drugset / Trial / NCT06884891

A Phase Ⅲ Comparative Study of QL2108 to Dupixent®

NCT06884891

Phase 3 Not yet recruiting 520 enrolled Qilu Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

It is a multicenter randomized, double-blinded, parallel, positive-controlled, Phase Ⅲ comparative study to evaluate the efficacy and safety of QL2108 to Dupixent® in adult subjects with moderate-to-severe atopic dermatitis. A total of 520 subjects are planned to be included and randomized at a ratio of 1:1 to receive QL2108 injection or Dupixent®

Timeline

Start
2025-04
Primary completion
2027-05
Completion
2028-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dupilumab Monoclonal antibody 300 mg Subcutaneous
Subject QL2108 Unknown 300 mg Subcutaneous

Indications