A One-Year Randomized Trial of Lorcaserin for Weight Loss in Obese and Overweight Adults: The BLOSSOM Trial

Author:

Fidler Meredith C.1,Sanchez Matilde1,Raether Brian1,Weissman Neil J.2,Smith Steven R.3,Shanahan William R.1,Anderson Christen M.1

Affiliation:

1. Arena Pharmaceuticals (M.C.F., M.S., B.R., W.R.S., C.M.A.), San Diego, California 92121

2. MedStar Health Research Institute at Washington Hospital Center and Georgetown University (N.J.W.), Washington, D.C. 20010

3. and Translational Research Institute for Metabolism and Diabetes (S.R.S.), Florida Hospital and the Sanford-Burnham Medical Research Institute, Orlando, Florida 32789

Abstract

Abstract Context: Lorcaserin is a novel selective agonist of the serotonin 2C receptor. Objective: Our objective was to evaluate the effects of lorcaserin on body weight, cardiovascular risk factors, and safety in obese and overweight patients. Design and Setting: This randomized, placebo-controlled, double-blind, parallel arm trial took place at 97 U.S. research centers. Patients: Patients included 4008 patients, aged 18–65 yr, with a body mass index between 30 and 45 kg/m2 or between 27 and 29.9 kg/m2 with an obesity-related comorbid condition. Interventions: Patients were randomly assigned in a 2:1:2 ratio to receive lorcaserin 10 mg twice daily (BID), lorcaserin 10 mg once daily (QD), or placebo. All patients received diet and exercise counseling. Main Outcome Measures: The ordered primary endpoints were proportion of patients achieving at least 5% reduction in body weight, mean change in body weight, and proportion of patients achieving at least 10% reduction in body weight at 1 yr. Serial echocardiograms monitored heart valve function. Results: Significantly more patients treated with lorcaserin 10 mg BID and QD lost at least 5% of baseline body weight (47.2 and 40.2%, respectively) as compared with placebo (25.0%, P < 0.001 vs. lorcaserin BID). Least squares mean (95% confidence interval) weight loss with lorcaserin BID and QD was 5.8% (5.5–6.2%) and 4.7% (4.3–5.2%), respectively, compared with 2.8% (2.5–3.2%) with placebo (P < 0.001 vs. lorcaserin BID; least squares mean difference, 3.0%). Weight loss of at least 10% was achieved by 22.6 and 17.4% of patients receiving lorcaserin 10 mg BID and QD, respectively, and 9.7% of patients in the placebo group (P < 0.001 vs. lorcaserin BID). Headache, nausea, and dizziness were the most common lorcaserin-related adverse events. U.S. Food and Drug Administration-defined echocardiographic valvulopathy occurred in 2.0% of patients on placebo and 2.0% on lorcaserin 10 mg BID. Conclusions: Lorcaserin administered in conjunction with a lifestyle modification program was associated with dose-dependent weight loss that was significantly greater than with placebo.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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