- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT06763146
En observationsundersøgelse for at lære mere om, hvor sikkert Finerenone er, og hvor godt det virker hos indiske mennesker med kronisk nyresygdom og type 2-diabetes i rutinemæssig medicinsk praksis (IN-REALITY)
Erfaring fra den virkelige verden med finerenonbehandling hos patienter fra Indien med kronisk nyresygdom og type 2-diabetes - retrospektiv dataanalyse
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.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiesteder
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-
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Many Locations, Indien
- Many locations
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-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Patients with a diagnosis of CKD associated with T2D who are initiated on finerenone under routine clinical management.
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Observationsmodeller: COHORT
- Tidsperspektiver: RETROSPECTIVE
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
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. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Beskrivende resumé af ordinerende læges speciale
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
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Retrospektiv dataanalyse fra 2022 til 2024
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Dato for finerenoninitiering
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
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Retrospektiv dataanalyse fra 2022 til 2024
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|
|
Hvis patienten fik finerenon på tidspunktet for hvert opfølgningsbesøg (Ja/Nej)
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
|
Retrospektiv dataanalyse fra 2022 til 2024
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Dato for seponering af finerenon
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
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Retrospektiv dataanalyse fra 2022 til 2024
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Årsag til seponering af finerenon
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
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Retrospektiv dataanalyse fra 2022 til 2024
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Dosis af finerenonbehandling
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
|
Retrospektiv dataanalyse fra 2022 til 2024
|
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Hyppighed af finerenonbehandling
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
|
Retrospektiv dataanalyse fra 2022 til 2024
|
|
|
Antallet af patienter, der startede finerenon med en dosis på 10 mg og 20 mg
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
|
Retrospektiv dataanalyse fra 2022 til 2024
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Andelen af patienter, der startede finerenon med en dosis på 10 mg og er optitreret til en dosis på 20 mg
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
|
Retrospektiv dataanalyse fra 2022 til 2024
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Andelen af patienter, der startede finerenon med en dosis på 20 mg og er nedtitreret til en dosis på 10 mg
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
|
Retrospektiv dataanalyse fra 2022 til 2024
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Actions taken after finerenone introduction
Tidsramme: 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
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|
Actions taken after stop finerenone prescription
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Serumkalium (mmol/L) før og efter påbegyndelse af finerenon
Tidsramme: Retrospektiv dataanalyse fra august 2022 til april 2024
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Retrospektiv dataanalyse fra august 2022 til april 2024
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Ændring i UACR efter påbegyndelse af finerenon vs. måned 1, måned 4 og afslutning af undersøgelsen
Tidsramme: Retrospektiv dataanalyse fra 2022 til 2024
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Retrospektiv dataanalyse fra 2022 til 2024
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Ændring i serumkalium efter påbegyndelse af finerenon vs. måned 1, måned 4 og afslutning af undersøgelsen
Tidsramme: Retrospektiv dataanalyse fra august 2022 til april 2024
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Retrospektiv dataanalyse fra august 2022 til april 2024
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Ændring i serumkreatinin/eGFR efter påbegyndelse af finerenon versus måned 1, måned 4 og afslutning af undersøgelsen
Tidsramme: Retrospektiv dataanalyse fra august 2022 til april 2024
|
Retrospektiv dataanalyse fra august 2022 til april 2024
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Hyppighed af hændelser som hospitalsindlæggelse og dialyse på grund af hyperkaliæmi
Tidsramme: Retrospektiv dataanalyse fra august 2022 til april 2024
|
Retrospektiv dataanalyse fra august 2022 til april 2024
|
|
|
UACR (mg/g) before and after initiating finerenone
Tidsramme: 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
Tidsramme: Retrospective data analysis from Aug 2022 to Apr 2024
|
eGFR: Estimated glomerular filtration rate |
Retrospective data analysis from Aug 2022 to Apr 2024
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Urogenitale sygdomme
- Sygdomme i det endokrine system
- Patologiske processer
- Mandlige urogenitale sygdomme
- Nyresygdomme
- Urologiske sygdomme
- Urogenitale sygdomme hos kvinder
- Kvinders urogenitale sygdomme og graviditetskomplikationer
- Kronisk sygdom
- Sygdomsegenskaber
- Metaboliske sygdomme
- Glukosemetabolismeforstyrrelser
- Diabetes mellitus
- Nyreinsufficiens
- Patologiske tilstande, tegn og symptomer
- Ernæringsmæssige og metaboliske sygdomme
- Diabetes mellitus, type 2
- Nyreinsufficiens, kronisk
- finereonon
Andre undersøgelses-id-numre
- 22549
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
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.
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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