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Retrospective Chart Review Study of Korlym for the Treatment of ACTH Independent Cushing's Syndrome

Completed
Conditions
Cushing's Syndrome
Registration Number
NCT02663609
Lead Sponsor
Corcept Therapeutics
Brief Summary

Chart review study to collect patient data from medical charts of patients who have been treated with Korlym® for the treatment of ACTH independent adrenal Cushing's Syndrome.

Detailed Description

A retrospective, multi-center, chart review study to collect patient data from medical charts of patients who have been treated with Korlym® for the treatment of ACTH independent adrenal Cushing's Syndrome. Treatment with Korlym® will be a minimum 3 months in duration with follow-up of a minimum 3 months. Only sites that have been identified to have patients appropriate for this protocol will be invited to participate.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Diagnosed with ACTH independent endogenous Cushing's Syndrome
  • Available adrenal imaging prior to being treated with Korlym®
  • Treated with Korlym® and followed for at least 3 months (follow-up data should be available)
Exclusion Criteria
  • Diagnosed with adrenocortical carcinoma
  • Participant in any clinical trial(s) during the observational period

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Drug Utilization Patterns as assessed by chart reviewup to 4 years

The retrospective review would analyze the drug utilization patterns of patients treated with Korlym

Secondary Outcome Measures
NameTimeMethod
Clinical Outcomes as assessed by chart reviewup to 4 years

The retrospective review would analyze outcomes measures (vitals, clinical assessments, etc) in patients treated with Korlym

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