BMS-981164
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February 10, 2026
Engineering and Development of a Novel Bispecific Antibody Targeting IL13 and IL31
(AAAAI 2026)
- "Results The bsAb demonstrates sub-nanomolar affinity for IL13, effectively inhibiting IL13-induced downstream signaling and TF-1 cell proliferation, with potency comparable to the benchmark Lebrikizumab analogue. Meanwhile, the bsAb shows sub-nanomolar affinity for IL31 and similar blocking activity to BMS-981164 in both IL31R reporter and CCL2 release assays. Furthermore, the bsAb exhibits a synergistic effect in IL13 and IL31-induced DU145 cell activation, surpassing the efficacy of each individual Conclusions The bsAb simultaneously blocks IL13 and IL31, effectively inhibiting key inflammatory signals and pruritus symptoms, while also exhibiting a synergistic effect. It holds great potential to improve therapeutic efficacy for patients with atopic dermatitis and other skin inflammation."
Atopic Dermatitis • Dermatitis • Dermatology • Immunology • Inflammation • Pruritus • CCL2 • IL13 • IL1R1 • IL6
February 20, 2024
A Bispecific, Tetravalent Antibody Targeting Inflammatory and Pruritogenic Pathways in Atopic Dermatitis.
(PubMed, JID Innov)
- "In reporter cell lines, NM26-2198 concomitantly inhibited IL-4/IL-13 and IL-31 signaling with a potency comparable with that of the combination of an anti-IL-4Rα antibody (dupilumab) and an anti-IL-31 antibody (BMS-981164). In a repeat-dose, good laboratory practice toxicology study in cynomolgus monkeys, no adverse effects of NM26-2198 were observed at a weekly dose of 125 mg/kg. Together, these results justify the clinical investigation of NM26-2198 as a treatment for moderate-to-severe AD."
Journal • Atopic Dermatitis • Dermatitis • Dermatology • Immunology • Inflammation • Pruritus • FCER2 • FCGR2A • FCGR2B • IL13 • IL4
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