drugset / Trial / NCT06131580

Canadian Continuation of Roll-over Study in Patients With Endogenous Cushing's Syndrome

NCT06131580

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to continue the evaluation of long-term safety of osilodrostat in 7 Canadian patients who have already received osilodrostat treatment in a previous Global Recordati-sponsored roll-over study and who, based on investigators' judgement, will continue benefiting with its administration.

Timeline

Start
2023-10-24
Primary completion
2025-11-24
Completion
2025-11-24

Drugs

EvaluationDrugModalityDoseRoute
Subject osilodrostat Small molecule 1 mg Oral
Subject osilodrostat Small molecule 5 mg Oral
Subject osilodrostat Small molecule 10 mg Oral