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A Study to Evaluate the Efficacy and Safety of CBP-201 in Moderate to Severe Atopic Dermatitis in China

Moderate-to-severe Atopic Dermatitis Clinical Trial

Official title:
A Double-blind, Multi-center, Randomized Controlled Clinical Study to Evaluate the Efficacy and Safety of CBP-201 in Chinese Subjects With Moderate to Severe Atopic Dermatitis

Clinical Trial Summary

This study will evaluate the efficacy and safety of CBP-201 in Chinese subjects with moderate to severe atopic dermatitis.

Clinical Trial Description

This study is a randomized, double-blind, multi-center, controlled study designed to assess the efficacy, safety and PK characteristics of CBP-201 in eligible subjects with moderate to severe AD. The study includes a screening period, a treatment period and a follow-up period. The treatment period is divided into two stages. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05017480
Study type Interventional
Source Suzhou Connect Biopharmaceuticals, Ltd.
Contact
Status Completed
Phase Phase 2
Start date August 31, 2021
Completion date September 28, 2023
View Details
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