Condition: Von Willebrand Disease (VWD) · Sponsor: Takeda
The main aim of this study is to find out if VONVENDI is safe for adult Chinese participants with VWD. The study will also check how well VONVENDI helps control bleeding with or without product ADVATE in the participants who may need elective surgery or dental procedures. In addition, the study will also examine how VONVENDI is processed by the body (known as pharmacokinetic \[PK\]) and how the drug helps the body respond or improve a condition (pharmacodynamic \[PD\]). Participants will receive an initial dose of VONVENDI of 40 to 80 international units per kilogram (IU/kg) of body weight. If a participant's baseline factor VIII (FVIII) level is not high enough to help stop bleeding, VONVENDI will be given along with 30 to 45 IU/kg of ADVATE rFVIII. Participants will be in the study for approximately 14 months. During the study, participants will be followed up at clinics or over telephone calls.
This description comes directly from the study's public registry record.
Takeda Contact · +1-877-825-3327 · medinfoUS@takeda.com
Always discuss trial participation with your own doctor first.
| Peking Union Medical College Hospital | Beijing, China | Recruiting |
| Nanfang Hospital Southern Medical University | Guangzhou, China | Recruiting |
| Jinan Central Hospital | Jihan, China | Recruiting |
| Ruijin Hospital Shanghai Jiaotong University School of Medicine | Shanghai, China | Recruiting |
| The First Affiliated Hospital of Soochow University | Suzhou, China | Recruiting |
| Institute of Hematology and Blood Diseases Hospital Chinese Academy of Medical Sciences | Tianjin, China | Recruiting |
| Tongji Hospital Tongji Medical College Huazhong University of Science and Technology | Wuhan, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07129343