A Multicenter, Double-blind, Randomized, Parallel-group, Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate-Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults

PHASE4CompletedINTERVENTIONAL
Enrollment

344

Participants

Timeline

Start Date

October 30, 2013

Primary Completion Date

August 31, 2014

Study Completion Date

September 3, 2014

Conditions
Chronic Weight Management
Interventions
DRUG

lorcaserin + phentermine placebo

lorcaserin 10 mg BID + phentermine placebo BID

DRUG

lorcaserin + phentermine-HCl + phentermine placebo

lorcaserin 10 mg BID + phentermine-HCl 15 mg QD + phentermine placebo QD

DRUG

lorcaserin + phentermine-HCl

lorcaserin 10 mg BID + phentermine-HCl 15 mg BID

Trial Locations (13)

10065

Weill Cornell College, New York

23294

National Clinical Research - Richmond, Richmond

23502

National Clinical Research - Norfolk, Norfolk

27710

Duke University, Durham

29621

Radiant Research - South Carolina, Anderson

32804

Translational Research Institute for Metabolism and Diabetes, Orlando

35294

University of Alabama at Birmingham, Birmingham

43212

Radiant Research - Columbus, Columbus

70808

Pennington Biomedical Research Center, Baton Rouge

75231

Radiant Research - Dallas, Dallas

85224

Radiant Research - Arizona, Chandler

92037

Scripps Clinical Research Center, La Jolla

Unknown

Boston Medical Center, Boston

All Listed Sponsors
lead

Eisai Inc.

INDUSTRY

NCT01987427 - A Multicenter, Double-blind, Randomized, Parallel-group, Pilot Study of 12-week Duration to Assess the Short-term Safety and Tolerability of Lorcaserin Plus Two Doses of Immediate-Release Phentermine-HCl Compared With Lorcaserin Alone in Overweight and Obese Adults | Biotech Hunter | Biotech Hunter