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LY2963016 Insulin Glargine and Insulin Glargine (Lantus) Produce Comparable Pharmacokinetics and Pharmacodynamics at Two Dose Levels.
Zhang, Xin; Lam, Eric Chen Quin; Seger, Mary E; Coutant, David; Chua, Laiyi; Tan, Lai Hock; Soon, Danny; Linnebjerg, Helle.
Afiliación
  • Zhang X; Eli Lilly and Company, Indianapolis, IN, USA.
  • Lam ECQ; Formerly of Lilly-NUS Centre for Clinical Pharmacology, Singapore, Singapore.
  • Seger ME; Formerly of Eli Lilly and Company, Indianapolis, IN, USA.
  • Coutant D; Eli Lilly and Company, Indianapolis, IN, USA.
  • Chua L; Lilly-NUS Centre for Clinical Pharmacology, Singapore, Singapore.
  • Tan LH; Lilly-NUS Centre for Clinical Pharmacology, Singapore, Singapore.
  • Soon D; Formerly of Lilly-NUS Centre for Clinical Pharmacology, Singapore, Singapore.
  • Linnebjerg H; Eli Lilly and Company, Indianapolis, IN, USA.
Clin Pharmacol Drug Dev ; 6(6): 556-563, 2017 Nov.
Article en En | MEDLINE | ID: mdl-28940840
ABSTRACT
LY2963016 (LY IGlar) and Lantus (IGlar) are insulin glargine products with identical amino acid sequences. This was a phase 1 single-site, randomized, subject- and investigator-blinded, 4-treatment, 4-period crossover study to compare the pharmacokinetic (PK) and pharmacodynamic (PD) properties of LY IGlar and IGlar at 2 different doses. Fasted healthy subjects were randomly assigned to receive 2 single doses of LY IGlar and IGlar (0.3 and 0.6 U/kg for each product). Blood samples were collected up to 24 hours postdose to assess PK, and a euglycemic clamp lasting up to 24 hours postdose was conducted to assess PD. Twenty-four healthy subjects aged 23 to 52 years participated in the study. The primary PK parameters (area under the concentration versus time curve from 0 to 24 hours [AUC0-24 ] and maximum observed drug concentration [Cmax ]) and PD parameters (total amount of glucose infused during the clamp [Gtot ] and maximum glucose infusion rate [Rmax ]) were not statistically different between LY IGlar and IGlar at either dose. No safety concerns were noted with either drug. The study demonstrated that the PK and PD parameters for LY IGlar and IGlar were comparable following single doses at both 0.3 and 0.6 U/kg.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insulina Glargina / Hipoglucemiantes Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Pharmacol Drug Dev Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Insulina Glargina / Hipoglucemiantes Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Pharmacol Drug Dev Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos