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1.
Clin Pharmacol Drug Dev ; 12(4): 385-391, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36648126

RESUMO

Liraglutide, a glucagon-like peptide 1 receptor agonist, is indicated as an adjunct to diet and exercise to improve glycemic control in patients with type 2 diabetes. The original liraglutide products are costly, which limits patient access to this therapeutic treatment. Herein, a biosimilar was developed that is highly similar to the reference drug in molecular structure and bioactivity, and is expected to have similar pharmacokinetic (PK) and safety profiles in clinical studies. This study aimed to primarily evaluate the bioequivalence of 2 liraglutide formulations and secondarily assess their safety in healthy Chinese subjects following a single-dose subcutaneous injection. Thirty-two healthy volunteers were recruited in this randomized, open-label, single-dose, 2-period crossover bioequivalence study (ChiCTR2100043348). The geometric mean ratios (GMRs) of the test drug to the reference drug (T/R) and corresponding 90% confidence intervals (CIs) for maximum concentration (Cmax ) and the area under the concentration-time curve from time 0 to the time of the last quantifiable concentration (AUC0-t ) were estimated using a mixed-effects model, and bioequivalence was determined to have been achieved if the 2-sided 90%CI fell within the predefined range of 80%-125%. PK parameters were comparable between T and R, with GMRs of T/R for Cmax and AUC0-t being 105.7% and 107.7%, respectively, the 90%CI of which met the acceptance criteria for bioequivalence. We also observed a similar and favorable safety profile in the T and R arms, with adverse events being predominantly mild in severity and of gastrointestinal origin. Our findings indicate that the test drug is safe and well tolerated, bioequivalent to the reference drug, and warrants further testing in a phase III clinical trial.


Assuntos
Diabetes Mellitus Tipo 2 , Liraglutida , Humanos , Diabetes Mellitus Tipo 2/tratamento farmacológico , População do Leste Asiático , Voluntários Saudáveis , Liraglutida/uso terapêutico , Equivalência Terapêutica
2.
J Nanosci Nanotechnol ; 10(11): 7226-30, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-21137903

RESUMO

Amorphous Fe(73.5)Si(13.5)B9Nb3Cu1 alloy was prepared by the chill block melt-spinning process and nanocrystalline Fe(73.5)Si(13.5)B9Nb3Cu1 alloy was obtained by annealing. The crystallization behaviors were analysed by DSC, XRD and TEM. The electrochemical corrosion behaviors in different annealed states were performed by linear polarization method and electrochemical impedance spectroscopy in 3.5% NaCl solution. The results show that the crystallization of amorphous alloy occurs in the two steps. Some nanometer crystals appear when annealing in 550 degrees C and 600 degrees C, respectively with grain size 13 nm and 15 nm. The nanocrystalline alloy has a tendency to passivation and lower anodic current density than amorphous alloy. It indicates that nanocrystalline alloy has a higher corrosion resistance. Amorphous Fe(73.5)Si(13.5)B9Nb3Cu1 alloy consisted of only single semi-circle. When the alloy was annealed in 600 degrees C, its EIS consisted of two time constants, i.e., high frequency and low frequency capacitive loops. The charge transfer reaction resistances increases as annealing temperature rises.

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