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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
3 ere observed on Day 10 in subjects receiving teduglutide 4 mg versus subjects receiving placebo.
4                                              Teduglutide 4 mg/day for 10 days does not affect gastric
5                                              Teduglutide, a glucagon-like peptide 2 analogue, might r
6                                              Teduglutide, a recombinant analog of human glucagon-like
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 +/
11                                              Teduglutide had an intermediate effect on patients in gr
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
14                                              Teduglutide increased bromodeoxyuridine-positive cells v
15                                              Teduglutide increased Caco-2 proliferation but tended to
16              The MTS assay demonstrated that teduglutide increased cell numbers by a mean (SD) of 10%
17                                              Teduglutide increased plasma concentrations of citrullin
18                                              Teduglutide is a recombinant analogue of human glucagonl
19 the intestinal mucosa, and a GLP-2R agonist, teduglutide, is now used for augmentation of energy abso
20 tinuation was similar between patients given teduglutide (n = 2) and placebo (n = 3).
21                               The effects of teduglutide on absolute parenteral support volume were s
22 ve of this study was to assess the effect of teduglutide on gastric emptying of liquids in healthy su
23                      However, the effects of teduglutide on parenteral support vary among patients.
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
26 etaminophen absorption in subjects receiving teduglutide or placebo.
27                        Cells were exposed to teduglutide or vehicle control.
28                                              Teduglutide reduced the mean (SD) expression of villin b
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
34                         Twenty-four weeks of teduglutide treatment was generally well tolerated in pa

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