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NCT00810758 · ClinicalTrials.gov registry record · Phase 1

Multiple Oral Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of PF-04878691

A Phase 1 study of Hepatitis C Virus, sponsored by Pfizer.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target
1
Study location

NCT00810758 is a Phase 1 study of Hepatitis C Virus that has completed, run by Pfizer. The registered enrollment target is 24 participants, below the 310-participant average among 3 other Hepatitis C Virus trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00810758, a Phase 1 study of Hepatitis C Virus, has completed, sponsored by Pfizer.

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

Study Summary

To assess the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple oral doses of PF-04878691.

Conditions Studied

Interventions

  • DRUG PF-04878691 3mg
  • DRUG PF-04878691 6mg
  • DRUG PF-04878691 9mg

Study Locations (1)

Connecticut

  • Pfizer Investigational Site - New Haven

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2009-01
Est. Completion 2009-11
Phase Phase 1

Sponsor

Pfizer

1,845 total trials

What the Registry Record Tells You About NCT00810758

The ClinicalTrials.gov registry entry for NCT00810758 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 310-participant average among 3 other Hepatitis C Virus trials with a reported enrollment target (92% lower). The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hepatitis C Virus appearing as the primary indexed condition, and to 3 interventions - of which PF-04878691 3mg is the first listed.

NCT00810758 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT00810758 about?

NCT00810758 is a clinical study titled "Multiple Oral Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of PF-04878691". To assess the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple oral doses of PF-04878691.

What is the current status of trial NCT00810758?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2009-01. Estimated completion is 2009-11.

What conditions does trial NCT00810758 study?

This clinical trial studies the following conditions: Hepatitis C Virus.

What interventions are being tested in trial NCT00810758?

The interventions under investigation include: PF-04878691 3mg (DRUG), PF-04878691 6mg (DRUG), PF-04878691 9mg (DRUG).

Who is sponsoring clinical trial NCT00810758?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00810758 being conducted?

This trial has 1 study location across Connecticut. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.