JPRN-jRCT2051210047进行中(未招募)3 期
Study of Efficacy and Safety of Twice Daily Oral Iptacopan (LNP023) in Adult PNH Patients Who Are Naive to Complement Inhibitor Therapy - APPOINT-PNH
Suzuki Kazuyuki0 个研究点目标入组 40 人开始时间: 2021年7月9日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 18age old 至 ot applicable(—)
- 性别
- All
入选标准
- •Male and female participants >= 18 years of age with a diagnosis of PNH confirmed by high-sensitivity flow cytometry with clone size >= 10%
- •- Mean hemoglobin level <10 g/dL
- •- LDH > 1.5 x Upper Limit of Normal (ULN)
- •- Vaccination against Neisseria meningitidis infection is required prior to the start of study treatment
- •- If not received previously, vaccination against Streptococcus pneumoniae and Haemophilus influenzae infections should be given
排除标准
- •- Prior treatment with a complement inhibitor, including anti-C5 antibody
- •- Known or suspected hereditary complement deficiency
- •- History of hematopoietic stem cell transplantation
- •- Patients with laboratory evidence of bone marrow failure (reticulocytes <100E9/L; platelets <30E9/L; neutrophils <0.5E9/L).
- •- Active systemic bacterial, viral (incl. COVID-19)or fungal infection within 14 days prior to study drug administration.
- •- History of recurrent invasive infections caused by encapsulated organisms, e.g. meningococcus or pneumococcus.
- •- Major concurrent comorbidities including but not limited to severe kidney disease (e.g., dialysis), advanced cardiac disease (e.g., NYHA class IV heart failure), severe pulmonary disease (e.g., severe pulmonary hypertension (WHO class IV)), or hepatic disease (e.g., active hepatitis) that in the opinion of the investigator precludes participant's participation in the study.
研究者
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