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Naltrexone/Bupropion Extended Release-Induced Weight Loss Is Independent Of Nausea In Subjects Without Diabetes

Kurt Hong, K. Herrmann, C. Dybala,A. E. Halseth, H. Lam,J. P. Foreyt

CLINICAL OBESITY(2016)

Cited 9|Views15
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Abstract
Naltrexone/bupropion extended release (NB) is indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial body mass index of >= 30 or >= 27 kg m(-2) and >= 1 weight-related comorbidity (e.g. hypertension, type 2 diabetes and dyslipidaemia). In phase 3 clinical studies, nausea occurred in significantly higher proportions of subjects randomized to NB vs. placebo (PBO). In this pooled analysis of three phase 3, 56-week, PBO-controlled studies, we characterized nausea and weight loss in NB-and PBO-treated subjects without diabetes. Subjects receiving NB (n = 1778) lost significantly more weight than those receiving PBO (n = 1160). Weight change was not significantly different between subjects reporting and not reporting nausea in either treatment arm. Severity of nausea was mild to moderate in >= 95% of all cases. In the NB arm, the highest incidence of nausea onset (9%) was reported during week 1. The median duration of mild, moderate and severe nausea in subjects receiving NB was 14, 9 and 13 days, respectively. Our results demonstrate that nausea associated with NB is rarely severe, primarily occurs early in treatment and is not a contributor to weight loss.
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Key words
Adverse events, naltrexone/bupropion extended release, nausea, obesity
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