Trial · NCT01371565
Compassionate Use of CORLUX® (Mifepristone) in the Treatment of Signs and Symptoms of Endogenous Cushing's Syndrome
NCT01371565, Phase 3, Completed, Corcept Therapeutics; results first posted 2013-11-20
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Compassionate Use of CORLUX® (Mifepristone) in the Treatment of Signs and Symptoms of Endogenous Cushing's Syndrome. Trials, record NCT01371565. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01371565
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Compassionate Use of CORLUX® (Mifepristone) in the Treatment of Signs and Symptoms of Endogenous Cushing's Syndrome
- NCT number
- NCT01371565
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 4 participants, actual
- Lead sponsor
- Corcept Therapeutics
- Conditions
- Cushing's Disease, Cushing's Syndrome
- Interventions
- Mifepristone
- First posted
- 2011-06-13
- Last updated
- 2014-03-18
- Results first posted
- 2013-11-20
Source ClinicalTrials.gov
Registered outcomes1
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants With Adverse Events | 6 months | Safety was assessed at all visits and adverse events were recorded. |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Adverse Events | 6 months | Due to the small number of patients enrolled (N=4), no formal assessments were planned. All patients who received study drug were included in the safety review. | participants | NUMBER |
Source ClinicalTrials.gov
Results by group1
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With Adverse Events | Mifepristone | 4 | participants |
Source ClinicalTrials.gov
Participant flow3
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Mifepristone | 4 | |
| Overall Study | COMPLETED | Mifepristone | 1 | |
| Overall Study | NOT COMPLETED | Mifepristone | 3 |
Source ClinicalTrials.gov
Adverse events48
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Pancytopenia | Blood and lymphatic system disorders | Mifepristone | 1 | 4 | 1 |
| other | Eye irritation | Eye disorders | Mifepristone | 1 | 4 | 1 |
| other | Dysphagia | Gastrointestinal disorders | Mifepristone | 1 | 4 | 1 |
| other | Dyspepsia | Gastrointestinal disorders | Mifepristone | 1 | 4 | 1 |
| other | Vomiting | Gastrointestinal disorders | Mifepristone | 1 | 4 | 1 |
| other | Influenza like illness | General disorders | Mifepristone | 1 | 4 | 1 |
| other | Swelling | General disorders | Mifepristone | 1 | 4 | 1 |
| other | Thirst | General disorders | Mifepristone | 1 | 4 | 1 |
| other | Asthenia | General disorders | Mifepristone | 1 | 4 | 1 |
| other | Fatigue | General disorders | Mifepristone | 1 | 4 | 1 |
1 to 10 of 48Source ClinicalTrials.gov
See all 48 adverse eventsAdverse event totals3
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Mifepristone | ||
| Total, other adverse events | Mifepristone | 4 | 4 |
| Total, serious adverse events | Mifepristone | 1 | 4 |
Source ClinicalTrials.gov
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01371565
GET https://conductscience.org/api/trials/v1/NCT01371565/events?page=2