Condition: Paroxysmal Nocturnal Hemoglobinuria · Sponsor: AstraZeneca
As part of a post-approval commitment, the Korean health authority requests a study to characterize safety and effectiveness in patients who are treated with Danicopan as an add-on to ravulizumab or eculizumab in normal clinical practice settings. This study is designed to assess the known safety profile or identify previously unsuspected adverse reactions and to evaluate the effectiveness of Danicopan under conditions of routine daily medical practice in Korea.
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 | Busan, South Korea | Recruiting |
| Research Site | Hwasun-gun, South Korea | Recruiting |
| Research Site | Seoul, South Korea | Recruiting |
| Research Site | Seoul, South Korea | Active Not Recruiting |
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Source record: clinicaltrials.gov/study/NCT07457151