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Study · Not a test of the peptide alone · 2025

7 results

Real-World Effectiveness of Finerenone Added to SGLT2 Inhibitor and GLP-1 Receptor Agonist Therapy in Individuals with Type 2 Diabetes and Chronic Kidney Disease.

Nakhleh A, Khazim K, Shehadeh N

Journal of clinical medicine19 Nov 2025Cited by 2 (Europe PMC)

Summary

Background/Objectives: Recent randomized controlled trial evidence in adults with type 2 diabetes (T2D) and chronic kidney disease (CKD) indicates that adding finerenone to empagliflozin provides additive clinical benefit. A prespecified analysis demonstrates that this benefit is consistent irrespective of prior glucagon-like peptide-1 receptor agonist (GLP-1 RA) use. We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting. Methods: We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel. Included individuals initiated finerenone between 1 August 2023, and 31 January 2025, and met the following criteria: estimated glomerular filtration rate (eGFR) of 25-60 mL/min/1.73 m2; urinary albumin-to-creatinine ratio (UACR) > 300 mg/g; and a history of ≥12 weeks of SGLT2i (empagliflozin or dapagliflozin) and GLP-1 RA (liraglutide, dulaglutide, or semaglutide) use prior to finerenone initiation. Outcomes were assessed at the last measurement taken within 26 ± 10 weeks of finerenone initiation. The primary outcome was adjusted percent change in log-transformed UACR from baseline to follow-up. Secondary outcomes were adjusted mean changes in eGFR and serum potassium. We used multiple linear regression models. Prespecified subgroup analyses examined the UACR change by age, sex, body mass index (BMI), baseline eGFR, and baseline UACR. Results: Fifty-one individuals were included in the study, with a mean age of 66.0 ± 9.5 years and a mean BMI 30.9 ± 5.2 kg/m2. The median eGFR was 45 mL/min/1.73 m2 (IQR 36-52), and the median UACR was 1001 mg/g (IQR 515-1599). 94% were receiving a renin-angiotensin system inhibitor. Finerenone was initiated at 10 mg/day and titrated to 20 mg/day in eight individuals. Over a median follow-up of 27 weeks, the adjusted percent change in UACR was -51.3% (p < 0.001), consistent across prespecified subgroups. The adjusted mean eGFR change was -3.92 mL/min/1.73 m2 (p < 0.001). Serum potassium increased by +0.34 mmol/L (p < 0.001). Conclusions: In adults with T2D and albuminuric CKD already receiving an SGLT2i and a GLP-1 RA, adding finerenone substantially reduced albuminuria.
CC BYText from Europe PMC. Highlighted sentences are the source of results.

Results from this study7

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone7

In this study, the peptide was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking the peptide.

  1. 01HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyEfficacy outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to reduced UACR.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to lower urine albumin versus baseline in adults with T2D and CKD.

    Outcome
    DecreaseUACR change
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Primary
    Outcome group
    Kidney function · Kidney and urinary

    Measurements

    Adjusted UACR change
    −51.3%
    Follow-up versus baseline

    Source sentences

    Summary
    Over a median follow-up of 27 weeks, the adjusted percent change in UACR was -51.3% (p < 0.001), consistent across prespecified subgroups.
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  2. 02HumanNot a test of Liraglutide aloneObservational studyEfficacy outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to reduced UACR.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to lower urine albumin versus baseline in adults with T2D and CKD.

    Outcome
    DecreaseUACR change
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Primary
    Outcome group
    Kidney function · Kidney and urinary

    Measurements

    Adjusted UACR change
    −51.3%
    Follow-up versus baseline

    Source sentences

    Summary
    Over a median follow-up of 27 weeks, the adjusted percent change in UACR was -51.3% (p < 0.001), consistent across prespecified subgroups.
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Liraglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Liraglutide.

  3. 03HumanNot a test of Semaglutide aloneObservational studyEfficacy outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to reduced UACR.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to lower urine albumin versus baseline in adults with T2D and CKD.

    Outcome
    DecreaseUACR change
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Primary
    Outcome group
    Kidney function · Kidney and urinary

    Measurements

    Adjusted UACR change
    −51.3%
    Follow-up versus baseline

    Source sentences

    Summary
    Over a median follow-up of 27 weeks, the adjusted percent change in UACR was -51.3% (p < 0.001), consistent across prespecified subgroups.
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.

  4. 04HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyEfficacy outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to reduced eGFR.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to lower eGFR versus baseline in adults with T2D and CKD.

    Outcome
    DecreaseeGFR change
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Secondary
    Outcome group
    Kidney function · Kidney and urinary

    Measurements

    Adjusted mean eGFR change
    −3.92 mL/min/1.73 m<sup>2</sup>
    Follow-up versus baseline

    Source sentences

    Summary
    The adjusted mean eGFR change was -3.92 mL/min/1.73 m2 (p < 0.001).
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  5. 05HumanNot a test of Liraglutide aloneObservational studyEfficacy outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to reduced eGFR.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to lower eGFR versus baseline in adults with T2D and CKD.

    Outcome
    DecreaseeGFR change
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Secondary
    Outcome group
    Kidney function · Kidney and urinary

    Measurements

    Adjusted mean eGFR change
    −3.92 mL/min/1.73 m<sup>2</sup>
    Follow-up versus baseline

    Source sentences

    Summary
    The adjusted mean eGFR change was -3.92 mL/min/1.73 m2 (p < 0.001).
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Liraglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Liraglutide.

  6. 06HumanNot a test of Semaglutide aloneObservational studyEfficacy outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to reduced eGFR.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to lower eGFR versus baseline in adults with T2D and CKD.

    Outcome
    DecreaseeGFR change
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Secondary
    Outcome group
    Kidney function · Kidney and urinary

    Measurements

    Adjusted mean eGFR change
    −3.92 mL/min/1.73 m<sup>2</sup>
    Follow-up versus baseline

    Source sentences

    Summary
    The adjusted mean eGFR change was -3.92 mL/min/1.73 m2 (p < 0.001).
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.

  7. 07HumanNot a test of Dulaglutide (Trulicity) aloneObservational studySafety outcome

    In adults with T2D and CKD, adding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to increased serum potassium.

    In plain wordsAdding finerenone to pooled SGLT2i and GLP-1RA therapy was linked to higher potassium versus baseline in adults with T2D and CKD.

    Outcome
    IncreaseSerum potassium
    Study

    n = 51

    Comparator
    Baseline
    Analysis
    Secondary
    Outcome group
    Adverse events · Kidney and urinary

    Measurements

    Serum potassium change
    0.34 mmol/L
    Follow-up versus baseline

    Source sentences

    Summary
    Serum potassium increased by +0.34 mmol/L (p < 0.001).
    2 context sentences
    Summary · context
    We performed a retrospective cohort study of adults with T2D and CKD from Maccabi Healthcare Services diabetes, endocrinology, and nephrology clinics in Haifa, Israel.
    Summary · context
    We aimed to assess the effectiveness of adding finerenone to existing sodium-glucose cotransporter-2 inhibitor (SGLT2i) and GLP-1 RA therapy in a real-world setting.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 4Current

    22 Oct 2026, 02:25 UTC

    Study results updated

  2. Versions 2 to 3

    21 Oct 2026, 18:59 UTC

    The same notice was added 2 times, first on 9 Oct 2026, 03:06 UTC. The status did not change between them.

    Study data updated · source update from Europe PMC

  3. Version 1

    9 Oct 2026, 03:05 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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