Jefferies Global Healthcare Conference 2026
Logotype for Nektar Therapeutics

Nektar Therapeutics (NKTR) Jefferies Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Nektar Therapeutics

Jefferies Global Healthcare Conference 2026 summary

3 Jun, 2026

Pipeline and scientific focus

  • Emphasis on regulatory T cell biology, with rezpegaldesleukin as the lead asset showing efficacy in atopic dermatitis, alopecia areata, lupus, and psoriasis.

  • Advancing a TNFR2 agonist program targeting different Treg subsets, with plans for an IND filing next year.

  • Rezpegaldesleukin is positioned as an agonist, differentiating it from other pipeline drugs that are antagonists targeting IL-4, IL-13, IL-31, or TSLP.

  • Demonstrated broad activity across Th1, Th2, and Th17 mediated diseases, including comorbidities like asthma.

  • Durability of effect observed, with infrequent dosing maintaining response for extended periods.

Phase III clinical development for atopic dermatitis

  • Phase III program for atopic dermatitis has begun, with first sites opening this month and first patient randomization expected in July.

  • Three pivotal trials: two in biologic-naive adolescents and adults, and one in biologic-experienced patients, each enrolling 510 participants.

  • Induction phase lasts 24 weeks, followed by maintenance with monthly or quarterly dosing, and re-randomization to placebo or continued treatment.

  • Top-line induction data from the first bio-naive study expected mid-2028.

  • Global trial includes APAC sites, with confidence in efficacy across diverse genetic backgrounds.

Study design and regulatory strategy

  • Separate trials for biologic-naive and biologic-experienced populations to enable differentiated labeling and strategic positioning.

  • Large, highly powered studies designed to build a robust safety database for BLA submission.

  • Conservative statistical assumptions for biologic-experienced group, with missing data handled by multiple imputation.

  • Discontinuation rates expected to be lower in phase III due to improved trial design and patient expectations.

  • One-year safety data will anchor the initial BLA, with longer-term extension data to support future label updates.

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