute Columbus Georgia 31904
Buynak Clinical Research, PC Valparaiso Indiana 46383
Heartland Research Associates, LLC Wichita Kansas 67207
The Center for Pharmaceutical Research, LLC Kansas City Missouri 64114
Wake Research-Clinical Research Center of Nevada, LLC Henderson Nevada 89014
Diabetes & Endocrinology Consultants, PC Morehead City North Carolina 28557
Neuro-Behavioral Clinical Research, Inc North Canton Ohio 44720
Celia Reyes-Acuna, MD Corpus Christi Texas 78413
DCT-McAllen Primary Care, LLC dba Discovery Clinical Trials McAllen Texas 78503
National Clinical Research-Richmond, Inc Richmond Virginia 23294

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03338296, 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 Jul 18, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03338296 live on ClinicalTrials.gov.

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