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NCT06094725 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Effects of Hepatic Impairment on the Pharmacokinetics of Relacorilant
A Phase 1 study of Hepatic Impairment, sponsored by Corcept Therapeutics.
- Completed
- Registry status
- Phase 1
- Development phase
- 30
- Enrollment target
- 2
- Study locations
NCT06094725: Completed Phase 1 study of Hepatic Impairment, sponsored by Corcept Therapeutics.
NCT06094725 is a Phase 1 study of Hepatic Impairment that has completed, run by Corcept Therapeutics. The registered enrollment target is 30 participants, below the 36-participant average among 48 other Hepatic Impairment trials with a reported enrollment target (17% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06094725, a Phase 1 study of Hepatic Impairment, has completed, sponsored by Corcept Therapeutics.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 30 participants
- Enrollment target
- 2
- Study locations
Study Summary
The primary objective of this multiple-dose, adaptive design study is to evaluate the effect of hepatic impairment on the pharmacokinetics (PK) of relacorilant relative to healthy matched control male and female subjects (Part 1).
Conditions Studied
Interventions
- DRUG Relacorilant
Study Locations (2)
Florida
- Clinical Pharmacology of Miami, LLC - Miami
- Orlando Clinical Research Center - Orlando
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2020-01-06 |
| Est. Completion | 2020-12-14 |
| Phase | Phase 1 |
What the finished NCT06094725 record still lists
NCT06094725 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 36-participant average among 48 other Hepatic Impairment trials with a reported enrollment target (17% lower).
The record links to 1 condition, with Hepatic Impairment appearing as the primary indexed condition, and to 1 intervention - of which Relacorilant is the first listed.
NCT06094725 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT06094725 about?
NCT06094725 is a clinical study titled "A Study to Evaluate the Effects of Hepatic Impairment on the Pharmacokinetics of Relacorilant". The primary objective of this multiple-dose, adaptive design study is to evaluate the effect of hepatic impairment on the pharmacokinetics (PK) of relacorilant relative to healthy matched control male and female subjects (Part 1).
What is the current status of trial NCT06094725?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2020-01-06. Estimated completion is 2020-12-14.
What conditions does trial NCT06094725 study?
This clinical trial studies the following conditions: Hepatic Impairment.
What interventions are being tested in trial NCT06094725?
The interventions under investigation include: Relacorilant (DRUG).
Who is sponsoring clinical trial NCT06094725?
This trial is sponsored by Corcept Therapeutics, which has 54 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06094725 being conducted?
This trial has 2 study locations across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hepatic Impairment
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06094725's enrollment target sits among peer trials
30 21st of 48 higher than 24 of 48 other Hepatic Impairment trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hepatic Impairment trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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