H.C. Wainwright 27th Annual Global Investment Conference
Logotype for Chemomab Therapeutics Ltd

Chemomab Therapeutics (CCMB) H.C. Wainwright 27th Annual Global Investment Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Chemomab Therapeutics Ltd

H.C. Wainwright 27th Annual Global Investment Conference summary

20 Oct, 2025

Key presentations and announcements

  • Presented positive phase II results for nebokitug, a first-in-class monoclonal antibody targeting CCL24, in primary sclerosing cholangitis (PSC).

  • Nebokitug demonstrated significant anti-inflammatory and anti-fibrotic effects, meeting both primary (safety) and secondary (efficacy) endpoints in the phase II study.

  • The 20 mg/kg dose was selected for phase III, focusing on patients with moderate to advanced PSC.

  • High patient compliance observed, with 93% of eligible patients entering the open-label extension for up to 48 weeks.

  • FDA alignment achieved for a single pivotal phase III study, with plans to initiate soon and pursue full approval.

Industry analysis and competitive landscape

  • PSC is a rare liver disease with no approved treatments; current therapies only address symptoms, not disease progression.

  • Nebokitug is positioned as the only disease-modifying therapy in development for PSC, with potential to become the first approved drug for this indication.

  • Estimated commercial opportunity exceeds $1 billion annually due to high unmet need and premium pricing potential.

  • Strong interest from top-tier investors and potential strategic partners based on phase II results.

Forward-looking statements and development plans

  • Phase III study will evaluate clinical events beyond liver transplant and death, enabling a more feasible and timely trial.

  • Ongoing discussions with partners to support phase III initiation and commercialization.

  • Nebokitug's dual mechanism may have applications in other fibrotic diseases, with supporting data in systemic sclerosis and IPF.

  • Long-term safety and efficacy data support continued development and regulatory advancement.

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