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Nektar Therapeutics presented positive Phase IIb data for its atopic dermatitis (AD) candidate rezpeg (rezpegaldesleukin) at EADV 2025, driving significant stock gains. In the RESOLVE-AD trial (NCT06136741) involving 393 patients, mean Eczema Area and Severity Index (EASI) improvements were 61% for 24µg/kg every two weeks, 58% for 18µg/kg every two weeks, and 53% for 24µg/kg once monthly, versus 31% in placebo.
Key secondary endpoints, including EASI-75, EASI-90, vIGA-AD 0/1, Itch NRS, and Body Surface Area reductions, also favored the higher-dose cohorts. Extended dosing beyond 16 weeks further deepened clinical effects, with enhanced EASI reductions and higher response rates, according to Professor Jonathan Silverberg.
Rezpeg, an IL-2 pathway agonist and regulatory T-cell proliferator, was initially co-developed with Eli Lilly, but Nektar now independently leads development. The therapy offers a potential alternative to established treatments like Sanofi/Regeneron’s Dupixent, particularly for moderate-to-severe AD patients unresponsive to corticosteroids.
23-09-2025