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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)

2026年11月4日 更新者:Bayer

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

地位

主动,不招人

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

观察性的

注册 (估计的)

1200

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Many Locations、印度
        • Many locations

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

取样方法

非概率样本

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

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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
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
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
2022年至2024年回顾性数据分析
Finerenone 起始日期
大体时间:2022年至2024年回顾性数据分析
2022年至2024年回顾性数据分析
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
2022年至2024年回顾性数据分析
Finerenone 停药日期
大体时间:2022年至2024年回顾性数据分析
2022年至2024年回顾性数据分析
停用 Finerenone 的原因
大体时间:2022年至2024年回顾性数据分析
2022年至2024年回顾性数据分析
Finerenone治疗剂量
大体时间:2022年至2024年回顾性数据分析
2022年至2024年回顾性数据分析
Finerenone 治疗的频率
大体时间:2022年至2024年回顾性数据分析
2022年至2024年回顾性数据分析
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
2022年至2024年回顾性数据分析
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
2022年至2024年回顾性数据分析
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
2022年至2024年回顾性数据分析
Actions taken after finerenone introduction
大体时间:Retrospective data analysis from 2022 to 2024

Actions include continue treatment, addition of second therapy like SGLT2is, potassium binders, discontinue treatment

Retrospective data analysis from 2022 to 2024
Actions taken after stop finerenone prescription
大体时间:Retrospective data analysis from 2022 to 2024

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

次要结果测量

结果测量
措施说明
大体时间
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
2022年8月至2024年4月回顾性数据分析
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
2022年至2024年回顾性数据分析
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
2022年8月至2024年4月回顾性数据分析
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
2022年8月至2024年4月回顾性数据分析
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
2022年8月至2024年4月回顾性数据分析
UACR (mg/g) before and after initiating finerenone
大体时间:Retrospective data analysis from Aug 2022 to Apr 2024

UACR: Urine Albumin to Creatinine Ratio

Retrospective data analysis from Aug 2022 to Apr 2024
eGFR before and after initiating finerenone
大体时间:Retrospective data analysis from Aug 2022 to Apr 2024

eGFR: Estimated glomerular filtration rate

Retrospective data analysis from Aug 2022 to Apr 2024

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年9月22日

初级完成 (估计的)

2026年11月30日

研究完成 (估计的)

2026年11月30日

研究注册日期

首次提交

2025年1月2日

首先提交符合 QC 标准的

2025年1月2日

首次发布 (实际的)

2025年1月8日

研究记录更新

最后更新发布 (实际的)

2026年11月5日

上次提交的符合 QC 标准的更新

2026年11月4日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

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.

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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