Anifrolumab Asian PhIII Efficacy Study for Systemic Lupus Erythematosus (SLE)
| Заболевание | Active Systemic Lupus Erythematosus |
|---|---|
| Фаза | Фаза 3 |
| Спонсор | AstraZeneca |
| Статус | Завершено |
| Участники | 277 участн. |
| Вмешательство | Anifrolumab |
| Дата начала | 13.09.2021 |
| Дата завершения | 7.04.2025 |
| Публикация результатов | 20.05.2026 |
Кратко
The purpose of this study is to evaluate the efficacy and safety of an intravenous treatment regimen of anifrolumab versus placebo in Asian participants with active systemic lupus erythematosus (SLE).
Difference in Proportion of Participants Who Are Responders Between Anifrolumab and Placebo
| Anifrolumab 300mg | 84 Participants |
|---|---|
| Placebo | 46 Participants |
| p-value | >0.999 |
|---|---|
| Rate difference (%) | 28.4 |
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