Two-year sustained weight loss and metabolic benefits with controlled-release phentermine/topiramate in obese and overweight adults (SEQUEL): a randomized, placebo-controlled, phase 3 extension study

被引:453
作者
Garvey, W. Timothy [1 ,2 ,3 ]
Ryan, Donna H. [4 ]
Look, Michelle [5 ]
Gadde, Kishore M. [6 ]
Allison, David B. [7 ]
Peterson, Craig A. [8 ]
Schwiers, Michael [9 ]
Day, Wesley W. [8 ]
Bowden, Charles H. [8 ]
机构
[1] Univ Alabama Birmingham, Dept Nutr Sci, UAB Diabet Res & Training Ctr, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Med, UAB Diabet Res & Training Ctr, Birmingham, AL 35294 USA
[3] Birmingham VA Med Ctr, Birmingham, AL USA
[4] Pennington Biomed Res Ctr, Baton Rouge, LA USA
[5] San Diego Sports Med, San Diego, CA USA
[6] Duke Univ, Med Ctr, Obes Clin Trials Program, Durham, NC USA
[7] Univ Alabama Birmingham, Dept Biostat, UAB Nutr & Obes Res Ctr, Birmingham, AL 35294 USA
[8] Vivus Inc, Mountain View, CA USA
[9] Medpace, Cincinnati, OH USA
关键词
DOUBLE-BLIND; TOPIRAMATE; EFFICACY; SAFETY; COMBINATION; MANAGEMENT;
D O I
10.3945/ajcn.111.024927
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Obesity is a serious chronic disease. Controlled-release phentermine/topiramate (PHEN/TPM CR), as an adjunct to lifestyle modification, has previously shown significant weight loss compared with placebo in a 56-wk study in overweight and obese subjects with >= 2 weight-related comorbidities. Objective: This study evaluated the long-term efficacy and safety of PHEN/TPM CR in overweight and obese subjects with cardiometabolic disease. Design: This was a placebo-controlled, double-blind, 52-wk extension study; volunteers at selected sites continued with original randomly assigned treatment [placebo, 7.5 mg phentermine/46 mg controlled-release topiramate (7.5/46), or 15 mg phentermine/92 mg controlled-release topiramate (15/92)] to complete a total of 108 wk. All subjects participated in a lifestyle-modification program. Results: Of 866 eligible subjects, 676 (78%) elected to continue in the extension. Overall, 84.0% of subjects completed the study, with similar completion rates between treatment groups. At week 108, PHEN/TPM CR was associated with significant, sustained weight loss (intent-to-treat with last observation carried forward; P < 0.0001 compared with placebo); least-squares mean percentage changes from baseline in body weight were -1.8%, -9.3%, and -10.5% for placebo, 7.5/46, and 15/92, respectively. Significantly more PHEN/TPM CR-treated subjects at each close achieved >= 5%, >= 10%, >= 15%, and >= 20% weight loss compared with placebo (P < 0.001). PHEN/TPM CR improved cardiovascular and metabolic variables and decreased rates of incident diabetes in comparison with placebo. PHEN/TPM CR was well tolerated over 108 wk, with reduced rates of adverse events occurring between weeks 56 and 108 compared with rates between weeks 0 and 56. Conclusion: PHEN/TPM CR in conjunction with lifestyle modification may provide a well-tolerated and effective option for the sustained treatment of obesity complicated by cardiometabolic disease. This trial was registered at clinicaltrials.gov as NCT00796367. Am J Clin Nutr 2012;95:297-308.
引用
收藏
页码:297 / 308
页数:12
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