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BLOSSOM: Behavioral Modification and Lorcaserin Second Study for Obesity Management

NCT00603902 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 4008

Last updated 2019-10-04

Study results available
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Summary

The purpose of this study is to assess the weight loss effect of lorcaserin during and at the end of 1 year of treatment in overweight and obese patients.

Conditions

Interventions

DRUG

Lorcaserin 10 mg once daily (QD)

Lorcaserin 10 mg tablet each morning and placebo tablet each evening for a duration of 52 weeks.

DRUG

Lorcaserin 10 mg twice a day (BID)

Lorcaserin 10 mg tablet each morning and evening for a duration of 52 weeks.

DRUG

Matching Placebo

Matching placebo tablet each morning and evening for a duration of 52 weeks.

Sponsors & Collaborators

  • Eisai Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2009-07-31
Completion
2009-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00603902 on ClinicalTrials.gov