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2011 ADA Posters 1261-2041.indd - Diabetes

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placebo-controlled 56-week study. Subjects (N=1496) were randomized 2:1 to<br />

NB32 (32mg naltrexone SR/360mg bupropion SR) or placebo. The completion<br />

rate was 54% in each group. Baseline characteristics for the modifi ed ITT-<br />

LOCF population (subjects with ≥1 post-baseline weight on study drug) were:<br />

84% female, 85% Caucasian, mean±SD age 44±11y, weight 100±16kg, BMI<br />

36±4kg/m 2 , IWQOL-Lite Total score 73±17 (moderate impairment), IWQOL-<br />

Lite subscales: Physical Function 70.4±20.4, Self-Esteem 56.2±25.6, Sexual<br />

Life 75.5±26.3, Public Distress 86.6±18.0, Work 87.1±17.1, and SF-36:<br />

Physical Component 50.2±7.1 and Mental Component 54.4±7.3 (a score of 50<br />

is equivalent to average health). Week 56 weight loss was greater (p

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