Coadministration of probenecid and cimetidine with mirogabalin in healthy subjects: A phase 1, randomized, open-label, drug-drug interaction study

Br J Clin Pharmacol. 2018 Oct;84(10):2317-2324. doi: 10.1111/bcp.13674. Epub 2018 Aug 9.

Abstract

Aims: The primary aim of this study was to assess the individual effects of probenecid and cimetidine on mirogabalin exposure.

Methods: This phase 1, open-label, crossover study randomized healthy adults to receive three treatment regimens, each separated by ≥5-day washout: a single oral dose of mirogabalin 15 mg on day 2, mirogabalin 15 mg on day 2 plus probenecid 500 mg every 6 h from days 1 to 4, and mirogabalin 15 mg on day 2 plus cimetidine 400 mg every 6 h from days 1 to 4.

Results: Coadministration of mirogabalin with probenecid or cimetidine increased the maximum and total mirogabalin exposure. The geometric mean ratios of Cmax and AUC(0-t) (90% CI) with and without coadministration of probenecid were 128.7% (121.9-135.7%) and 176.1% (171.9-180.3%), respectively. The geometric mean ratios of Cmax and AUC(0-t) (90% CI) with and without coadministration of cimetidine were 117.1% (111.0-123.6%) and 143.7% (140.3-147.2%), respectively. Mean (standard deviation) renal clearance of mirogabalin (l h-1 ) was substantially slower after probenecid [6.67 (1.53)] or cimetidine [7.17 (1.68)] coadministration, compared with mirogabalin alone [11.3 (2.39)]. Coadministration of probenecid or cimetidine decreased mirogabalin mean (standard deviation) apparent total body clearance [10.5 (2.33) and 12.8 (2.67) l h-1 , respectively, vs. 18.4 (3.93) for mirogabalin alone].

Conclusions: A greater magnitude of change in mirogabalin exposure was observed when coadministered with a drug that inhibits both renal and metabolic clearance (probenecid) vs. a drug that only affects renal clearance (cimetidine). However, as the increase in exposure is not clinically significant (>2-fold), no a priori dose adjustment is recommended.

Keywords: drug interactions; pain; pharmacokinetics.

Publication types

  • Clinical Trial, Phase I
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Area Under Curve
  • Bridged Bicyclo Compounds / administration & dosage
  • Bridged Bicyclo Compounds / pharmacokinetics*
  • Cimetidine / administration & dosage
  • Cimetidine / pharmacokinetics*
  • Cross-Over Studies
  • Diabetic Neuropathies / complications
  • Diabetic Neuropathies / drug therapy
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Drug Therapy, Combination / methods
  • Female
  • Healthy Volunteers
  • Herpes Zoster / complications
  • Herpes Zoster / drug therapy
  • Humans
  • Male
  • Metabolic Clearance Rate / drug effects*
  • Middle Aged
  • Neuralgia / drug therapy
  • Neuralgia / etiology
  • Probenecid / administration & dosage
  • Probenecid / pharmacokinetics*
  • Renal Elimination / drug effects

Substances

  • Bridged Bicyclo Compounds
  • Cimetidine
  • Probenecid
  • mirogabalin