{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T10:00:26Z","timestamp":1790330426233,"version":"4.1.0"},"reference-count":40,"publisher":"The Endocrine Society","issue":"10","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,10,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Context:<\/jats:title>\n                    <jats:p>Lorcaserin is a novel selective agonist of the serotonin 2C receptor.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective:<\/jats:title>\n                    <jats:p>Our objective was to evaluate the effects of lorcaserin on body weight, cardiovascular risk factors, and safety in obese and overweight patients.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design and Setting:<\/jats:title>\n                    <jats:p>This randomized, placebo-controlled, double-blind, parallel arm trial took place at 97 U.S. research centers.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Patients:<\/jats:title>\n                    <jats:p>Patients included 4008 patients, aged 18\u201365 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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Interventions:<\/jats:title>\n                    <jats:p>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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Main Outcome Measures:<\/jats:title>\n                    <jats:p>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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>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 &amp;lt; 0.001 vs. lorcaserin BID). Least squares mean (95% confidence interval) weight loss with lorcaserin BID and QD was 5.8% (5.5\u20136.2%) and 4.7% (4.3\u20135.2%), respectively, compared with 2.8% (2.5\u20133.2%) with placebo (P &amp;lt; 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 &amp;lt; 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.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions:<\/jats:title>\n                    <jats:p>Lorcaserin administered in conjunction with a lifestyle modification program was associated with dose-dependent weight loss that was significantly greater than with placebo.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1210\/jc.2011-1256","type":"journal-article","created":{"date-parts":[[2011,7,27]],"date-time":"2011-07-27T23:56:10Z","timestamp":1311810970000},"page":"3067-3077","source":"Crossref","is-referenced-by-count":454,"title":["A One-Year Randomized Trial of Lorcaserin for Weight Loss in Obese and Overweight Adults: The BLOSSOM Trial"],"prefix":"10.1210","volume":"96","author":[{"given":"Meredith C.","family":"Fidler","sequence":"first","affiliation":[{"name":"Arena Pharmaceuticals (M.C.F., M.S., B.R., W.R.S., C.M.A.), San Diego, California 92121"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matilde","family":"Sanchez","sequence":"additional","affiliation":[{"name":"Arena Pharmaceuticals (M.C.F., M.S., B.R., W.R.S., C.M.A.), San Diego, California 92121"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brian","family":"Raether","sequence":"additional","affiliation":[{"name":"Arena Pharmaceuticals (M.C.F., M.S., B.R., W.R.S., C.M.A.), San Diego, California 92121"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Neil J.","family":"Weissman","sequence":"additional","affiliation":[{"name":"MedStar Health Research Institute at Washington Hospital Center and Georgetown University (N.J.W.), Washington, D.C. 20010"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Steven R.","family":"Smith","sequence":"additional","affiliation":[{"name":"and Translational Research Institute for Metabolism and Diabetes (S.R.S.), Florida Hospital and the Sanford-Burnham Medical Research Institute, Orlando, Florida 32789"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"William R.","family":"Shanahan","sequence":"additional","affiliation":[{"name":"Arena Pharmaceuticals (M.C.F., M.S., B.R., W.R.S., C.M.A.), San Diego, California 92121"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christen M.","family":"Anderson","sequence":"additional","affiliation":[{"name":"Arena Pharmaceuticals (M.C.F., M.S., B.R., W.R.S., C.M.A.), San Diego, California 92121"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"80","reference":[{"key":"2020071616062322300_B1","article-title":"Fact sheet: obesity and overweight. 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