Clin2
NCT05402384Possibly a fitNot yet recruiting

D-galactose supplement for SLC35A2-CDG symptoms

SLC35A2-CDG - Solute Carrier Family 35 Member A2 Congenital Disorder of Glycosylation

Part of Genetic & congenital, Hormones & metabolism clinical trials.

This study tests a sugar called D-galactose given as a supplement to help with symptoms of SLC35A2-CDG, a rare genetic condition that can cause seizures and digestive problems. The goal is to see if taking this sugar improves those symptoms.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
10 people
Ages
1 month and older
Study type
Interventional

Who can take part

  • Confirmed change in the SLC35A2 gene from a genetic test
  • Patient is older than 1 month
  • Has at least one of these symptoms: seizures, chronic vomiting, chronic constipation, or chronic diarrhea
  • A parent or guardian can give permission (for minors or adults who can't consent)
  • Females over age 8 must use birth control
  • Had an eye exam within the past year
  • Cannot have galactosemia or aldolase-B deficiency, and must not have had serious reactions to galactose before

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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