drugset / Trial / NCT06092762

A Study to Evaluate the Safety and Efficacy of AK120 in Subjects With Moderate to Severe Atopic Dermatitis

NCT06092762 ↗

Phase 2 Completed 180 enrolled Akeso
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, randomized, open label phase II clinical study to evaluate the safety and efficacy of AK120 in the treatment of subjects with moderate to severe atopic dermatitis.

Timeline

Start
2023-11-06
Primary completion
2024-11-13
Completion
2024-11-13

Drugs

EvaluationDrugModalityDoseRoute
Subject AK120 Monoclonal antibody 300 mg Subcutaneous
Subject AK120 Monoclonal antibody 450 mg Subcutaneous

Indications