Evaluation of lorcaserin for the treatment of obesity

被引:11
作者
Berlie, Helen D. [1 ]
Hurren, Kathryn M. [2 ]
机构
[1] Wayne State Univ, Eugene Applebaum Coll Pharm & Hlth Sci, Dept Pharm Practice, Detroit, MI 48201 USA
[2] Vet Affairs Ann Arbor Healthcare Syst, Dept Ambulatory Care, Ann Arbor, MI 48105 USA
关键词
5-HT2C; belviq; lorcaserin; obesity; serotonin agonist; weight loss; MELANOCORTIN PATHWAYS; CONTROLLED-RELEASE; CONTROLLED-TRIAL; D-FENFLURAMINE; WEIGHT-LOSS; SEROTONIN; ADULTS; OVERWEIGHT; AGONIST; DEATHS;
D O I
10.1517/17425255.2013.798643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: Obesity is an epidemic associated with significant morbidity. Lorcaserin, a novel serotonin 2C receptor antagonist, was recently approved as an adjunct to lifestyle modification for long-term weight loss and maintenance. Clinical studies in patients without diabetes demonstrated 5.8% mean weight loss from baseline with lorcaserin compared to 2.5% with placebo and over twice as many patients achieved >= 5% weight loss. Patients with diabetes achieved mean weight loss of 4.5% with lorcaserin compared to 1.5% with placebo as well as modest improvements in glycemic outcomes. Areas covered: The authors review the pharmacology and clinical efficacy as well as the safety and tolerability of lorcaserin. This was achieved through a PubMed search (1960 - present) on lorcaserin to generate the key literature in the area. The lorcaserin package insert and Food and Drug Administration briefing documents were also used to identify relevant information. To assess long-term clinical efficacy and safety, the authors used studies with a minimum duration of one year. Expert opinion: Lorcaserin induces moderate but significant weight loss compared to placebo as an adjunct to lifestyle modification. Although head-to-head comparison trials are not available, lorcaserin is likely less effective but better tolerated than its recently approved competitor, phentermine/topiramate. Cardiovascular outcome data will be invaluable in determining lorcaserin's eventual utilization and place in therapy.
引用
收藏
页码:1053 / 1059
页数:7
相关论文
共 37 条
[1]   Controlled-Release Phentermine/Topiramate in Severely Obese Adults: A Randomized Controlled Trial (EQUIP) [J].
Allison, David B. ;
Gadde, Kishore M. ;
Garvey, William Timothy ;
Peterson, Craig A. ;
Schwiers, Michael L. ;
Najarian, Thomas ;
Tam, Peter Y. ;
Troupin, Barbara ;
Day, Wesley W. .
OBESITY, 2012, 20 (02) :330-342
[2]   Annual deaths attributable to obesity in the United States [J].
Allison, DB ;
Fontaine, KR ;
Manson, JE ;
Stevens, J ;
VanItallie, TB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (16) :1530-1538
[3]  
[Anonymous], 2013, QSYMIA
[4]  
[Anonymous], 2012, SCHED CONTR SUBST PL
[5]  
[Anonymous], 2012, XENICAL
[6]  
Centers for Disease Control and Prevention, 2012, CDC WEIGHT NAT PRESS
[7]   Pulmonary hypertension: therapeutic targets within the serotonin system [J].
Dempsie, Y. ;
MacLean, M. R. .
BRITISH JOURNAL OF PHARMACOLOGY, 2008, 155 (04) :455-462
[8]   A One-Year Randomized Trial of Lorcaserin for Weight Loss in Obese and Overweight Adults: The BLOSSOM Trial [J].
Fidler, Meredith C. ;
Sanchez, Matilde ;
Raether, Brian ;
Weissman, Neil J. ;
Smith, Steven R. ;
Shanahan, William R. ;
Anderson, Christen M. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (10) :3067-3077
[9]   Annual Medical Spending Attributable To Obesity: Payer- And Service-Specific Estimates [J].
Finkelstein, Eric A. ;
Trogdon, Justin G. ;
Cohen, Joel W. ;
Dietz, William .
HEALTH AFFAIRS, 2009, 28 (05) :W822-W831
[10]  
Fitzgerald LW, 2000, MOL PHARMACOL, V57, P75