Last reviewed · How we verify
NCT06710366: DAO-NEO-2022
Prevalence of DAO (diamino Oxidase) Deficiency in Newborns
trial in DAO Genetic Variants in 200 participants. Completed in 26 June 2024.
21 June 2024
Quick facts
| Lead sponsor | AB Biotek |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 200 |
| Start date | 28 February 2023 |
| Primary completion | 21 June 2024 |
| Estimated completion | 26 June 2024 |
| Sites | 1 location across Spain |
Conditions studied
- DAO Genetic Variants — all drugs for DAO Genetic Variants →
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):
-
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
Verify or expand the search:
- PubMed search for NCT06710366
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other AB Biotek trials
Trials by the same sponsor.
- NCT06715163 — Evaluation of the Safety and Tolerability of Three Doses of Diamine Oxidase (DAO) in Healthy Volunteers · NA · completed
- NCT07027943 — Evaluation Of The Diamine Oxidase Supplementation Effect In Patients With Insomnia Symptoms · NA · completed
- NCT07006558 — Kinetic Study Of Supplementation With The Enzyme Diamine Oxidase In Patients With Histamine Intolerance · NA · completed
- NCT06488027 — DAO DEFICIENCY SCREENING AMONG PATIENTS WITH INSOMNIA SYMPTOMS · completed
- NCT06738433 — Efficacy and Tolerability of ABB I5 Prebiotic and ABB C22 Postbiotics for the Management of Constipation and Gastrointes · EARLY_PHASE1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06710366 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by AB Biotek
- Last refreshed: 29 November 2024
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