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Completed Phase 3 Interventional Results available

Study Evaluating Pantoprazole Sodium Enteric-Coated Spheroid Suspension In Infants With Presumed GERD

ClinicalTrials.gov ID: NCT00259012

Public ClinicalTrials.gov record NCT00259012. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 5:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Open Label, Single and Multiple Dose Study of the Pharmacokinetics and Pharmacodynamics of 2 Dose Levels of Pantoprazole Sodium Enteric-Coated Spheroid Suspension in Infants Aged 1 Through 11 Months With Presumed GERD

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to characterize the pharmacokinetic (PK) and pharmacodynamic (PD) profiles to determine the safety and tolerability of single and multiple doses of pantoprazole in infants aged 1 through 11 months.

Study identification

NCT ID
NCT00259012
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
67 participants

Conditions and interventions

Eligibility (public fields only)

Age range
1 Month to 11 Months
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2005 (Type not available)
Primary completion
Mar 2008 (Actual)
Completion
Mar 2008 (Actual)
Last update posted
May 7, 2010

2005 – 2008

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Not listed Little Rock Arkansas 72205 —
Not listed Loma Linda California 92351 —
Not listed San Diego California 92103 —
Not listed Washington D.C. District of Columbia 20010 —
Not listed Miami Florida 33101 —
Not listed Pensacola Florida 32504 —
Not listed Chicago Illinois 60614 —
Not listed Park Ridge Illinois 60068 —
Not listed Louisville Kentucky 40202 —
Not listed Shreveport Louisiana 71130 —
Not listed Jackson Mississippi 39216 —
Not listed Kansas City Missouri 64108 —
Not listed New York New York 10032 —
Not listed Durham North Carolina 27710 —
Not listed Cleveland Ohio 44106 —
Not listed Temple Texas 76508 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00259012, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 7, 2010 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00259012 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →