The phase 2 Alluvium trial evaluated vamikibart's efficacy and safety in treatment-naïve patients with diabetic macular edema (DME).
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Vamikibart demonstrated average gains of approximately 6 letters in best-corrected visual acuity (BCVA) across all dosing arms at weeks 44 and 48.
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30% to 40% of treatment-naïve patients achieved resolution of DME, with central subfield thickness improvements of 50 µm to 70 µm from baseline.
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Higher doses of vamikibart were associated with increased intraocular inflammation, while low rates of cataract and elevated intraocular pressure were observed.
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The findings support further exploration of combining anti-IL-6 and anti-VEGF therapies to address both inflammatory and angiogenic pathways in DME.