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Osilodrostat for the Treatment of Non-Cushing's Disease Cushing's Syndrome — LINC7  

Cushing's Syndrome Clinical Trial

Official title:
A Retrospective Observational Study to Evaluate the Safety and Effectiveness of Osilodrostat for the Treatment of Non-Cushing's Disease Cushing's Syndrome (LINC7)

Clinical Trial Summary

This is a multi-centre, observational, non-comparative, retrospective cohort study designed to evaluate the long-term safety and effectiveness of osilodrostat in non-CD CS patients. Patients treated with oral osilodrostat regardless of the duration of their treatment will be followed retrospectively for up to 36 months after initiating osilodrostat.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05633953
Study type Observational
Source RECORDATI GROUP
Contact
Status Completed
Phase
Start date January 16, 2023
Completion date October 30, 2023
View Details
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