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NCT03824678 · ClinicalTrials.gov registry record · Phase 1
Evaluate the Pharmacokinetics of CC-220 in Subjects With Mild, Moderate, or Severe Hepatic Impairment Compared With Healthy Subjects
A Phase 1 study, sponsored by Celgene.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT03824678 is a Phase 1 study that has completed, run by Celgene. The registered enrollment target is 40 participants.
The verdict
NCT03824678, a Phase 1 study, has completed, sponsored by Celgene.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
This is a multicenter, open-label study to assess the PK of a single 1-mg oral dose of CC-220 in subjects with mild, moderate, and severe hepatic impairment, and in matched healthy control subjects with normal hepatic function. Degree of hepatic impairment will be determined during the Screening period by the subject's score according to Child-Pugh Classification Criteria
Interventions
- DRUG CC-220
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2019-02-13 |
| Est. Completion | 2019-06-18 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03824678
The ClinicalTrials.gov registry entry for NCT03824678 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Celgene, which has 308 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which CC-220 is the first listed.
NCT03824678 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03824678 about?
NCT03824678 is a clinical study titled "Evaluate the Pharmacokinetics of CC-220 in Subjects With Mild, Moderate, or Severe Hepatic Impairment Compared With Healthy Subjects". This is a multicenter, open-label study to assess the PK of a single 1-mg oral dose of CC-220 in subjects with mild, moderate, and severe hepatic impairment, and in matched healthy control subjects with normal hepatic function. Degree of hepatic impairment will be determined during the Screening pe...
What is the current status of trial NCT03824678?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2019-02-13. Estimated completion is 2019-06-18.
What interventions are being tested in trial NCT03824678?
The interventions under investigation include: CC-220 (DRUG).
Who is sponsoring clinical trial NCT03824678?
This trial is sponsored by Celgene, which has 308 total clinical trials registered on ClinicalTrials.gov.
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