- Nektar Therapeutics presented Phase 2b data at 2026 American Academy of Dermatology meeting for rezpegaldesleukin in moderate-to-severe atopic dermatitis.
- REZOLVE-AD study enrolled 393 patients, showing statistically significant improvement in mean percent EASI improvement versus placebo across baseline vIGA-AD severity 3 or 4.
- Trial also reported comparable EASI-75 and EASI-90 response rates during 16-week induction period across moderate and severe subgroups.
- Separate late-breaking oral presentation highlighted Phase 2b REZOLVE-AA results in severe-to-very-severe alopecia areata at 36 weeks.
- High-dose rezpegaldesleukin 24 µg/kg every two weeks cut mean SALT score 28.2% versus 11.2% for placebo; Nektar plans to start Phase 3 ZENITH-AD program in second quarter 2026.
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. Nektar Therapeutics published the original content used to generate this news brief via PR Newswire (Ref. ID: 202603281236PR_NEWS_USPR_____SF20824) on March 28, 2026, and is solely responsible for the information contained therein.
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