Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Lisbeth V. Jacobsen"'
Publikováno v:
Clinical Pharmacokinetics
Background and Objectives This analysis used a population pharmacokinetic approach to identify covariates that influence plasma exposure of liraglutide 3.0 mg, a glucagon-like peptide-1 (GLP-1) receptor agonist approved for weight management in overw
Autor:
Rune Viig Overgaard, Lisbeth V. Jacobsen, Christine B. Jensen, John P.H. Wilding, C. W. le Roux
Publikováno v:
Diabetes, Obesity & Metabolism
Aims Liraglutide 3.0 mg, an acylated GLP-1 analogue approved for weight management, lowers body weight through decreased energy intake. We conducted exposure-response analyses to provide important information on individual responses to given drug dos
Publikováno v:
Clinical Pharmacokinetics
Liraglutide is an acylated glucagon-like peptide-1 analogue with 97 % amino acid homology with native glucagon-like peptide-1 and greatly protracted action. It is widely used for the treatment of type 2 diabetes mellitus, and administered by subcutan
Autor:
Paula M Hale, Silva A. Arslanian, Tadej Battelino, Lisbeth V. Jacobsen, D J Chatterjee, David J. Klein
Publikováno v:
Diabetes Technology & Therapeutics. 16:679-687
The prevalence of type 2 diabetes (T2D) in youth is increasing. Treatment options beyond metformin and insulin are needed. The safety, tolerability, pharmacokinetics, and pharmacodynamics of liraglutide once daily in youth (10-17 years old) with T2D
Autor:
K Kapitzke, Thomas Danne, Torben Biester, Lisbeth V. Jacobsen, Kristin C. Carlsson Petri, Olga Kordonouri, Paula M Hale, Sanja Hald Jacobsen
Publikováno v:
The Journal of pediatrics. 181
Objectives To investigate the safety, tolerability, and pharmacokinetics of liraglutide in adolescents with obesity. Study design This was a randomized, double-blind, placebo-controlled trial. Twenty-one subjects, aged 12-17 years and Tanner stage 2-
Publikováno v:
The Journal of Clinical Pharmacology. 51:1696-1703
Liraglutide is a once-daily human GLP-1 analog for treatment of type 2 diabetes. Like other GLP-1 analogs, liraglutide delays gastric emptying, which could potentially affect absorption of concomitantly administered oral drugs. This study investigate
Publikováno v:
The Journal of Clinical Pharmacology. 50:886-894
The once-daily human glucagon-like peptide-1 (GLP-1) analog, liraglutide, was recently shown to provide improved glycemic control in subjects with type 2 diabetes (T2D) compared with exenatide. The aim of this work is to estimate the population pharm
Publikováno v:
Journal of clinical pharmacology. 55(12)
Insulin degludec/liraglutide (IDegLira) is a novel fixed-ratio combination of the basal insulin insulin degludec (IDeg) and liraglutide, a glucagon-like peptide-1 analog. The pharmacokinetics (PK) and pharmacodynamics of IDegLira were assessed versus
Publikováno v:
Clinical Pharmacokinetics
Background and Objective The safety, tolerability, and pharmacokinetics of the once-daily human glucagon-like peptide-1 (GLP-1) analog liraglutide have been evaluated in pediatric patients aged greater than 10 years with type 2 diabetes (T2D). In thi
Publikováno v:
Clinical Therapeutics. 24:530-539
Objective: The purpose of this study was to compare the pharmacokinetics and pharmacodynamics of the premixed insulin analogue biphasic insulin aspart (BIAsp 30) with the equivalent premixed biphasic human insulin (BHI 30), administered twice daily,