NCT03697109 · OUTCOME
Change in SBP and DBP During the OL Phase
A Study of the Efficacy and Safety of Relacorilant in Patients With Endogenous Cushing Syndrome · Source last updated 2025-07-16
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- mm Hg
- Interval / dispersion
- Standard Deviation
- Time frame
- Baseline and Week 22 (end of OL Phase)
What was measured
Blood pressure was measured by 24-hour ABPM.
Analysis population: The analysis population was patients in the mITT-OL Population who had HTN at Baseline.
Groups in this outcome
Relacorilant (OL Phase)
Patients will receive relacorilant increased sequentially from 100 mg once daily to a maximum dose of 400 mg once daily.
Relacorilant: Relacorilant is supplied as 100 mg capsules for oral dosing.
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| Relacorilant (OL Phase) | 102 |
|---|
Reported measurements
Baseline SBP
Analysis denominator · Participants
| Group | Source count |
|---|
| Relacorilant (OL Phase) | 101 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Relacorilant (OL Phase) | 140.66 | 10.66 | Not reported | Not reported | Not reported |
|---|
Change from Baseline in SBP at Week 22
Analysis denominator · Participants
| Group | Source count |
|---|
| Relacorilant (OL Phase) | 66 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Relacorilant (OL Phase) | -7.9 | 9.78 | Not reported | Not reported | Not reported |
|---|
Baseline DBP
Analysis denominator · Participants
| Group | Source count |
|---|
| Relacorilant (OL Phase) | 101 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Relacorilant (OL Phase) | 88.9 | 7.20 | Not reported | Not reported | Not reported |
|---|
Change from Baseline in DBP at Week 22
Analysis denominator · Participants
| Group | Source count |
|---|
| Relacorilant (OL Phase) | 66 |
|---|
Values in mm Hg · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Relacorilant (OL Phase) | -5.4 | 6.98 | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 10.66
- value
- 140.66
- title
- Baseline SBP
- categories
- measurements
- group Id
- OG000
- spread
- 9.78
- value
- -7.9
- title
- Change from Baseline in SBP at Week 22
- categories
- measurements
- group Id
- OG000
- spread
- 7.20
- value
- 88.9
- title
- Baseline DBP
- categories
- measurements
- group Id
- OG000
- spread
- 6.98
- value
- -5.4
- title
- Change from Baseline in DBP at Week 22
- description
- Blood pressure was measured by 24-hour ABPM.
- dispersion Type
- Standard Deviation
- groups
- description
- Patients will receive relacorilant increased sequentially from 100 mg once daily to a maximum dose of 400 mg once daily.
Relacorilant: Relacorilant is supplied as 100 mg capsules for oral dosing.
- id
- OG000
- title
- Relacorilant (OL Phase)
- param Type
- MEAN
- population Description
- The analysis population was patients in the mITT-OL Population who had HTN at Baseline.
- reporting Status
- POSTED
- time Frame
- Baseline and Week 22 (end of OL Phase)
- title
- Change in SBP and DBP During the OL Phase
- type
- OTHER_PRE_SPECIFIED
- unit Of Measure
- mm Hg
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice