Initial Changes in eGFR during Treatment with Balcinrenone and Dapagliflozin

INTRODUCTION: The novel non-steroidal mineralocorticoid receptor antagonist balcinrenone in combination with dapagliflozin reduced urinary albumin-to-creatinine ratio (UACR) over 12 weeks in the MIRO-CKD phase 2 trial in chronic kidney disease (CKD) and induced a modest acute eGFR reduction upon treatment initiation. This pre-specified analysis explored the acute eGFR changes in response to balcinrenone/dapagliflozin and the association of these acute eGFR changes on safety and efficacy parameters. METHODS: Adults with CKD (n=324, eGFR ≥25 to <60 mL/min/1.73m2; UACR ≥100 to <5000 mg/g) were randomized to balcinrenone/dapagliflozin 15/10 mg, balcinrenone/dapagliflozin 40/10 mg, or dapagliflozin 10 mg/placebo as adjunct to renin-angiotensin-system therapy. The primary outcome was the relative change in UACR from baseline over 12 weeks. Acute eGFR changes 4 weeks post-randomization and 4 weeks post-treatment were assessed using mixed model repeated measures. We categorized participants according to relative eGFR changes: ≥10% reduction (eGFR dip); >0 to <10% reduction; or an eGFR increase. We examined safety and concomitant changes in systolic blood pressure (SBP) and UACR across categories of eGFR changes. RESULTS: Relative to dapagliflozin/placebo, the acute eGFR dip at Week 4 with balcinrenone/dapagliflozin 15/10 mg was -0.6 mL/min/1.73m2 (95%CI: -2.4, 1.1) and with balcinrenone/dapagliflozin 40/10 mg -1.7 mL/min/1.73m2 (95%CI -3.5, -0.01). The acute reduction in eGFR with balcinrenone/dapagliflozin was reversible 4 weeks after treatment discontinuation. This finding was consistent across subgroups. In the overall cohort, larger acute eGFR reductions were associated with larger reductions in UACR and SBP across treatment arms. Rates of serious adverse events and adverse events of special interest were low, similar in the balcinrenone/dapagliflozin versus placebo/dapagliflozin group, and unrelated to the acute eGFR change. CONCLUSION: In adults with CKD, balcinrenone/dapagliflozin induced a modest acute eGFR reduction which was reversible after treatment discontinuation, did not lead to increased rates of adverse events, and was associated with greater SBP and UACR lowering.

Authors

Institutions

Publication Details

Journal
Clinical Journal of the American Society of Nephrology
Published
2026-09-17
DOI
https://doi.org/10.2215/cjn.0000001202
Primary Topic
Hormonal Regulation and Hypertension
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

Initial Changes in eGFR during Treatment with Balcinrenone and Dapagliflozin

Özkan Güngör, Maria Leonsson‐Zachrisson, Nicolás Guzmán, Erika De Sousa Amorim et al.
Clinical Journal of the American Society of Nephrology
Hormonal Regulation and Hypertension
article

Initial Changes in eGFR during Treatment with Balcinrenone and Dapagliflozin

Özkan Güngör, Maria Leonsson‐Zachrisson, Nicolás Guzmán, Erika De Sousa Amorim, Hiddo J.L. Heerspink, Jelle M. Beernink, Patrick B. Mark, Yunyun Jiang, Anna L. Eriksson, Martin Fredholm, Judith Hartleib-Geschwindner
article en

Abstract

INTRODUCTION: The novel non-steroidal mineralocorticoid receptor antagonist balcinrenone in combination with dapagliflozin reduced urinary albumin-to-creatinine ratio (UACR) over 12 weeks in the MIRO-CKD phase 2 trial in chronic kidney disease (CKD) and induced a modest acute eGFR reduction upon treatment initiation. This pre-specified analysis explored the acute eGFR changes in response to balcinrenone/dapagliflozin and the association of these acute eGFR changes on safety and efficacy parameters. METHODS: Adults with CKD (n=324, eGFR ≥25 to <60 mL/min/1.73m2; UACR ≥100 to <5000 mg/g) were randomized to balcinrenone/dapagliflozin 15/10 mg, balcinrenone/dapagliflozin 40/10 mg, or dapagliflozin 10 mg/placebo as adjunct to renin-angiotensin-system therapy. The primary outcome was the relative change in UACR from baseline over 12 weeks. Acute eGFR changes 4 weeks post-randomization and 4 weeks post-treatment were assessed using mixed model repeated measures. We categorized participants according to relative eGFR changes: ≥10% reduction (eGFR dip); >0 to <10% reduction; or an eGFR increase. We examined safety and concomitant changes in systolic blood pressure (SBP) and UACR across categories of eGFR changes. RESULTS: Relative to dapagliflozin/placebo, the acute eGFR dip at Week 4 with balcinrenone/dapagliflozin 15/10 mg was -0.6 mL/min/1.73m2 (95%CI: -2.4, 1.1) and with balcinrenone/dapagliflozin 40/10 mg -1.7 mL/min/1.73m2 (95%CI -3.5, -0.01). The acute reduction in eGFR with balcinrenone/dapagliflozin was reversible 4 weeks after treatment discontinuation. This finding was consistent across subgroups. In the overall cohort, larger acute eGFR reductions were associated with larger reductions in UACR and SBP across treatment arms. Rates of serious adverse events and adverse events of special interest were low, similar in the balcinrenone/dapagliflozin versus placebo/dapagliflozin group, and unrelated to the acute eGFR change. CONCLUSION: In adults with CKD, balcinrenone/dapagliflozin induced a modest acute eGFR reduction which was reversible after treatment discontinuation, did not lead to increased rates of adverse events, and was associated with greater SBP and UACR lowering.

Clinical Journal of the American Society of Nephrology
University Medical Center Groningen (NL), AstraZeneca (Poland) (PL), AstraZeneca (Finland) (FI), AstraZeneca (Italy) (IT), AstraZeneca (Spain) (ES), Kahramanmaraş Sütçü İmam University (TR), University of Glasgow (GB)
Good health and well-being
Openalex Percentile: Top 11%
Hormonal Regulation and Hypertension
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.