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NCT00917579 · ClinicalTrials.gov registry record · Phase 4

Bioequivalence Study Comparing A New 10 Mg Atorvastatin Tablet To A 10 Mg Atorvastatin Commercial Tablet

A Phase 4 study of Hypercholesterolemia, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

Completed
Registry status
Phase 4
Development phase
76
Enrollment target
1
Study location

NCT00917579 is a Phase 4 study of Hypercholesterolemia that has completed, run by Pfizer's Upjohn has merged with Mylan to form Viatris. The registered enrollment target is 76 participants, below the 816-participant average among 62 other Hypercholesterolemia trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00917579, a Phase 4 study of Hypercholesterolemia, has completed, sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris.

COMPLETED
Registry status
Phase 4
Development phase
76 participants
Enrollment target
1
Study location

Study Summary

• To determine whether new 10 mg atorvastatin tablets are bioequivalent to 10 mg commercial atorvastatin tablets (Lipitor®).

Conditions Studied

Interventions

  • DRUG Atorvastatin

Study Locations (1)

Florida

  • Pfizer Investigational Site - Miami

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2008-07
Est. Completion 2008-09
Phase Phase 4

What the Registry Record Tells You About NCT00917579

The ClinicalTrials.gov registry entry for NCT00917579 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 816-participant average among 62 other Hypercholesterolemia trials with a reported enrollment target (91% lower). The listed sponsor is Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hypercholesterolemia appearing as the primary indexed condition, and to 1 intervention - of which Atorvastatin is the first listed.

NCT00917579 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.

Frequently Asked Questions

What is clinical trial NCT00917579 about?

NCT00917579 is a clinical study titled "Bioequivalence Study Comparing A New 10 Mg Atorvastatin Tablet To A 10 Mg Atorvastatin Commercial Tablet". • To determine whether new 10 mg atorvastatin tablets are bioequivalent to 10 mg commercial atorvastatin tablets (Lipitor®).

What is the current status of trial NCT00917579?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 76 participants. The study started on 2008-07. Estimated completion is 2008-09.

What conditions does trial NCT00917579 study?

This clinical trial studies the following conditions: Hypercholesterolemia.

What interventions are being tested in trial NCT00917579?

The interventions under investigation include: Atorvastatin (DRUG).

Who is sponsoring clinical trial NCT00917579?

This trial is sponsored by Pfizer's Upjohn has merged with Mylan to form Viatris, which has 158 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00917579 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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