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CompletedNCT02663609RE-KLAIMUpdated Jun 1, 2023

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

An observational study in Cushing's Syndrome, sponsored by Corcept Therapeutics. Completed. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2023-06-01.

Sponsored by Corcept Therapeutics · Observational

Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
24
Ages
18 Years to 85 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Cushing's Syndrome

Keywords

  • Cushing's Syndrome
  • Mifepristone
  • Adrenal
  • Retrospective
  • Chart Review
03

In context

Cushing Syndrome

123 studies on the registry are indexed under Cushing Syndrome; 37 are open to participants now.

This study's enrollment of 24 is below the median of 115 across 62 observational studies indexed under Cushing Syndrome.

Browse Cushing Syndrome studies →

Lead sponsor

Corcept Therapeutics is the lead sponsor of 73 studies on the registry; 4 are open to participants now.

Of its 31 completed or terminated interventional studies of FDA-regulated products, 9 (29%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

ACTH Independent Cushing's Syndrome patients treated with Korlym® mifepristone) as standard of care in clinical practice.

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

Exclusion Criteria:

  • Diagnosed with adrenocortical carcinoma
  • Participant in any clinical trial(s) during the observational period
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
24 participants (actual)
Patient registry
No

Interventions

  • OtherNo intervention

    No treatment (intervention) was administered.

06

What researchers measure

Primary outcomes

  1. Drug Utilization Patterns as assessed by chart review

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

    Time frame: up to 4 years

Secondary outcomes

  1. Clinical Outcomes as assessed by chart review

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

    Time frame: up to 4 years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 1, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02663609
Lead sponsor
Corcept Therapeutics
Responsible party
Sponsor
First posted
Jan 26, 2016
Start date
Oct 2015
Primary completion
Dec 1, 2017
Completion
Dec 1, 2017
Last update
Jun 1, 2023

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2023. You cannot join it, but the record below documents what was studied.

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