jRCTs031240259招募中不适用
BENralizumab dosing interval Extension to 12 weeks in severe asthma patients; a multicenter phase II study to evaluate the safety and efFIcacy (BENEFIT trial)
未提供0 个研究点目标入组 30 人开始时间: 2024年11月22日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 主要终点
- Annual asthma exacerbation rate
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Single Arm Study
- 干预模型
- Single Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Open(masking Not Used)
入排标准
- 年龄范围
- 18age old over 至 No limit(—)
- 性别
- All
入选标准
- •(1) Diagnosis of bronchial asthma and continuous treatment with benralizumab for at least 1 year prior to study initiation.
- •(2) No more than 1 asthma exacerbation in the past year.
- •(3) No asthma exacerbations within the past 3 months.
- •(4) No increase in controller medication dosage due to symptom worsening in the past year (dose reductions or discontinuations of controllers are permitted).
- •(5) Age 18 years or older.
- •(6) Provision of written informed consent to participate in this study.
排除标准
- •(1) Current or prior use of other biologic agents for asthma within the past 1 year.
- •(2) History of severe asthma exacerbation requiring mechanical ventilation.
- •(3) Pregnant or lactating women, those with a possibility of being pregnant, or those who desire to become pregnant during the treatment period.
- •(4) Patients with a potential for parasitic infection.
- •(5) Any other patients deemed ineligible for the study based on the investigator's clinical judgment.
结局指标
主要结局
Annual asthma exacerbation rate
时间窗: Annual
Total number of exacerbations × 365.25 / total treatment period follow-up duration in days
次要结局
- Asthma Control Questionnaire (ACQ) score
研究者
相似试验
招募中
1 期
Dose-ranging Study: Safety, Tolerability and Immunogenicity of INO-4500 in Healthy Volunteers in GhanaLassa FeverPACTR201910864382850Inovio Pharmaceuticals220
尚未招募
不适用
An open-label, phase Ib, dose-escalation trial on the safety, tolerability, pharmacokinetics, immunogenicity, biological effects and antitumor activity of EMD 521873 in combination with local irradiation (20 Gy) of primary tumors or metastases in subjects with non-small cell lung cancer stage IIIb with malignant pleural effusion or stage IV with disease control (partial response or stable disease) after application of 4 cycles of platinum-based, first-line chemotherapy.non-small cell lung carcinoma10038666Lung cancerNL-OMON34011Merck KGaA24
已完成
不适用
An open-label, dose escalating Phase Ib study for the assessment of safety, tolerability, pharmacokinetics, and pharmacodynamics of multiple intravenous doses of GLPG0187 in subjects with solid tumors.solid neoplasmsolid tumors10027655NL-OMON36388Galapagos SAS19
尚未招募
1 期
Study of NM8074 in Adult C3 Glomerulopathy PatientsC3 GlomerulopathyNCT05647811NovelMed Therapeutics18
招募中
1 期
Open-label, dose-escalation trial to evaluate the safety and pharmacokinetics of GEN1046 in Japanese subjects with advanced solid malignanciesSolid tumorJPRN-jRCT2031210112jRCT Inquiry Receipt Center39
