Condition: Hemophilia A · Sponsor: Hoffmann-La Roche
The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics and pharmacodynamics of NXT007 prophylaxis compared with Factor VIII (FVIII) prophylaxis in participants with severe or moderate congenital hemophilia A without inhibitors. The study will include people aged ≥12 years old with severe or moderate congenital hemophilia A without inhibitors on previous FVIII prophylaxis treatment.
This description comes directly from the study's public registry record.
Reference Study ID Number: WO45886 https://forpatients.roche.com/ No attachments to email below. · 888-662-6728 (U.S. Only) · global-roche-genentech-trials@gene.com
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| Nara Medical University Hospital | Kashihara-shi, Nara, Japan | Recruiting |
| Tokyo Medical University Hospital | Shinjuku-Ku, Tokyo, Japan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07416526