Connect Biopharma (CNTB) Leerink Global Healthcare Conference 2026 summary
Event summary combining transcript, slides, and related documents.
Leerink Global Healthcare Conference 2026 summary
10 Mar, 2026Strategic pipeline and clinical development
Advancing a next-generation IL-4 receptor alpha monoclonal antibody (rademikibart) with rapid onset in atopic dermatitis and asthma, showing dramatic FEV1 improvements within 24 hours and potential for acute exacerbation treatment.
Phase II studies for acute asthma and COPD are underway, with topline results expected mid-year and IV formulation data anticipated late this quarter; Phase 3 studies are planned to follow.
Unique binding profile leads to greater receptor internalization, resulting in differentiated safety (modest eosinophil decline) and efficacy compared to existing therapies, with improved outcomes over dupilumab.
Product demonstrates longer functional half-life, maintaining efficacy at Q4 week dosing, with significant, sustained FEV1 gains as early as Day 1 and over 60% reduction in exacerbation rates compared to placebo.
Enrollment strategies include both ER-based and pre-enrollment through specialists, with global site activation to ensure timely data delivery.
Key scientific and clinical insights
Rademikibart rapidly reverses IL-13-induced hyporesponsiveness to β-agonists, resulting in faster and greater FEV1 improvement.
Rademikibart lowers eosinophil counts, reducing risk of serious adverse events, unlike dupilumab which increases eosinophils.
Q4W dosing in atopic dermatitis maintained efficacy, supporting less frequent dosing regimens.
Development pipeline and regulatory milestones
NDA approval for atopic dermatitis in China anticipated mid-2026, with global rights (outside Greater China) secured and partnership with Simcere including $110 million in milestones and tiered royalties.
FDA has agreed rademikibart can proceed to Phase 3 for chronic asthma and to parallel Phase 2 studies for acute exacerbations.
Manufacturing process improvements and tech transfer to US CMO completed, supporting future commercialization.
Patent and regulatory exclusivity extend into the 2040s, supporting long-term value.
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