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A roll-over Study in Patients With Endogenous Cushing's Syndrome

Phase 3
Completed
Registration Number
JPRN-jRCT2080222646
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
All
Target Recruitment
137
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
safety<br>efficacy<br>-
Secondary Outcome Measures
NameTimeMethod
efficacy
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