Treatment for Endogenous Cushing's Syndrome

Completed · Phase 3

Conditions studied: Endogenous Cushing's Syndrome

In brief

The primary objectives of this study are to evaluate the clinical responder rate, defined as the proportion of subjects with normal UFC after 6 months of treatment with COR-003 in the Maintenance Phase without dose increase, and to evaluate the range of effective doses in subjects with various levels of hypercortisolism.

Key facts

Study ID
NCT01838551
Run by
Cortendo AB
People needed
94
Starts
2014-08-01
Expected to finish
2018-11-01
Last updated by the study team
2021-04-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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