Clin2
NCT07572825Possibly a fitRecruiting

Safety study of NMN supplement for DHDDS-CDG

DHDDS-Congenital Disorder of GlycosylationDHDDS-CDGCongenital Disorder of Glycosylation

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

This trial tests whether a supplement called NMN is safe and well-tolerated in children and adults with a rare genetic condition called DHDDS-CDG. NMN may help support cellular energy and protein production, which are affected by this condition.

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

Phase
Phase 1
Enrollment
8 people
Ages
4 years and older
Study type
Interventional

Who can take part

  • You are at least 4 years old
  • You have been diagnosed with DHDDS-CDG (a rare genetic disorder affecting sugar processing) through genetic testing
  • You do not have moderate or severe intellectual disability (IQ below 52)
  • Your liver and kidney function are adequate (no liver failure, ALT/AST less than 5× normal, eGFR above 30)
  • You are not pregnant and not currently in another experimental drug trial
  • You are not taking aspirin, metformin, or cholesterol-lowering medications (statins)

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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