Clin2
NCT05402332Possibly a fitNot yet recruiting

D-galactose study for PGM1-CDG

PGM1-CDG - Phosphoglucomutase 1-Related Congenital Disorder of Glycosylation

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

This study tests a sugar called D-galactose to see if it is safe and works well for people with PGM1-CDG, a rare genetic condition that affects how the body uses sugar. If you are already taking D-galactose, this trial will check if it helps your symptoms.

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

Phase
Phase 2
Enrollment
8 people
Ages
18 years to 60 years
Study type
Interventional

Who can take part

  • You are between 18 and 60 years old.
  • You have been diagnosed with PGM1-CDG through genetic testing.
  • You are currently taking a stable dose of D-galactose.
  • You are not pregnant or breastfeeding, and you agree to use effective birth control if needed.
  • You do not have certain other conditions like aldolase B deficiency, galactosemia, or severe anemia.
  • You have not had severe reactions to galactose in the past, such as severe diarrhea or vomiting.

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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