drugset / Trial / NCT04893941

Dose Escalation Trial of CM310 in Patients With Moderate-to-Severe Atopic Dermatitis (AD)

NCT04893941

Phase 1/2 Completed 39 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 subcutaneously CM310 in moderate-severe AD subjects.

Timeline

Start
2020-07-21
Primary completion
2021-01-22
Completion
2021-01-22

Drugs

EvaluationDrugModalityDoseRoute
Subject CM310 Monoclonal antibody 75 mg Subcutaneous
Subject CM310 Monoclonal antibody 150 mg Subcutaneous
Subject CM310 Monoclonal antibody 300 mg Subcutaneous

Indications