Viewing Gene With Clinical Trials Data

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Gene Data From HGNC: https://www.genenames.org/download/statistics-and-files/
Symbol: PHOX2B
Name: paired like homeobox 2B
Location: 04p13
Locus Group: protein-coding gene
Gene Type: Protein Coding
Locus Type: gene with protein product
ID+ Clinical Trials CompTox DrugMatrix Conditions Design Enrollment Locations Outcomes
Clinical Trials Data: https://classic.clinicaltrials.gov/api/gui/ref/download_all

Clinical Studies

NCT Number Status Brief Title View
NCT03568669 Neurocognition in Congenital Central Hypoventilation Syndrome CCHS View
NCT01225679 Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene View
NCT00652964 PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family Presentations From Newborn to Adulthood View
NCT03088020 International Congenital Central Hypoventilation Syndrome CCHS Registry and CCHS SHARE View