Effect of steady-state atorvastatin on the pharmacokinetics of a single dose of colchicine in healthy adults under fasted conditions

Clin Drug Investig. 2014 Apr;34(4):259-67. doi: 10.1007/s40261-013-0168-8.

Abstract

Background and objective: Colchicine is commonly prescribed for gout. While minimally metabolized by the cytochrome P450 (CYP) 3A4 isoenzyme, colchicine is a substrate for P-glycoprotein (P-gp). Atorvastatin is metabolized primarily by CYP3A4 and is a P-gp inhibitor. Patients with gout often have dyslipidemia; therefore, the potential for co-administration of atorvastatin and colchicine exists. The objective of this study was to determine the effect of oral atorvastatin on the pharmacokinetics of a single, oral dose of colchicine.

Methods: Twenty-four healthy adult subjects were enrolled in this single-center, open-label, non-randomized, one-sequence, two-period drug-drug interaction study. On day 1, subjects received a single oral dose of colchicine 0.6 mg. After a 14-day washout, subjects received atorvastatin 40 mg once daily for 14 days followed by a single dose of colchicine 0.6 mg co-administered with atorvastatin 40 mg on day 28. Main outcome measures were colchicine maximum plasma concentration (C max), area under the plasma concentration-time curve (AUC) from time zero to the last measurable concentration (AUC last), and AUC from time zero to infinity (AUC∞), which were compared with and without concurrent atorvastatin.

Results: Colchicine AUC last, AUC∞, and C max increased by 27, 24, and 31 %, respectively, when co-administered with atorvastatin. Corresponding 90 % confidence intervals around the ratios were outside the established no-effect 80-125 % interval.

Conclusion: Increased colchicine exposure was observed after a single dose of colchicine was administered with steady-state atorvastatin. Additional studies with multiple dosing of both drugs are needed to further determine the clinical implications of these results.

Trial registration: ClinicalTrials.gov NCT00960323.

Publication types

  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anticholesteremic Agents / pharmacology*
  • Area Under Curve
  • Atorvastatin
  • Colchicine / administration & dosage*
  • Colchicine / pharmacokinetics*
  • Drug Interactions
  • Fasting*
  • Female
  • Gout Suppressants / administration & dosage*
  • Gout Suppressants / pharmacokinetics*
  • Healthy Volunteers
  • Heptanoic Acids / adverse effects
  • Heptanoic Acids / pharmacology*
  • Humans
  • Male
  • Pyrroles / adverse effects
  • Pyrroles / pharmacology*
  • Young Adult

Substances

  • Anticholesteremic Agents
  • Gout Suppressants
  • Heptanoic Acids
  • Pyrroles
  • Atorvastatin
  • Colchicine

Associated data

  • ClinicalTrials.gov/NCT00960323