Drugs / Luvadaxistat
Trials 11
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 17 trials | ||||||
| Phase 1 | NCT04234672 | Feb → Apr 2020 | — | Neurocrine Biosciences | Completed | No outcome recorded |
| Phase 1 | NCT03706469 | Oct → Dec 2018 | — | Neurocrine Biosciences | Completed | No outcome recorded |
| Phase 1 | NCT03687684 | Oct 2018 → Jun 2019 | — | Neurocrine Biosciences | Completed | No outcome recorded |
| Phase 1 | NCT03224325 | Jul 2017 → Sep 2018 | — | Neurocrine Biosciences | Completed | No outcome recorded |
| Phase 1 | NCT03101293 | Apr → May 2017 | — | Neurocrine Biosciences | Completed | No outcome recorded |
| Phase 1 | NCT02716987 | Mar → Aug 2016 | — | Neurocrine Biosciences | Completed | No outcome recorded |
| Phase 1 | NCT02566759 | Sep 2015 → Jun 2016 | — | Neurocrine Biosciences | Terminated | No outcome recorded |
| Phase 24 trials · 4 missed | ||||||
| Phase 2 | NCT05182476 | Dec 2021 → Jun 2024 | schizophrenia | Neurocrine Biosciences | Terminated | Missed primary |
| Phase 2 | NCT03359785 | Jan 2018 → Dec 2020 | schizophrenia | Neurocrine Biosciences | Completed | Missed primary |
| Phase 2 | NCT03382639 | Jan 2018 → Dec 2020 | schizophrenia | Neurocrine Biosciences | Completed | Missed primary |
| Phase 2 | NCT03214588 | Nov 2017 → Dec 2018 | Friedreich ataxia | Neurocrine Biosciences | Completed | Missed primary |
Evidence & citations 7 cited values
Every value below carries the sentence it was read from. 13 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Luvadaxistat | ClinicalTrials.gov intervention name — accepted as the source's own label NCT05182476 ↗ |
| Known as | NBI-1065844 | “Luvadaxistat (TAK-831/NBI-1065844) is an investigational d-amino acid oxidase (DAAO) inhibitor that increases d-serine levels at NMDAR coagonist sites.” PMID 38943928 ↗ Jun 2024 |
| Known as | TAK-831 | “Luvadaxistat (TAK-831/NBI-1065844) is an investigational d-amino acid oxidase (DAAO) inhibitor that increases d-serine levels at NMDAR coagonist sites.” PMID 38943928 ↗ Jun 2024 |
| Action | Inhibit | “TAK-831 is a highly selective and potent inhibitor of DAO” NCT02716987 ↗ |
| Modality | Small molecule | — CHEMBL2338801 ↗ |
| Route | Oral | “TAK-831 oral suspension.” NCT02566759 ↗ |
| Target | DAO | “TAK-831 is a highly selective and potent inhibitor of DAO” NCT02716987 ↗ |