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NCT00960856 · ClinicalTrials.gov registry record · Phase 1
Four Arm Food Effect Study of Fenofibric Acid Tablets
A Phase 1 study, sponsored by Mutual Pharmaceutical Company.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
NCT00960856: Completed Phase 1 study, sponsored by Mutual Pharmaceutical Company.
NCT00960856 is a Phase 1 study that has completed, run by Mutual Pharmaceutical Company. The registered enrollment target is 40 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00960856, a Phase 1 study, has completed, sponsored by Mutual Pharmaceutical Company.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
Study Summary
The primary objective of this study is to characterize the single-dose pharmacokinetic profile of fenofibric acid (105 mg tablets) and the effect of food of various calorie/fat compositions on the rate and extent of absorption. Additionally, the safety and tolerability of this dose and regimen of fenofibric acid will be evaluated.
Primary Outcome
The maximum or peak concentration that the drug reaches in the plasma.
Interventions
- DRUG Fenofibric Acid 105 mg Tablet
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2007-11 |
| Est. Completion | 2007-11 |
| Phase | Phase 1 |
What the finished NCT00960856 record still lists
NCT00960856 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (33% lower).
The record links to 0 conditions, and to 1 intervention - of which Fenofibric Acid 105 mg Tablet is the first listed.
NCT00960856 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00960856 about?
NCT00960856 is a clinical study titled "Four Arm Food Effect Study of Fenofibric Acid Tablets". The primary objective of this study is to characterize the single-dose pharmacokinetic profile of fenofibric acid (105 mg tablets) and the effect of food of various calorie/fat compositions on the rate and extent of absorption. Additionally, the safety and tolerability of this dose and regimen of fe...
What is the current status of trial NCT00960856?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2007-11. Estimated completion is 2007-11.
What interventions are being tested in trial NCT00960856?
The interventions under investigation include: Fenofibric Acid 105 mg Tablet (DRUG).
Who is sponsoring clinical trial NCT00960856?
This trial is sponsored by Mutual Pharmaceutical Company, which has 27 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00960856's enrollment target sits among peer trials
40 1130th of 2000 higher than 810 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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.
Source ClinicalTrials.gov registry export · 2026-08-08
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