No intervention
OtherNo treatment (intervention) was administered.
NCT Number: NCT02663609
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.
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Notify Me18 year–85 year
All sexes
Observational
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
No treatment (intervention) was administered.
Time frame: up to 4 years
The retrospective review would analyze the drug utilization patterns of patients treated with Korlym
Time frame: up to 4 years
The retrospective review would analyze outcomes measures (vitals, clinical assessments, etc) in patients treated with Korlym
Corcept Therapeutics
Industry
Acronym: RE-KLAIM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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