drugset / Trial / NCT04838860

Siltuximab In Siltuximab-RElapsed/REfractory Multicentric CAstleman Disease

NCT04838860

Phase 2 Terminated 22 enrolled RECORDATI GROUP
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Phase 2 study to investigate the safety, tolerability, and efficacy of administering increased siltuximab doses to patients with iMCD

Timeline

Start
2021-03-31
Primary completion
2021-04-01
Completion
2021-04-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Siltuximab Monoclonal antibody 22 mg/kg Intravenous
Comparator Siltuximab Monoclonal antibody 33 mg/kg Intravenous
Comparator Siltuximab Monoclonal antibody 44 mg/kg Intravenous