Connect Biopharma said rademikibart, an anti-IL-4Rα monoclonal antibody, has shown faster onset of action and greater FEV1 response in asthma trials. The company cited preclinical findings suggesting rademikibart differs from dupilumab in IL-4R binding and may improve responsiveness to β-agonist treatment in the presence of IL-13. Connect Biopharma said Phase 2 studies in acute asthma and COPD exacerbations began in 2Q2025, with topline data expected in mid-2026. It reported cash, cash equivalents and short-term investments of USD 54.8 million as of Sept. 30, 2025, expected to support planned operations into 2027. The presentation cited a dupilumab prescribing information link: https://www.regeneron.com/downloads/dupixent_fpi.pdf.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Connect Biopharma Holdings Ltd. published the original content used to generate this news brief on March 10, 2026, and is solely responsible for the information contained therein.
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