Research Study to Look at How Well the Drug Concizumab Works in Your Body if You Have Haemophilia Without Inhibitors
3期
进行中(已停止招募)
NCT04082429
| 适应症 | Haemophilia A Without Inhibitors, Haemophilia B Without Inhibitors |
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| 分期 | 3期 |
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| 申办方 | Novo Nordisk A/S |
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| 状态 | 进行中(已停止招募) |
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| 受试者人数 | 156 人 |
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| 干预(药物) | Concizumab |
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| 开始日期 | 2019年11月13日 |
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| 完成日期 | 2022年7月12日 |
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| 结果公布日 | 2025年10月31日 |
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摘要
This study will test how well a new medicine called concizumab works in the body of people with haemophilia A or B without inhibitors. The purpose is to show that concizumab can prevent bleeds in the body and is safe to use. Participants who usually only take medicine to treat bleeds (on-demand) will be placed in one of two groups. In one group participants will get study medicine from the start of the study. In the other group participants will continue with their normal medicine and get study medicine after 6 months. Which treatment the participant gets is decided by chance. Participants who usually take medicine to prevent bleeds (prophylaxis treatment) or who are already being treated with concizumab (study medicine) will receive the study medicine from the start of the study. Participants will have to inject themselves with the study medicine 1 time every day under the skin. This can be done at home. The study doctor will hand out the medicine in the form of a pen-injector. The pen-injector will contain the study medicine. The study will last for up to 8 years. The length of time the participant will be in the study depends on when they agreed to take part and when the medicin
Haemophilia A Participants Without Inhibitors: Rate of Treated Spontaneous and Traumatic Bleeding Episodes
On demand (arm 1): From week 0 up until start of concizumab treatment (week 24); Concizumab (arm 2): From week 0 up until the confirmatory analyses cut-off · Events per year
| Arm 1: Previous On Demand (OnD) Treatment: No Prophylaxis (PPX) - Participants With HA | 19.6 Events per year |
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| Arm 2: Previous OnD Treatment: Concizumab PPX - Participants With HA | 2.9 Events per year |
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| p-value | <0.001 |
| ABR ratio | 0.14 (95% CI 0.07–0.29) |
Haemophilia B Participants Without Inhibitors: Rate of Treated Spontaneous and Traumatic Bleeding Episodes
On demand (arm 1): From week 0 up until start of concizumab treatment (week 24); Concizumab (arm 2): From week 0 up until the confirmatory analyses cut-off · Events per year
| Arm 1: Previous OnD Treatment: No PPX - Participants With HB | 14.9 Events per year |
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| Arm 2: Previous OnD Treatment: Concizumab PPX - Participants With HB | 1.6 Events per year |
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| p-value | <0.001 |
| ABR ratio | 0.21 (95% CI 0.10–0.45) |
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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。