drugset / Trial / NCT05186922

The Study of CM326 in Patients With Moderate-to-severe Atopic Dermatitis

NCT05186922 ↗

Phase 1/2 Unknown 54 enrolled Keymed Biosciences Co.Ltd
RandomizedSequentialQuadruple-blindTreatment

Summary

This is a multi-center, randomized, double blind, placebo-controlled multiple dose escalation study to evaluate the safety, tolerance, PK, PD, immunogenicity and preliminary efficacy of CM326 in moderate-severe AD subjects.

Timeline

Start
2022-02-17
Primary completion
2023-01
Completion
2023-01

Drugs

EvaluationDrugModalityDoseRoute
Subject OCANKITUG Monoclonal antibody 55 mg Subcutaneous
Subject OCANKITUG Monoclonal antibody 110 mg Subcutaneous
Subject OCANKITUG Monoclonal antibody 220 mg Subcutaneous

Indications