drugset / Trial / NCT05905133

A Study to Evaluate the Safety and Efficacy of CBP-201 in Chinese Adult Subjects With Moderate to Severe AD

NCT05905133 ↗

Phase 2 Unknown 360 enrolled Connect Biopharm LLC
NaSingle-groupOpen-labelTreatment

Summary

This study is a single-arm, open-label, multi-center clinical study designed to assess the safety and efficacy of CBP-201 in eligible subjects with moderate to severe Atopic Dermatitis.

Timeline

Start
2023-07-15
Primary completion
2024-06-30
Completion
2024-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject CBP-201 Unknown 300 mg Subcutaneous

Indications