Chemomab Therapeutics (CCMB) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
20 Mar, 2026Nebokitug 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.
Latest events from Chemomab Therapeutics
- FDA-aligned Phase 3 path for nebokitug in PSC, improved financials, and strong clinical data.CCMB
Q4 202519 Mar 2026 - Nebokitug advances to phase III in PSC after strong phase II results, targeting major unmet needs.CCMB
Oppenheimer 36th Annual Healthcare Life Sciences Conference26 Feb 2026 - CM-101 showed strong safety and efficacy in Phase 2 PSC, supporting advancement to Phase 3.CCMB
Study Result3 Feb 2026 - CM-101 showed strong Phase II results in PSC and is advancing to a global Phase III trial.CCMB
Oppenheimer 35th Annual Healthcare Life Sciences Conference 202524 Dec 2025 - Registering 8.1M ADSs for resale after $10M financing to fund rare disease antibody development.CCMB
Registration Filing16 Dec 2025 - Regulatory and clinical milestones position nebokitug for a pivotal Phase 3 PSC trial.CCMB
Q3 202521 Nov 2025 - Nebokitug's phase II success in PSC paves the way for a pivotal phase III and potential first approval.CCMB
H.C. Wainwright 27th Annual Global Investment Conference20 Oct 2025 - Phase 3 prep for nebokitug in PSC advances, with strong data, new patents, and cash runway to 2026.CCMB
Q2 202512 Sep 2025 - Positive Phase 2 data for CM-101 in PSC supports Phase 3 plans and extends cash runway to 2026.CCMB
Q3 202413 Jun 2025