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NCT00141817 · ClinicalTrials.gov registry record · Phase 3

Study Evaluating Pantoprazole in Children With GERD

A Phase 3 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Completed
Registry status
Phase 3
Development phase
41
Enrollment target

NCT00141817 is a Phase 3 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 41 participants.

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The verdict

NCT00141817, a Phase 3 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 3
Development phase
41 participants
Enrollment target

Study Summary

The purpose of this study is to characterize the PK profile, safety and tolerability of single and multiple doses of pantoprazole in children aged 1 through 11 years with endoscopically proven GERD.

Interventions

  • DRUG pantoprazole for approximately 9 weeks.

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2005-08
Est. Completion 2007-11
Phase Phase 3

What the Registry Record Tells You About NCT00141817

The ClinicalTrials.gov registry entry for NCT00141817 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which pantoprazole for approximately 9 weeks. is the first listed.

NCT00141817 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00141817 about?

NCT00141817 is a clinical study titled "Study Evaluating Pantoprazole in Children With GERD". The purpose of this study is to characterize the PK profile, safety and tolerability of single and multiple doses of pantoprazole in children aged 1 through 11 years with endoscopically proven GERD.

What is the current status of trial NCT00141817?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 41 participants. The study started on 2005-08. Estimated completion is 2007-11.

What interventions are being tested in trial NCT00141817?

The interventions under investigation include: pantoprazole for approximately 9 weeks. (DRUG).

Who is sponsoring clinical trial NCT00141817?

This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.

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.