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NCT00808678 · ClinicalTrials.gov registry record · Phase 1
Comparison of the Bioavailability of Fenofibric Acid and Rosuvastatin From ABT-143 Relative to That From the Coadministration of ABT-335 (Fenofibric Acid) and Rosuvastatin Calcium
A Phase 1 study, sponsored by AstraZeneca.
- Completed
- Registry status
- Phase 1
- Development phase
- 90
- Enrollment target
NCT00808678 is a Phase 1 study that has completed, run by AstraZeneca. The registered enrollment target is 90 participants.
The verdict
NCT00808678, a Phase 1 study, has completed, sponsored by AstraZeneca.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 90 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety and compare the pharmacokinetic parameters from the fixed dose combination ABT-143 relative to that from the co-administration of the two monotherapies.
Interventions
- DRUG rosuvastatin
- DRUG ABT-335
- DRUG ABT-143
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2008-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00808678
The ClinicalTrials.gov registry entry for NCT00808678 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which rosuvastatin is the first listed.
NCT00808678 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00808678 about?
NCT00808678 is a clinical study titled "Comparison of the Bioavailability of Fenofibric Acid and Rosuvastatin From ABT-143 Relative to That From the Coadministration of ABT-335 (Fenofibric Acid) and Rosuvastatin Calcium". The purpose of this study is to evaluate the safety and compare the pharmacokinetic parameters from the fixed dose combination ABT-143 relative to that from the co-administration of the two monotherapies.
What is the current status of trial NCT00808678?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 90 participants. The study started on 2008-12.
What interventions are being tested in trial NCT00808678?
The interventions under investigation include: rosuvastatin (DRUG), ABT-335 (DRUG), ABT-143 (DRUG).
Who is sponsoring clinical trial NCT00808678?
This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.
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