Effect of single and multiple doses of elobixibat, an ileal bile acid transporter inhibitor, on chronic constipation: A randomized controlled trial

Br J Clin Pharmacol. 2018 Oct;84(10):2393-2404. doi: 10.1111/bcp.13698. Epub 2018 Aug 2.

Abstract

Aims: Elobixibat is a minimally absorbed ileal bile acid transporter inhibitor. This study aimed to investigate the safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of elobixibat in Japanese patients with chronic constipation.

Methods: This study consisted of single-dose and multiple-dose tests with a dose-escalating design. Sixty patients including females and males were randomized into five dose levels of elobixibat (2.5, 5, 10, 15 or 20 mg, n = 10 per level) and corresponding placebo (n = 2 per group). A crossover design was used to examine food effect in single-dose test. Patients received test tablets once daily for 14 days in multiple-dose test. We assessed pharmacokinetic-dose proportionality, levels of serum high- and low-density lipoprotein cholesterol and plasma 7α-hydroxy-4-cholesten-3-one (C4), food effect and sex-specific effect. Adverse events and bowel functions such as bowel movements, stool consistency and straining were also evaluated.

Results: Food consumption reduced systemic exposure by around 80% [e.g. least squares mean (ratio of breakfast/no breakfast) maximum plasma concentration: 0.2085 (90% confidence interval, 0.1371-0.3172) at 15 mg] while increased plasma C4 level (P < 0.001). In the multiple-dose test, elobixibat reduced low-density lipoprotein cholesterol and increased C4 whilst unaltering high-density lipoprotein cholesterol level. The increased spontaneous bowel movement frequency was correlated with higher dosage and higher C4 level (R2 = 0.5929 at Week 2). Adverse events were mainly gastrointestinal symptoms, most of which were mild.

Conclusions: Elobixibat should be taken before breakfast. Once-daily administration of elobixibat was found to be safe and tolerated up to 20 mg in female and male patients with chronic constipation.

Keywords: gastroenterology; pharmacodynamics; pharmacokinetics; phase I; randomized controlled trial.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Carrier Proteins / antagonists & inhibitors*
  • Carrier Proteins / metabolism
  • Cholestenones / blood
  • Cholesterol, LDL / blood
  • Chronic Disease / drug therapy
  • Constipation / blood
  • Constipation / drug therapy*
  • Constipation / pathology
  • Cross-Over Studies
  • Defecation / drug effects
  • Dipeptides / pharmacology*
  • Dipeptides / therapeutic use
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Drug Administration Schedule
  • Female
  • Food-Drug Interactions
  • Humans
  • Ileum / drug effects
  • Ileum / metabolism
  • Ileum / pathology
  • Male
  • Membrane Glycoproteins / antagonists & inhibitors*
  • Membrane Glycoproteins / metabolism
  • Middle Aged
  • Placebos / administration & dosage
  • Placebos / adverse effects
  • Sex Factors
  • Tablets
  • Thiazepines / pharmacology*
  • Thiazepines / therapeutic use
  • Treatment Outcome
  • Young Adult

Substances

  • Carrier Proteins
  • Cholestenones
  • Cholesterol, LDL
  • Dipeptides
  • Membrane Glycoproteins
  • Placebos
  • Tablets
  • Thiazepines
  • bile acid binding proteins
  • 7 alpha-hydroxy-4-cholesten-3-one
  • elobixibat