Icanbelimod (CBP-307), a next-generation Sphingosine-1-phosphate receptor modulator, in healthy men: pharmacokinetics, pharmacodynamics, safety, and tolerability in a randomized trial in Australia

Front Immunol. 2024 Jun 17:15:1380975. doi: 10.3389/fimmu.2024.1380975. eCollection 2024.

Abstract

Background: Icanbelimod (formerly CBP-307) is a next-generation S1PR modulator, targeting S1PR1. In this first-in-human study, icanbelimod was investigated in healthy men in Australia.

Methods: Participants were randomized 3:1, double-blind, to icanbelimod or placebo in four single-dose cohorts (0.1 mg, 0.25 mg, 0.5 mg [n=8 per cohort], 2.5 mg [n=4]) or for 28-days once-daily treatment in two cohorts (0.15 mg, 0.25 mg [n=8 per cohort]). Participants in the 0.25-mg cohort received 0.1 mg on Day 1. Treatments were administered orally after fasting; following one-week washout, icanbelimod was administered after breakfast in the 0.5-mg cohort.

Results: Icanbelimod exposure increased rapidly and dose-dependently with single and multiple dosing (Tmax 4-7 hours). Lymphocyte counts decreased rapidly after single (-11%, 0.1 mg; -40%, 0.25 mg; -71%, 0.5 mg; -77%, 2.5 mg) and multiple doses (-49%, 0.15 mg; -75%, 0.25 mg), and recovered quickly, 7 days after dosing. After single-dose 0.5 mg, although a high-fat breakfast versus fasting did not affect maximal decrease, lymphocyte counts tended to be lower after breakfast across most timepoints up to 72 hours. Twenty-eight participants (63.6%) experienced mainly mild treatment-emergent adverse events (TEAEs). After single-dose icanbelimod, the most common TEAEs were headache (28.6%, n=6) and dizziness (19.0%, n=4). Three participants experienced transient bradycardia, with one serious, following single-dose 2.5 mg icanbelimod. After multiple-dose icanbelimod, the most common TEAEs were headache (50.0%, n=6) and lymphopenia (41.7%, n=5), and two participants withdrew due to non-serious TEAEs. Up-titration attenuated heart rate reductions.

Conclusion: Icanbelimod was well-tolerated up to 0.5 mg and effectively reduced lymphocyte counts.

Clinical trial registration: ClinicalTrials.gov, identifier NCT02280434.b.

Keywords: CBP-307; Sphingosine-1-phosphate receptor modulator; icanbelimod; lymphocyte reduction; pharmacodynamics; pharmacokinetics; safety.

Publication types

  • Randomized Controlled Trial
  • Clinical Trial, Phase I

MeSH terms

  • Adolescent
  • Adult
  • Australia
  • Double-Blind Method
  • Healthy Volunteers*
  • Humans
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Sphingosine 1 Phosphate Receptor Modulators* / administration & dosage
  • Sphingosine 1 Phosphate Receptor Modulators* / adverse effects
  • Sphingosine 1 Phosphate Receptor Modulators* / pharmacokinetics
  • Sphingosine-1-Phosphate Receptors
  • Young Adult

Substances

  • Sphingosine 1 Phosphate Receptor Modulators
  • Sphingosine-1-Phosphate Receptors

Associated data

  • ClinicalTrials.gov/NCT02280434

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article.