一项观察性研究旨在进一步了解 Finerenone 的安全性以及其在印度慢性肾病和 2 型糖尿病患者日常医疗实践中的疗效 (IN-REALITY)
印度慢性肾病和 2 型糖尿病患者的 Finerenone 治疗真实经验——回顾性数据分析
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.
Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.
研究概览
详细说明
This is an observational study in which data already collected from people with chronic kidney disease (CKD) and Type 2 diabetes mellitus (T2D) are studied.
T2D is a condition in which glucose levels rise in the blood. It is one of the common causes of CKD and can lead to kidney failure. CKD is a long-term condition in which the kidneys' ability to work properly gradually decreases over time.
The study drug, finerenone, is already approved for doctors to prescribe to people with CKD and T2D. It blocks the activity of a protein involved in worsening kidney function.
People with CKD and T2D are already receiving treatment with finerenone based on the results of previous studies. These studies, however, did not include Indian participants.
To better understand the impact of finerenone on CKD and T2D, more knowledge is needed about how well it works in the Indian population.
The main purpose of the study is to learn more about how well finerenone works and how safe it is in Indian people with CKD and T2D. To do this, researchers will check:
- participants' characteristics including age, sex, height and weight, and signs and symptoms of the disease
- other conditions the participants may have along with CKD and T2D, additional medicines they have taken with finerenone, and different treatment patterns in Indian participants.
The different treatment pattern for finerenone includes:
- specialty of the doctor who prescribed finerenone
- the date of starting finerenone
- whether participants were still taking finerenone at each follow-up visit
- the date and reason for stopping finerenone early
- the dose of finerenone the participants took and how often they took it
- changes in the dosage either with a low dose or high dose compared with the previous firenone dose
- after starting finerenone treatment: reseachers may ask to continue treatment with finerenone, or may suggest adding other treatments like SGLT2 inhibitors or potassium binders, or stop finerenone treatment
- after stopping finerenone treatment: researchers may start other treatments, like SGLT2 inhibitors, RAAS inhibitors, or potassium binders or other therapy
Researchers will only look at the medical records from participants in India. Data collected will be from August 2022 to April 2024.
Researchers will track participants' data in India and will follow them until the end of the study period till Nov 2024, last visit date of the participant, the participant discontinues treatment with finerenone, death, kidney failure, or cancer of the kidney.
In this study, only available data from routine care in India are collected. No visits or tests are required as part of this study.
研究类型
注册 (估计的)
联系人和位置
学习地点
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Many Locations、印度
- Many locations
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
Patients with a diagnosis of CKD associated with T2D who are initiated on finerenone under routine clinical management.
描述
Inclusion Criteria:
- Patients from India (Indian ethnicity) diagnosed with CKD and T2D prior to initiating finerenone (per the standard diagnostic criteria) and initiated on finerenone per approved label.
- Patient was prescribed finerenone for the first time (drug naïve) for the management of CKD and T2D between 1st August 2022 and 30th April 2024.
- Age 18 years or older at the time of finerenone initiation.
Exclusion Criteria:
- eGFR <25 mL/min/1.73 m^2
- Serum potassium >5.0 mmol/L
- Type 1 diabetes is recorded in the patient record
- Contraindications according to the local marketing authorization - Patient data will be excluded if below information is identified in the patient record at any point from index date to the end of observation period:
- - Pregnancy.
- - Lactation.
- - Patient taking concomitant medications that are strong CYP3A4 inhibitors (e.g., itraconazole, ketoconazole, ritonavir, nelfinavir, cobicistat, clarithromycin, telithromycin and nefazodone).
- - Addison's disease.
- Patient was a part of an interventional clinical study between 1st August 2022 and 30th Nov 2024.
学习计划
研究是如何设计的?
设计细节
- 观测模型:COHORT
- 时间观点:RETROSPECTIVE
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
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Finerenone (Kerendia, BAY948862)
Patients with CKD and T2D from India who initiate on finerenone per approved label. |
Retrospective cohort analysis using the investigator or a delegate at the study site collects secondary/historic data of finerenone usage (patient demographic and clinical characteristics, diagnosis-related, treatment-related, and laboratory data) from clinic specific medical records. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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处方医师专业描述性摘要
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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Finerenone 起始日期
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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患者在每次随访时是否正在接受 Finerenone(是/否)
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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Finerenone 停药日期
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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停用 Finerenone 的原因
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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Finerenone治疗剂量
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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Finerenone 治疗的频率
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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开始使用 10 mg 剂量和 20 mg 剂量的 Finerenone 的患者人数
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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开始使用 10 mg 剂量的 Finerenone 并逐渐调整至 20 mg 剂量的患者比例
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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开始使用 20 毫克剂量的 Finerenone 并下调至 10 毫克剂量的患者比例
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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Actions taken after finerenone introduction
大体时间:Retrospective data analysis from 2022 to 2024
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Actions include continue treatment, addition of second therapy like SGLT2is, potassium binders, discontinue treatment |
Retrospective data analysis from 2022 to 2024
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Actions taken after stop finerenone prescription
大体时间:Retrospective data analysis from 2022 to 2024
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Actions include initiate alternate therapy like Sodium-glucose transport protein-2 inhibitor (SGLT2is), RAASis or potassium binders, other |
Retrospective data analysis from 2022 to 2024
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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开始使用finerenone前后的血清钾(mmol/L)
大体时间:2022年8月至2024年4月回顾性数据分析
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2022年8月至2024年4月回顾性数据分析
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开始使用 Finerenone 后 UACR 与第 1 个月、第 4 个月和研究结束时的变化
大体时间:2022年至2024年回顾性数据分析
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2022年至2024年回顾性数据分析
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开始使用 Finerenone 后与第 1 个月、第 4 个月和研究结束时血清钾的变化
大体时间:2022年8月至2024年4月回顾性数据分析
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2022年8月至2024年4月回顾性数据分析
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开始使用 Finerenone 后与第 1 个月、第 4 个月和研究结束时血清肌酐/eGFR 的变化
大体时间:2022年8月至2024年4月回顾性数据分析
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2022年8月至2024年4月回顾性数据分析
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由于高钾血症而住院和透析等事件的频率
大体时间:2022年8月至2024年4月回顾性数据分析
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2022年8月至2024年4月回顾性数据分析
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UACR (mg/g) before and after initiating finerenone
大体时间:Retrospective data analysis from Aug 2022 to Apr 2024
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UACR: Urine Albumin to Creatinine Ratio |
Retrospective data analysis from Aug 2022 to Apr 2024
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eGFR before and after initiating finerenone
大体时间:Retrospective data analysis from Aug 2022 to Apr 2024
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eGFR: Estimated glomerular filtration rate |
Retrospective data analysis from Aug 2022 to Apr 2024
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- 22549
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.
Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.
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研究美国 FDA 监管的设备产品
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