FINErenone druG Utilization Study and Assessment of Temporal Changes Following Availability of Different Treatment Options in Patients With Chronic Kidney Disease and Type 2 Diabetes
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Bayer
- 入组人数
- 50,000
- 试验地点
- 2
- 主要终点
- Descriptive summary of baseline patient characteristics
研究概览
简要总结
This is an observational study in which data from people with chronic kidney disease (CKD) and type 2 diabetes (T2D) who have already started or will start CKD or T2D treatment are collected and studied. In observational studies, only observations are made without specified advice or interventions.
People receiving the following CKD or T2D treatments as recommended by their doctors will be included:
- Sodium-glucose cotransporter 2 inhibitors (SGLT2i),
- Glucagon-like peptide-1 receptor agonists (GLP-1 RA),
- Steroidal mineralocorticoid receptor antagonists (sMRA),
- Finerenone, a non-steroidal mineralocorticoid receptor antagonist (nsMRA)
- Other nsMRA (only in Japan)
Kidneys filter extra water and waste from the blood and make urine. CKD is a long-term, progressive decrease in the kidneys' ability to properly filter blood. In people with T2D, the body does not make enough of a hormone called insulin or does not use insulin well enough, resulting in high blood sugar levels that can cause damage to the kidneys. As a result, CKD can occur as a complication of T2D.
The new drug, finerenone, works by blocking certain proteins, called mineralocorticoid receptors. An increased stimulation of these proteins is thought to damage the kidneys. By lowering their stimulation, finerenone reduces the risk of progressive worsening of the kidney disease.
Finerenone is available and approved in several countries for doctors to prescribe to people with CKD and T2D.
The main purpose of the study is to collect and describe characteristics of participants in each treatment group who have started or will start treatment before and after finerenone became available.
To do this, the researchers will collect data on:
- Patient characteristics (e.g., age sex) of the participants
- Clinical characteristics (e.g., history of CKD and T2D, heart and liver health, other health problems) of the participants
- Treatments for T2D and CKD
- Other medications used
Data will be grouped by type of treatment that is initiated (e.g., SGLT2i, a GLP-1 RA, a sMRA, finerenone, or other nsMRA). Two time periods will be compared. Study period I is the time until finerenone became available in the respective country, starting from 2012 (2014 for Japan). Study period II will begin when finerenone becomes available in the respective country and will end at the end of the study (planned in September 2024).
Researchers will also collect data on treatment patterns and changes for each type of treatment in both time periods.
Health care data will be collected from various sources in five countries (e.g., Denmark, the Netherlands, Spain, Japan, and the US).
The patients will receive their treatment as prescribed by their doctors during routine practice according to the approved product information.
Each patient will be in the study from first use (in Study period I and II) of one of the listed drug classes until:
- End of study
- The data are somehow no longer available
- The patient leaves or has to leave the study
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Active registration or continuous enrolment for at least 12 months in 1 of the selected data sources before the index date
- •No recorded prescription or dispensing of any medication in the class during the 12 months before the index date
- •Age 18 years or older as of the index date
- •Diagnosis of T2D on or before the index date
- •Diagnosis of CKD on or before the index date
排除标准
- •Type 1 diabetes identified by appropriate algorithms in each participating data source
- •Kidney cancer on or before the index date
- •Kidney failure
- •- Maintenance dialysis on or before the index date
- •Kidney transplantation on or before the index date
研究组 & 干预措施
Patients with CKD+T2D in Study period I
In the pre-finerenone approval period (Study period I), 4 new-user cohorts to be identified, based on the first use of any drug in these classes: SGLT2i, GLP-1 RA, sMRA, or nsMRA.
干预措施: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) (Drug)
Patients with CKD+T2D in Study period I
In the pre-finerenone approval period (Study period I), 4 new-user cohorts to be identified, based on the first use of any drug in these classes: SGLT2i, GLP-1 RA, sMRA, or nsMRA.
干预措施: Glucagon-like peptide-1 receptor agonists (GLP 1 RA) (Drug)
Patients with CKD+T2D in Study period I
In the pre-finerenone approval period (Study period I), 4 new-user cohorts to be identified, based on the first use of any drug in these classes: SGLT2i, GLP-1 RA, sMRA, or nsMRA.
干预措施: Steroidal mineral corticoid receptor antagonists (sMRA) (Drug)
Patients with CKD+T2D in Study period I
In the pre-finerenone approval period (Study period I), 4 new-user cohorts to be identified, based on the first use of any drug in these classes: SGLT2i, GLP-1 RA, sMRA, or nsMRA.
干预措施: Non-steroidal mineral corticoid receptor antagonists (nsMRA) (Drug)
Patients with CKD+T2D in Study period II
In the post-finerenone study period (study period II), 3 new-user cohorts will be identified: SGLT2i, GLP-1 RA, and finerenone.
干预措施: Finerenone (Kerendia, BAY 948862) (Drug)
Patients with CKD+T2D in Study period II
In the post-finerenone study period (study period II), 3 new-user cohorts will be identified: SGLT2i, GLP-1 RA, and finerenone.
干预措施: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) (Drug)
Patients with CKD+T2D in Study period II
In the post-finerenone study period (study period II), 3 new-user cohorts will be identified: SGLT2i, GLP-1 RA, and finerenone.
干预措施: Glucagon-like peptide-1 receptor agonists (GLP 1 RA) (Drug)
结局指标
主要结局
Descriptive summary of baseline patient characteristics
时间窗: Baseline study periods I and II
Demographic (Age, Sex, Race and Socioeconomic status ) and clinical characteristics (markers of severity of T2D and of kidney dysfunction ) data will be collected.
Descriptive summary of patient comorbidities
时间窗: Baseline study periods I and II
History of coronary heart disease, cerebrovascular disease, peripheral vascular disease, hypertension, hypercholesterolemia, Congestive heart failure, Severe liver disease, Other comorbidities measured by the Charlson or similar comorbidity indices. Lifestyle factors as Body mass index (BMI) or evidence of obesity, Smoking status, and alcohol abuse and alcohol abuse-related conditions, as available in each data source.
Descriptive summary of patient comedications
时间窗: Baseline study periods I and II
Medications for T2D, CKD and other relevant medications.
次要结局
- Descriptive summary of changes over time in treatments in the new-user cohorts(From Day 1 until Censor Day (at the earliest of death, disenrolment, exclusion criteria during follow-up, or end of the study period) [up to 114 months for study period I and up to 39 months for study period II].)
- Descriptive summary of temporal changes in the baseline characteristics of medication-specific cohorts(Baseline up to 114 months for study period I and up to 39 months for study period II)