Inborn disorder of pyridoxine metabolism
MONDO:0019237An inherited metabolic disease that is has its basis in the disruption of pyridoxine metabolic process.
Also known as: inborn error of pyridoxine metabolic process, inborn pyridoxine metabolic process disorder, rare inborn error of pyridoxine metabolic process, disorder of pyridoxine metabolism
4 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Broader categories
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Cialis and keytruda together against head and neck cancer: small trial shows promise?
Disease control CompletedThis completed phase II study tested a combination of two drugs—tadalafil (Cialis) and pembrolizumab (Keytruda)—in 7 adults with advanced head and neck cancer that had spread or come back. The goal was to see if the combination was safe and could help control the disease. Because…
Phase 2 • Sponsor: University of California, San Diego • Aim: Disease control
Last updated Jun 27, 2026 09:04 UTC
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Can a special diet shape brain development in a rare epilepsy?
Knowledge-focused CompletedThis study looks at how children over age 3 with pyridoxine-dependent epilepsy, a rare genetic condition, develop cognitively over time. Researchers will use a standardized questionnaire called Vineland II to measure adaptive behaviors like communication and daily living skills. …
Sponsor: University Hospital, Angers • Aim: Knowledge-focused
Last updated Aug 12, 2026 00:00 UTC