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

Find clinical trials for slc35a2-cdg - solute carrier family 35 member a2 congenital disorder of glycosylation. Discover research opportunities and treatment options in your area.

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AVTX-801 D-galactose Supplementation in SLC35A2-CDG

NCT ID: NCT05402384

This clinical trial is studying a treatment called AVTX-801 for individuals with a rare genetic condition known as SLC35A2-CDG, which can cause various health issues like seizures and digestive pro...

Not yet recruiting

Phase: PHASE2 Type: interventional Locations: Rochester, Minnesota, United States

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