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1 ents with SBS-IF who were given subcutaneous teduglutide (0.05 mg/kg/d; n = 43) or placebo (n = 43) o
2 , 14 women) to receive subcutaneous doses of teduglutide 4 mg or placebo (2:1 ratio; 23:13) once dail
7 with SBS support the safety and efficacy of teduglutide as an aid to parenteral nutrition weaning.
8 ed for parenteral support was greater in the teduglutide group (21/39 [54%]) than in the placebo grou
9 re were significantly more responders in the teduglutide group (27/43 [63%]) than the placebo group (
10 eduction in parenteral support volume in the teduglutide group was 4.4 +/- 3.8 L/wk (baseline 12.9 +/
12 identify characteristics of patients in whom teduglutide has the largest effects on parenteral suppor
13 The effects of mitogenic stimulation with teduglutide in patients with short bowel syndrome might
19 the intestinal mucosa, and a GLP-2R agonist, teduglutide, is now used for augmentation of energy abso
22 ve of this study was to assess the effect of teduglutide on gastric emptying of liquids in healthy su
24 ata from a phase III study of the effects of teduglutide on patients with SBS, we associated reduced
25 tabolism classification system, who received teduglutide or placebo between November 25, 2008, and Ja
29 med a prospective study to determine whether teduglutide reduces parenteral support in patients with
30 BACKGROUND & AIMS: Clinical studies showed teduglutide to increase urine production and reduce need
31 ndrome might be greater if the more numerous teduglutide-treated cells could be stimulated toward a m
32 436 mL/d; P = .0112) but also compared with teduglutide-treated patients in group 2 (reduction of 35
33 ted parenteral support volume reduction with teduglutide treatment and baseline parenteral support vo
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