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

Tundra lists 1 SLC35A2-CDG - Solute Carrier Family 35 Member A2 Congenital Disorder of Glycosylation clinical trial. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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NOT YET RECRUITING

NCT05402384

AVTX-801 D-galactose Supplementation in SLC35A2-CDG

This is a multicenter, randomized, double-blind, placebo-controlled, cross-over study to evaluate the efficacy and safety of AVTX-801 in subjects with SLC35A2-CDG

Gender: All

Ages: 1 Month - Any

Updated: 2025-06-29

1 state

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