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Nektar, Continuing Comeback, Says Eczema Drug’s Effects Hold up in Follow-up Study

Nektar's 52-week REZOLVE-AD trial showed up to 83% sustained EASI-75 response and favorable safety, supporting rezpegaldesleukin's advancement to Phase 3 studies.

  • On Tuesday, February 10, 2026, Nektar Therapeutics announced positive 52-week REZOLVE-AD maintenance results and hosted a webcast to review topline data.
  • The global REZOLVE-AD Phase 2b study enrolled 393 patients with moderate-to-severe atopic dermatitis across approximately 110 sites globally, using a 16-week induction and randomized 3:3:3:2.
  • In the maintenance period, 24 μg/kg dosing maintained EASI-75 in 71% and 83% of responders and vIGA-AD 0/1 in 85% and 63%, with increased EASI-100 conversions and deeper responses at Week 52.
  • Nektar and investigators said safety was consistent with induction, 72% TEAEs for rezpegaldesleukin, mostly mild injection-site reactions, supporting advancement to Phase 3 studies.
  • With Fast Track designation, experts said rezpegaldesleukin, a first-in-class Treg biologic, shows potential for rapid development in atopic dermatitis.
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Nektar to Hold Conference Call to Discuss Topline Results from the 36-Week Maintenance Period for its REZOLVE-AD Phase 2b Study of Rezpegaldesleukin in Atopic Dermatitis on February 10, 2026

SAN FRANCISCO, Feb. 9, 2026 /PRNewswire/ -- Nektar Therapeutics (Nasdaq: NKTR), a clinical-stage biotechnology company focused on the development of novel immunology therapies, today announced it will host an investor call and live webcast to review topline results from the…

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KITV4 News broke the news in Honolulu, United States on Monday, February 9, 2026.
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