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NCT06710366: DAO-NEO-2022

Prevalence of DAO (diamino Oxidase) Deficiency in Newborns

Completed Last updated 29 November 2024
What this trial tests

trial in DAO Genetic Variants in 200 participants. Completed in 26 June 2024.

Timeline
28 February 2023
Primary endpoint
21 June 2024
26 June 2024

Quick facts

Lead sponsorAB Biotek
StatusCompleted
Study typeOBSERVATIONAL
Enrollment200
Start date28 February 2023
Primary completion21 June 2024
Estimated completion26 June 2024
Sites1 location across Spain

Conditions studied

Sponsor

AB Biotek

Who can join

Adults 0 Days to 3 Days, any sex, with DAO Genetic Variants. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Observational study to estimate the prevalence of genetic DAO deficiency in the population.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The Prevalence of Single Nucleotide Polymorphisms of the <i>AOC1</i> Gene Associated with Diamine Oxidase (DAO) Enzyme Deficiency in Healthy Newborns: A Prospective Population-Based Cohort Study.
    Fortes Marin E, Carrera Marcolin L, Martí Melero L, Tintoré Gazulla M, et al · · 2025 · cited 4× · PMID 40004469 · DOI 10.3390/genes16020141

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Other AB Biotek trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06710366.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing