About 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form
3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form is a rare disease catalogued by Orphanet (ORPHA:79351). It is associated with the PHGDH gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form trials.
Search ClinicalTrials.gov for "3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form" or filter by Orphanet code ORPHA:79351 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form. Updated daily.