2022-502727-21-00招募中3 期
A prospective, post-authorisation long-term follow up trial of patients previously treated with imlifidase prior to kidney transplantation, including a non-comparative concurrent reference cohort
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 126
- 试验地点
- 16
- 主要终点
- Graft failure-free survival (%) up to 5 years after imlifidase enabled transplantation(imlifidase cohort only)
研究概览
简要总结
To evaluate long-term graft failure-free survival in highly sensitised kidney transplant patients after imlifidase administration in trial 20-MedIdeS-19 (PAES) (imlifidase cohort only)
入排标准
- 年龄范围
- 18 years 至 65+ years(18-64 Years, 65+ Years)
- 接受健康志愿者
- 是
入选标准
- •Signed Informed Consent obtained before any trial-related procedures.
- •Willingness and ability to comply with the protocol.
- •Previously transplanted in the clinical trial 20-HmedIdeS-19 (PAES).
排除标准
- •Inability by the judgment of the investigator to participate in the trial for other reasons.
结局指标
主要结局
Graft failure-free survival (%) up to 5 years after imlifidase enabled transplantation(imlifidase cohort only)
Graft failure-free survival (%) up to 5 years after imlifidase enabled transplantation(imlifidase cohort only)
次要结局
- Graft failure-free survival (%) up to 5 years after transplantation (non-comparativeconcurrent reference cohort only)
- Graft failure-free survival (%) up to 2 and 3 years after transplantation
- Renal function as evaluated by estimated Glomerular Filtration Rate (eGFR) andserum/plasma creatinine levels
- Patient survival (%) after transplantation
- Graft survival (%) after transplantation
- HLA/DSA levels (imlifidase cohort only)
- ADA levels (imlifidase cohort only)
- Proportion of patients (%) with biopsy- and serology (DSA)-confirmed AMRs
- Proportion of patients (%) with biopsy confirmed CMRs.
- Treatment of graft rejection episodes
- Adverse events (AEs)/serious adverse events (SAEs) suspected to be related toimlifidase treatment (imlifidase cohort only)
- Ongoing immunosuppressive medication
- Comorbidity
- Change in patient reported life participation, as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Social Health domain “Ability to participate in social roles & activities, PROMIS-SF-8a”, from baseline to 5 years after transplantation
研究者
Clinical contact information
Scientific
Hansa Biopharma AB
研究点 (16)
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