Congenital sucrase-isomaltase deficiency

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At a Glance

Live from database

Regulatory Watchboard

4 events
Feb 2026Sucrase-Isomaltase (SI) Genes and Meal Load

Region Skane — NA

TrialNOT YET RECRUITING
Mar 2025Genetic Carbohydrate Maldigestion As Model to Study Food Hypersensitivity Mechanism (WORK PACKAGE 2)

University of Nottingham

TrialNOT YET RECRUITING
Mar 2022Sucrase-isomaltase Deficiency as a Cause of Irritable Bowel Syndrome

Lovisenberg Diakonale Hospital — NA

TrialNOT YET RECRUITING
Apr 1998

Sucraid: FDA approved

Oral replacement therapy of the genetically determined sucrase deficiency, which is part of congenital sucrease-isomaltase deficiency.

FDAcompleted

Data from FDA regulatory filings and ClinicalTrials.gov. Updated periodically.

Financial Assistance

1 program

FINANCIAL LANDSCAPE SUMMARY

1

Total programs

1

Open now

Patient Assistance Programs1

Sucraid

QOL Medical, LLC

OpenContact for detailsApply ↗

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Approved Treatments

3 FDA-approved

Sucraid

(Sacrosidase)Orphan drug

QOL Medical, LLC

Sucrose-specific Enzyme [EPC]

Approved Apr 1998FDA label ↗

Normocarb HF

(bicarbonate infusate)Orphan drugstandard

Dialysis Solutions, Inc.

Cimetidine

(CIMETIDINE)Orphan drugstandard

Chartwell RX, LLC

Histamine-2 Receptor Antagonist [EPC]

FDA label ↗

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Clinical Trial Landscape

No active clinical trials currently recruiting for Congenital sucrase-isomaltase deficiency.
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Recent News & Research

No recent news articles indexed yet for Congenital sucrase-isomaltase deficiency.
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Specialist Network

Top 6 by expertise

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