Randomized, open-label, comparative phase IV study on the bioavailability of Ciclosporin Pro (Teva) versus Sandimmun® Optoral (Novartis) under fasting versus fed conditions in patients with stable renal transplants

BMC Nephrol. 2019 May 14;20(1):167. doi: 10.1186/s12882-019-1340-z.

Abstract

Background: The influence of pre- or postprandial administration on pharmacokinetics of cyclosporine is supposed to be less in gel-based formulations than in microemulsions. This study was designed to investigate the influence of a high-fat meal on the pharmacokinetic profile of the two cyclosporine containing formulations Ciclosporin Pro (gel-based emulsion) and Sandimmun®Optoral (microemulsion) in renal transplant recipients.

Methods: A randomized, open-label, repeated-measurement, comparative phase IV trial was conducted with two sequence groups for nutrition condition (fasting→fed, fed→fasting) and two treatment phases (Sandimmun® Optoral → Ciclosporin Pro), each covering both nutrition conditions. Primary pharmacokinetic variable of interest was the reduction of bioavailability due to high-fat food compared to fasting conditions measured by the difference D of ln-transformed bioavailability variables (AUCSS, τ, Css, max, und Css, min).

Results: A nutrition effect was found for both study medications with respect to the parameters AUCSS, τ and CSS, max, but not to CSS, min. The reduction of bioavailability caused by high-fat food was not significantly different for Sandimmun®Optoral and Ciclosporin Pro.

Conclusions: An effect of high-fat breakfast prior to the morning dose on AUCSS, τ and CSS, max was found for Sandimmun® Optoral and for Ciclosporin Pro. Trough level monitoring did not capture ingestion-related variability. Conversion to Ciclosporin Pro seems to be safe with regard to intra-individual pharmacokinetic variability.

Trial registration: EudraCT No. 2009-011354-18 (29th April 2019).

Keywords: Bioavailability; Cyclosporine; Food intake; Gel-based emulsion; Microemulsion.

Publication types

  • Clinical Trial, Phase IV
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biological Availability
  • Cyclosporine / metabolism*
  • Diet, High-Fat* / trends
  • Drug Compounding / methods*
  • Drug Industry / trends
  • Fasting / metabolism*
  • Female
  • Humans
  • Immunosuppressive Agents / metabolism*
  • Kidney Transplantation* / trends
  • Male
  • Middle Aged
  • Single-Blind Method

Substances

  • Immunosuppressive Agents
  • Cyclosporine

Associated data

  • EudraCT/EudraCT 2009-011354-18