HomeTrialNCT06340360
🔬NCT06340360Phase 2ACTIVE NOT RECRUITING

A Phase 2b Study to Evaluate Rezpegaldesleukin (Rezpeg) in the Treatment of Severe to Very Severe Alopecia Areata in Adult Patients (Rezolve AA)

Study Summary

This is an interventional, randomized, double blind, parallel group, placebo-controlled, Phase 2b, 3-arm study to assess the effect of pegylated-recombinant-human interleukin-2 (rezpegaldesleukin) in adult participants with severe to very severe alopecia areata. The estimated duration includes a screening period of up to 35 days, a 36-week treatment period, an optional 16-week treatment extension period, and a 24-week follow-up period. The maximum study duration is approximately 81 weeks for all participants.

Conditions
Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment94 participants
Primary Completion
Lead SponsorNektar Therapeutics
Data Retrieved2026-04-11 04:22:39.533939+00:00
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