drugset / Trial / NCT05987423

Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Participants With Thyroid Eye Disease

NCT05987423

Phase 3 Active not recruiting 131 enrolled Hoffmann-La Roche
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the efficacy, safety, pharmacokinetics, and pharmacodynamics of subcutaneous (SC) satralizumab, a recombinant, humanized anti-interleukin-6 (IL-6) receptor monoclonal antibody, in participants with thyroid eye disease (TED).

Timeline

Start
2023-10-26
Primary completion
2025-07-08
Completion
2026-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Satralizumab Monoclonal antibody Subcutaneous