Connect Biopharma says rademikibart hits EASI-75 in 96.6% in Phase 3 AD trial

Reuters03-30

<a href="https://laohu8.com/S/CNTB">Connect Biopharma</a> says rademikibart hits EASI-75 in 96.6% in Phase 3 AD trial

Connect Biopharma disclosed Phase 3 52-week RADIANT-AD results for rademikibart in moderate-to-severe atopic dermatitis, already presented March 28 at 2026 American Academy of Dermatology annual meeting.
Trial enrolled 259 patients in China, testing rademikibart 300 mg every two weeks versus placebo for 16 weeks, followed by switch to active drug through Week 52.
Week 52 efficacy showed 96.6% achieved EASI-75, with 87.1% reaching IGA 0/1.
Safety profile was comparable to placebo at 16 weeks, with conjunctivitis rates not differentiated from placebo in induction phase.
Company highlighted optionality to pursue atopic dermatitis outside China based on durability through 52 weeks.

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 via GlobeNewswire (Ref. ID: 202603300701PRIMZONEFULLFEED9680469) on March 30, 2026, and is solely responsible for the information contained therein.

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