drugset / Trial / NCT06301256

Evaluate the Efficacy of TIRZEPATIDE for the Treatment of Moderate to Severe HS Hidradenitis Suppurativa

NCT06301256

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the clinical efficacy and safety of tirzepatide in subjects with moderate to severe hidradenitis suppurativa. The study will be conducted over 24 weeks on active therapy followed by a eight-week observational follow-up visit. The total length of the study will be 32 weeks .

Timeline

Start
2024-03-11
Primary completion
2025-03-11
Completion
2025-03-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Tirzepatide Peptide