Efficacy and Safety Evaluation of Osilodrostat in Cushing's Disease

Completed · Phase 3 · Has a placebo group

Conditions studied: Cushing's Disease

In brief

The purpose of this study was to confirm efficacy and safety of osilodrostat for the treatment of patients with Cushing's disease who are candidates for medical therapy.

Key facts

Study ID
NCT02697734
Run by
Novartis Pharmaceuticals
People needed
73
Starts
2016-10-03
Expected to finish
2020-12-31
Last updated by the study team
2021-11-01

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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