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Congenital Disorder of Glycosylation
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Congenital Disorder of Glycosylation trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which Congenital Disorder of Glycosylation trials may be worth asking aboutNorth America
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The primary objective of this study is to evaluate the safety and tolerability of the dietary supplement, nicotinamide mononucleotide (NMN), in individuals with…
Background: \- Proteins, fats, and other molecules are the body s building blocks. Many of these molecules must have sugars, or chains of sugars, attached to w…
The purpose of this research is to study the natural history of congenital disorders of glycosylation and its causes and treatments.
The Congenital Muscle Disease Patient and Proxy Reported Outcome Study (CMDPROS) is a longitudinal 10 year study to identify and trend care parameters, adverse…
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-C…
The aim of the study is to evaluate the role of the endothelial barrier in the occurrence of stroke-like episode. And to study the protein C system on the surfa…