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NCT00775359 · ClinicalTrials.gov registry record · NA

Bioequivalence Study of Fenofibrate 160mg Tablets Under Fed Conditions

A NA study, sponsored by Ranbaxy Laboratories Limited.

Completed
Registry status
NA
Development phase
24
Enrollment target

NCT00775359: Completed NA study, sponsored by Ranbaxy Laboratories Limited.

NCT00775359 is a NA study that has completed, run by Ranbaxy Laboratories Limited. The registered enrollment target is 24 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00775359, a NA study, has completed, sponsored by Ranbaxy Laboratories Limited.

COMPLETED
Registry status
NA
Development phase
24 participants
Enrollment target

Study Summary

The objective of this study was to compare the single-dose relative bioavailability of Ranbaxy and Abbott (TriCor) 160 mg fenofibrate tablets under fed conditions.

Interventions

  • DRUG Fenofibrate 160 mg tablets

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2002-08
Est. Completion 2002-10
Phase NA
Ranbaxy Laboratories Limited

44 total trials

What the finished NCT00775359 record still lists

NCT00775359 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which Fenofibrate 160 mg tablets is the first listed.

NCT00775359 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00775359 about?

NCT00775359 is a clinical study titled "Bioequivalence Study of Fenofibrate 160mg Tablets Under Fed Conditions". The objective of this study was to compare the single-dose relative bioavailability of Ranbaxy and Abbott (TriCor) 160 mg fenofibrate tablets under fed conditions.

What is the current status of trial NCT00775359?

This trial is currently completed. It is a NA study. The enrollment target is 24 participants. The study started on 2002-08. Estimated completion is 2002-10.

What interventions are being tested in trial NCT00775359?

The interventions under investigation include: Fenofibrate 160 mg tablets (DRUG).

Who is sponsoring clinical trial NCT00775359?

This trial is sponsored by Ranbaxy Laboratories Limited, which has 44 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00775359's enrollment target sits among peer trials

24 1736th of 2000 higher than 246 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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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Source: ClinicalTrials.gov NCT00775359, the US trial registry maintained by the National Library of Medicine. NCT00775359 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.