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AnaptysBio (ANAB) investor relations material
AnaptysBio Status Update summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Strategic and Company Structure Updates
Plans to separate into two independent public companies in 2026: one focused on biopharma R&D and commercialization, the other on royalty management.
The biopharma entity will advance therapeutics for autoimmune diseases, including ANB033 and rosnilimab.
The royalty management entity will manage rights to Jemperli (GSK) and Imsidolimab (Vanda), with minimal infrastructure.
Q2 2025 cash position is ~$294M, with expected runway through 2027, excluding significant royalty potential.
ANB033 Program Overview and Mechanism
ANB033 is a CD122 antagonist designed for high potency and dual inhibition of IL-15 and IL-2 signaling, targeting pathogenic immune cells in inflamed tissue.
Targets cytotoxic CD8+ T cells, memory CD4+ T cells, IELS, ILC2s, and NK cells, while sparing regulatory T cells.
Subcutaneous dosing achieves full receptor occupancy for over 30 days, with favorable pharmacokinetics and safety profile.
Demonstrated strong preclinical efficacy in models of GvHD and celiac disease, reducing cytolytic gene expression and preserving tissue integrity.
In EOE, ANB033 targets both CD4+ ILC2 and CD8+ NK cell pathways, potentially offering broader efficacy than current therapies.
Clinical Development and Trial Design
Phase 1a in healthy volunteers (n=60 ANB033, n=20 placebo) showed favorable safety, tolerability, and PK/PD profile, with no serious adverse events or discontinuations.
ANB033 significantly reduced CD122+ CD8+ T cells and NK cells after a single dose, with effects limited to CD122-expressing cells.
Phase 1b in celiac disease includes two cohorts: one for prevention of gluten-induced injury (Vh:Cd ≥2.0) and one for healing established mucosal damage (Vh:Cd <2.0), each enrolling 30 patients.
Primary endpoints include change in Vh:Cd ratio, IEL count, and patient-reported outcomes (CDSD), with results expected by year-end 2026.
Sites are located in Western EU, Australia, and New Zealand.
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