Condition: Life Threatening Bleeding · Factor Xa Inhibitor · Sponsor: AstraZeneca
This survey will be conducted to investigate the status of occurrence of the safety specifications set for "Safety specification" in patients who received Ondexxya Intravenous Injection 200 mg. In addition, this survey will be implemented to understand the followings by collecting safety and effectiveness information under actual use conditions.
This description comes directly from the study's public registry record.
AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
Always discuss trial participation with your own doctor first.
| Research Site | Aichi, Japan | Withdrawn |
| Research Site | Aichi, Japan | Recruiting |
| Research Site | Akita, Japan | Withdrawn |
| Research Site | Aomori, Japan | Withdrawn |
| Research Site | Chiba, Japan | Withdrawn |
| Research Site | Chiba, Japan | Active Not Recruiting |
| Research Site | Ehime, Japan | Active Not Recruiting |
| Research Site | Ehime, Japan | Withdrawn |
| Research Site | Fukui, Japan | Withdrawn |
| Research Site | Fukui, Japan | Active Not Recruiting |
| Research Site | Fukuoka, Japan | Withdrawn |
| Research Site | Fukuoka, Japan | Active Not Recruiting |
+ 49 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT05454787