Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Evaluate the Safety and Efficacy of Ferric Maltol Oral Suspension vs. Ferrous Sulfate Oral Liquid in Children and Adolescents Aged 2 to 17 Years With Iron-deficiency Anaemia, With a Single Arm Study in Infants Aged 1 Month to Less Than 2 Years

ClinicalTrials.gov ID: NCT05126901

Public ClinicalTrials.gov record NCT05126901. 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 Jul 21, 2026, 12:54 PM EDT

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

Official title

Randomised, Open-label, Active-controlled, Multicentre, Comparative Study to Evaluate the Safety and Efficacy of Ferric Maltol (Iron (III)-Maltol Complex) (ST10) Oral Suspension Compared to Ferrous Sulfate Oral Liquid in Children and Adolescents Aged 2 to 17 Years With Iron-deficiency Anaemia, Incorporating a Single Arm Study in Infants Aged 1 Month to Less Than 2 Years

Study identification

NCT ID
NCT05126901
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Shield Therapeutics
Industry
Enrollment
65 participants

Conditions and interventions

Interventions

  • Ferric Maltol Drug
  • Ferrous sulfate Drug

Drug

Eligibility (public fields only)

Age range
1 Month to 17 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 2, 2021
Primary completion
Jun 8, 2024
Completion
Jun 8, 2024
Last update posted
Nov 9, 2025

2021 – 2024

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
The Center for Clinical Trials Saraland Alabama 36571
Homestead Research Institute Homestead Florida 33030
Kissimmee Clinical Research Corp Kissimmee Florida 34743
Miami Clinical Research Miami Florida 33155
Medical Research of Westcheste Miami Florida 33165
Eminent Clinical Research and Associates North Lauderdale Florida 33068
Clinical Research Prime Idaho Falls Idaho 83404
Sierra Clinical Research Las Vegas Nevada 89106
Levine Cancer Institute Charlotte North Carolina 28204
Penn State Hershey Children's Hospital Hershey Pennsylvania 17033
Hasbro Children's Hospital Providence Rhode Island 02903
BRCR Global Texas Edinburg Texas 78539
Zion Research Katy Texas 77494
MultiCare Health System Institute for Research and Innovation Tacoma Washington 98405

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 9 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05126901, 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 Nov 9, 2025 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05126901 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →