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Nebokitug, an anti-CCL24 monoclonal antibody, in patients with primary sclerosing cholangitis: A phase 2 study

  • Christopher L. Bowlus*
  • , Douglas Thorburn
  • , Stephen T. Barclay
  • , Deepak Joshi
  • , Maria Carlota Londoño
  • , Parvez Mantry
  • , Rifaat Safadi
  • , Revita Aricha
  • , Chris Cirillo
  • , Matt Frankel
  • , John Lawler
  • , Ilan Vaknin
  • , Adi Mor
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Introduction: – Nebokitug (CM-101) is an anti-CCL24 monoclonal antibody with anti-inflammatory and anti-fibrotic properties. This phase 2 study evaluated the safety, tolerability, and biological activity of nebokitug in patients with primary sclerosing cholangitis (PSC).Methods: – SPRING was a randomized, double-blind, placebo-controlled phase 2 study in which patients with large duct PSC were randomized to receive either IV nebokitug 10 mg/kg, 20 mg/kg or placebo every 3 weeks for 15 weeks. The primary endpoint was safety and tolerability. Secondary endpoints included change from baseline to week 15 in liver blood tests, enhanced liver fibrosis (ELF) score, and liver stiffness measurements (LSM). Biological activity was explored in a prespecified subgroup with moderate/advanced fibrosis. Eligible patients who completed the 15-week double-blind period entered the open-label extension study to receive nebokitug for a total of 48 weeks.Results: – A total of 76 patients were enrolled and received at least 1 dose of nebokitug (n=56) or placebo (n=20). Frequency and severity of treatment-emergent adverse events were similar between the groups. No significant changes in liver tests, ELF scores and LSM from baseline to week 15 were observed in the total treatment population. However, in the prespecified subgroup of patients with moderate/advanced fibrosis (n=35), patients treated with nebokitug showed a significant reduction in LSM. Of the 54 patients eligible to participate, 50 enrolled in the OLE. Nebokitug continued to be well tolerated, and no new safety signal was observed.Conclusions: – Nebokitug was well-tolerated up to 48 weeks of treatment, and demonstrated numerical biomarker improvements in patients with PSC, particularly in those with moderate/advanced fibrosis.

Original languageEnglish
JournalAmerican Journal of Gastroenterology
VolumePublish Ahead of Print
DOIs
StatePublished - 1 Jan 2025
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2025

Keywords

  • CCL24
  • Enhanced Liver Fibrosis Score
  • Liver Stiffness Measurement
  • Nebokitug
  • Primary Sclerosing Cholangitis

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