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Completed Phase 1 Interventional Results available

A Study to Evaluate Vonoprazan in Children Who Have Symptomatic Gastroesophageal Reflux Disease

ClinicalTrials.gov ID: NCT06106022

Public ClinicalTrials.gov record NCT06106022. 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 21, 2026, 1:36 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 Phase 1, Randomized, Parallel-group, Open-label, Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety of Vonoprazan (10 or 20 mg Once Daily) in Children Aged ≥ 6 to < 12 Years Who Have Symptomatic Gastroesophageal Reflux Disease

Brief summary

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

The aim of this study is to evaluate the pharmacokinetic (PK) profile of vonoprazan (10 or 20 mg once daily \[QD\]) in children ≥ 6 to \< 12 years of age who have symptomatic Gastroesophageal Reflux Disease (GERD).

Study identification

NCT ID
NCT06106022
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Phathom Pharmaceuticals, Inc.
Industry
Enrollment
22 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 Years to 11 Years
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 1, 2023 (Actual)
Primary completion
Apr 16, 2024 (Actual)
Completion
Apr 29, 2024 (Actual)
Last update posted
Dec 19, 2024

2023 – 2024

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Strada Patient Care Center Mobile Alabama 36604 —
Preferred Research Partners, Inc. Little Rock Arkansas 72211 —
Med Research Associates, Inc Hollywood Florida 33024 —
Avanza Medical Research Center Pensacola Florida 32503 —
International Center for Research Tampa Florida 33614 —
Children's Center for Digestive Health Care, LLC Atlanta Georgia 30342 —
Riley Hospital for Children at IU Health Indianapolis Indiana 46202 —
Tandem Clinical Research GI, LLC Marrero Louisiana 70072 —
Advantage Clinical Trials The Bronx New York 10467 —
PriMED Clinical Research Dayton Ohio 45429 —
Cyn3rgy Research Gresham Oregon 97030 —
Maspons Pediatric Gastro El Paso Texas 79902 —
Stryde Research - NxT Step Pediatrics Frisco Texas 75033 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06106022, 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 Dec 19, 2024 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06106022 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →