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Pharmacotherapy of Obesity: Clinical Trials to Clinical Practice.

Curr Diab Rep · 2017

Last updated 2026-05-28

Four FDA-approved drugs for long-term obesity treatment—lorcaserin, phentermine/topiramate, naltrexone/bupropion, and liraglutide 3.0 mg—show weight loss ranging from about 3% to 9% more than lifestyle changes alone after one year. Clinical trials found that some patients experienced significant benefits, while others saw modest or no improvements, and treatment choices should consider each patient’s balance of risks and benefits.

AI summary of the abstract below.

JournalCurr Diab Rep, 2017
Citations29
Relative citation ratio1.31
NIH percentile60
Molecules
Conditions studied Obesity

Abstract

PURPOSE OF REVIEW: This review provides an overview of the current state of drug therapy for obesity, with a focus on four new drug therapies-lorcaserin, phentermine/topiramate, naltrexone/bupropion, and liraglutide 3.0 mg-which have been approved by the US Food and Drug Administration (FDA) for long-term management of obesity since 2012. Topics discussed in this paper include rationale for pharmacotherapy, history of antiobesity drugs, and efficacy and safety data from randomized controlled trials with implications for clinical practice. RECENT FINDINGS: Weight loss achieved by currently approved drugs ranges from approximately 3 to 9%, above and beyond weight loss with lifestyle counseling alone, after a year. Response and attrition rates in clinical trials indicate that the benefits of pharmacotherapy range from substantial for some patients, modest for others, and no benefits for others still. Decisions regarding selection of a suitable drug from the available pharmacotherapy options and duration of treatment should be based on the expected and observed benefit-to-risk balance and tailored to the needs of each individual patient using the principles of shared decision-making.

Verbatim abstract via PubMed 28378293 ↗