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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of GlcNAc on Tear Production in NGLY1-CDDGcongenital disorder of deglycosylation 1Active, not recruitingPhase 22026-09-29NCT05402345
AVTX-801 D-galactose Supplementation in SLC35A2-CDGSLC35A2-CDG - Solute Carrier Family 35 Member A2 Congenital Disorder of GlycosylationNot yet recruitingPhase 22026-06-29NCT05402384
Assessing the Safety and Tolerability of NMN in DHDDS-CDGCongenital, Hereditary, and Neonatal Diseases and Abnormalities, DHDDS-CDG, Nutritional and Metabolic Diseases, congenital disorder of glycosylation, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, metabolic diseaseRecruitingPhase 12026-06-22NCT07572825
Evaluating the Efficacy and Safety of D-galactose in PGM1-CDG (AVTX-801)PGM1-congenital disorder of glycosylationNot yet recruitingPhase 22026-03-16NCT05402332