drugset / Trial / NCT06326476

Evaluate the Safety and Efficacy of Subcutaneous Siplizumab in the Treatment of Hidradenitis Suppurativa.

NCT06326476

Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study is to investigate the efficacy of siplizumab in the treatment of Hidradenitis Suppurativa.

Timeline

Start
2025-05-09
Primary completion
2027-12-31
Completion
2028-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Siplizumab Monoclonal antibody 10 mg Subcutaneous
Subject Siplizumab Monoclonal antibody 20 mg Subcutaneous
Subject Siplizumab Monoclonal antibody 40 mg Subcutaneous