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Study identifier: NCT05480761 Synced from ClinicalTrials.gov · July 27, 2026
● Terminated

7-Day Trial of Sucraid for Alleviating CSID Symptoms in Subjects With Low, Moderate, and Normal Sucrase Levels

Condition: Congenital Sucrase-Isomaltase Deficiency · CSID · Sucrase Isomaltase Deficiency  ·  Sponsor: QOL Medical, LLC

PhasePhase 4
Planned participants312
Who can joinAll sexes, 6 Months to 17 Years
Healthy volunteersNo

About this study

This is a Phase 4, U.S. only, multi-center study using a 7-day therapeutic response dose (TRD) of commercial Sucraid® to assess the response of treatment in 1100 symptomatic pediatric (6 months to 17 years old) subjects with low, moderate, and normal sucrase activity determined by a disaccharidase assay via EGD within 1 year of the Screening Visit. This study will also explore the relationship between known genetic CSID mutations and sucrase activities via (EGD) disaccharidase assay (low, moderate, and normal).

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (20)

Children's Hospital Los AngelesLos Angeles, California, United States
UCSF Benioff Children's Hospital OaklandOakland, California, United States
Kidz MedicalCoral Gables, Florida, United States
Orlando HealthOrlando, Florida, United States
Children's Healthcare of AtlantaAtlanta, Georgia, United States
Center for Digestive Health Care, LLCAtlanta, Georgia, United States
University of Maryland BaltimoreBaltimore, Maryland, United States
Johns Hopkins UniversityBaltimore, Maryland, United States
GI AssociatesFlowood, Mississippi, United States
Happy TummiesFlowood, Mississippi, United States
Children's Mercy HospitalKansas City, Missouri, United States
Atlantic Health SystemMorristown, New Jersey, United States

+ 8 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05480761