Abstract
Liraglutide (Saxenda®; 3 mg dose), a glucagon-like peptide-1 receptor agonist, is indicated as an adjunct to a reduced-calorie diet and increased physical activity for weight management in adult patients with an initial body mass index of ≥30 kg/m2 or ≥27 to <30 kg/m2 in the presence of at least one bodyweight-related co-morbidity (e.g. dysglycaemia, dyslipidaemia, hypertension, obstructive sleep apnoea). Clinical data in these patient populations indicates that subcutaneous liraglutide 3.0 mg once daily provides clinically meaningful (i.e. 5–10 % reduction) and sustained reductions in bodyweight and is generally well tolerated.
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Acknowledgments
The review was updated from Drugs 2015;75(8):899–910 [11], and was reviewed by: M. C. Mancini, Sao Paulo University, Endocrinology and Metabology Service, Obesity and Metabolic Syndrome Group, Sao Paulo, Brazil; J. L. Pérez-Castrillón, Rio Hortega University Hospital, University of Valladolid, Institute of Endocrinology and Nutrition, Valladolid, Spain; T. Tzotzas, Agios Pavlos General Hospital, Thessaloniki, Greece; W. M. Valencia, Geriatrics Research, Education and Clinical Center (GRECC) and Endocrine Section, Miami VA Medical Center, Miami, FL, USA. During the peer review process, the manufacturer of liraglutide was offered an opportunity to review this article. Changes resulting from comments received were made on the basis of scientific and editorial merit.
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The preparation of this review was not supported by any external funding.
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L. Scott is a salaried employee of Adis/Springer, is responsible for the article content and declares no relevant conflicts of interest.
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Scott, L.J. Liraglutide in obesity: a guide to its use in the EU. Drugs Ther Perspect 31, 334–340 (2015). https://doi.org/10.1007/s40267-015-0241-x
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DOI: https://doi.org/10.1007/s40267-015-0241-x