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TERMINATED
NCT05228184
PHASE4

Use of Tirosint®-SOL or Tablet Formulations of Levothyroxine in Pediatric Patients With Congenital Hypothyroidism (CH)

Sponsor: IBSA Institut Biochimique SA

View on ClinicalTrials.gov

Summary

This is a multi-center, prospective, parallel-group, open-label, randomized clinical study in one hundred and twenty-six (126) neonates and infants diagnosed with CH. Subjects will be randomized in a 2:1 ratio to Treatment (Tirosint®-SOL) or Control (conventional therapy with levothyroxine sodium crushed tablets).

Official title: A Randomized Comparative Study Between Liquid (Tirosint®-SOL) and Tablet Formulations of Levothyroxine in Neonates and Infants With Congenital Hypothyroidism

Key Details

Gender

All

Age Range

1 Day - 9 Months

Study Type

INTERVENTIONAL

Enrollment

34

Start Date

2022-01-21

Completion Date

2025-03-27

Last Updated

2026-05-29

Healthy Volunteers

No

Interventions

DRUG

Tirosint®-SOL

Dosage will be according to the USPI and Standard of Care.

DRUG

Levothyroxine Sodium

Tablets will be crushed and dissolved in solution. Dosage will be according to the USPI and Standard of Care.

Locations (10)

Children's Hospital of Los Angeles

Los Angeles, California, United States

CHOC Children's Hospital

Orange, California, United States

University of California San Francisco

San Francisco, California, United States

Yale University

New Haven, Connecticut, United States

Children's Hospital of Atlanta

Atlanta, Georgia, United States

Ann & Robert H. Lurie Children's Hospital of Chicago

Chicago, Illinois, United States

Boston Children's Hospital

Boston, Massachusetts, United States

Children's Mercy Hospital and Clinics

Kansas City, Missouri, United States

Children's Hospital Medical Center

Cincinnati, Ohio, United States

Cook Children's Health Care Systems

Fort Worth, Texas, United States