Corporate presentation
Logotype for Chemomab Therapeutics Ltd

Chemomab Therapeutics (CCMB) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Chemomab Therapeutics Ltd

Corporate presentation summary

20 Mar, 2026

Nebokitug clinical development and positioning

  • Nebokitug is a first-in-class, Phase 3-ready monoclonal antibody targeting CCL24, with first-to-market potential for primary sclerosing cholangitis (PSC), a rare liver disease with high unmet need and >$1B commercial opportunity.

  • Positive Phase 2 data in PSC demonstrated safety, anti-fibrotic, anti-inflammatory, and anti-cholestatic activity, derisking the Phase 3 program.

  • FDA End-of-Phase 2 meeting provided a clear, efficient pathway to full approval, with a single event-driven pivotal trial using a composite clinical endpoint.

  • Nebokitug also has a Phase 2-ready program for systemic sclerosis (SSC), another orphan disease with >$1.5B potential.

  • Orphan Drug and Fast Track designations in both PSC and SSC support regulatory and commercial advantages.

Mechanism of action and scientific rationale

  • Nebokitug neutralizes CCL24, a chemokine central to inflammation and fibrosis, directly activating fibroblasts and immune cell recruitment.

  • Preclinical and patient sample data show elevated CCL24 in PSC and SSC, correlating with disease severity and progression.

  • Animal models and ex vivo studies confirm anti-fibrotic and anti-inflammatory effects across multiple organs.

  • Nebokitug’s direct CCL24 inhibition offers advantages over receptor blockade, including favorable tolerability and reduced off-target effects.

Phase 2 SPRING trial results in PSC

  • Randomized, double-blind, placebo-controlled trial in 76 PSC patients showed good safety and tolerability at both 10 mg/kg and 20 mg/kg doses.

  • Statistically significant improvements in liver stiffness, ELF score, fibrotic biomarkers, pruritus, and bilirubin, especially in moderate/advanced disease at 20 mg/kg.

  • 48-week open-label extension confirmed durability of anti-fibrotic effects, reduced progression of liver stiffness, and fewer clinical events versus historical controls.

  • Safety profile remained favorable over 48 weeks, with most adverse events mild and similar across arms.

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