drugset / Trial / NCT06900010

A Study to Evaluate CM336 in Adults With Autoimmune Bullous Disease

NCT06900010

Phase 2 Recruiting 30 enrolled Shandong First Medical University
NaSingle-groupOpen-labelTreatment

Summary

to Evaluate the Efficacy and Safety of CM336 (BCMA/CD3 Bispecific Antibody) in Adults with Moderate to Severe Autoimmune Bullous Disease

Timeline

Start
2025-04-22
Primary completion
2027-01-01
Completion
2028-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject CM336 Monoclonal antibody Subcutaneous