Autosomal recessive GTP cyclohydrolase deficiency Clinical Trials

3 clinical trials for Autosomal recessive GTP cyclohydrolase deficiency across international registries, including 3 currently recruiting participants. Compare status, phase, eligibility criteria and locations.

• iNTD (International Network on Neurotransmitter related Disorders) Registry — RECRUITING
• Investigation of the underlying pathomechanisms found in defects of the neurotransmitter, Pterine -, phenyl alanine, and 5-Methyltetrahydrofolate metabolism in induced pluripotent stem cells (iPSC) and derivatives — RECRUITING
• Pathophysiology of L-Dopa responsive Dystonia and other monogenetic disorders — RECRUITING

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