DRKS00028582已完成不适用
Prophylaxis Impact on Quality of Life Impariment of HAE Patients with Lower Annual Base Attack Rates - PIQHAR
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Takeda GmbH
- 入组人数
- 22
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 12 Years 至 one（—）
- 性别
- All
入选标准
- •Confirmed diagnosis of HAE Type 1/2.
- •- Voluntarily provision of written, signed, and dated (personally or via a legally authorized representative) informed consent to participate in the study.
- •- Initiation of treatment with lanadelumab in accordance with current product labelling.
- •- Documented history of = 24 attacks in the year prior to enrollment AND baseline AE-QoL Score of = 30 points.
- •- 12 years or older.
排除标准
- •- Inability to provide written, signed, and dated informed consent.
- •- Documented history of > 24 confirmed HAE attacks/year in the year prior to study enrollment OR baseline AE-QoL Score of < 30 points.
- •- Participation in the study ruled out by the treating physician/investigator.
- •- Pregnant or breastfeeding.
- •- Current or planned participation in interventional studies.
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