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Results for “Congenital Disorders of Glycosylation”

Showing 3 of 0 results

Not applicableLooking for participantsNCT01403402
What this trial is testing

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

Who this might be right for
Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) DeficiencyAlpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)+49 more
Cure CMD 4,000
Testing effectiveness (Phase 2)Enrolling By InvitationNCT06657859
What this trial is testing

Open-Label Extension Study to Assess GLM101 in PMM2-CDG Patients

Who this might be right for
Pmm2-CDGPhosphomannomutase 2 Deficiency
Glycomine, Inc. 90
Testing effectiveness (Phase 2)Not Yet RecruitingNCT05402332
What this trial is testing

Evaluating the Efficacy and Safety of D-galactose in PGM1-CDG (AVTX-801)

Who this might be right for
PGM1-CDG - Phosphoglucomutase 1-Related Congenital Disorder of Glycosylation
Eva Morava-Kozicz 8

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