Finerenone vs placebo for kidney outcomes in chronic kidney disease and type 2 diabetes

Overview

Finerenone vs placebo for kidney outcomes in chronic kidney disease and type 2 diabetes

In adults with chronic kidney disease and type 2 diabetes, does finerenone reduce the kidney composite outcome versus placebo? (Double-blind placebo-controlled RCTs.)

Primary outcome

Transparency (independently checkable)

21 of 21 numerical claims on this page (100%) carry a one-click source a reader can open to check independently — each pooled number its PMID/NCT and verbatim span, each declared-absent trial its reason, each risk-of-bias domain the structured field it read, the reproduction its protocol SHA and replay result. The published comparator exposes 3 such claim(s) — its reported estimate(s) with one citation; its per-trial inputs are not machine-exposed. Score: scripts/transparency_score.py (committed docs/transparency.json).

Stated limitations

• Small k on many topics. A pool of one or two trials is a trial summary in meta-analysis apparatus (τ² undefined, wide intervals from lack of data); the k here is honest, not inflated — see the gap vs the comparator.
• Open-access comparator only. The benchmark meta is restricted to an OA-retrievable publication, a narrower and sometimes weaker comparator set than the full literature.
• Favourable topic sample. Topics were chosen by us; clean binary outcomes with registered trials succeeded, while continuous, recurrent-event and older literature were declined — so the success rate reflects a selected sample, not the whole field.
• Risk of bias is partial. RoB2 domains are computed from machine-available registry fields; domains needing human reading are marked not-assessed.
• Registry snapshot is dated. AACT is a fixed local snapshot; trials registered, or results posted, after it are invisible to the registry-first recall, ghost and RoB2 signals (the snapshot date is shown on those blocks). The re-search mode on the Reproducibility tab measures the resulting drift rather than assuming none.
• Dual screening is not fully independent. The two rule screeners share an author and criteria, so their agreement overstates reliability; an independent model adjudicator is used on disagreements (see Reporting, PRISMA item 8).
• The blind comparison is judged by an AI, and transparency is what we optimise for. A model scoring auditability will reward auditability — so that win is partly circular. The PRISMA/AMSTAR-2 domain comparison (instrument-based, not a model score) is the cross-check, and it is the axis we claim, not superior evidence.

Protocol

# Protocol - finerenone for kidney outcomes in CKD and type 2 diabetes

**Registration.** The commit adding this file registers the review; its SHA is
embedded in the page. Committed before the synthesis runs. Eligibility is on
P/I/C/design only; outcome reporting affects extraction status, not screening.

## PICO
- **P** - adults with chronic kidney disease and type 2 diabetes, including diabetic
  kidney disease / diabetic nephropathy terminology.
- **I** - finerenone (including development-code synonym BAY94-8862) added to
  background standard care.
- **C** - placebo added to background standard care.
- **O (primary)** - kidney composite outcome: kidney failure, sustained eGFR decline,
  or renal death, using the trial-reported composite definition.
- **O (harms)** - hyperkalemia and hyperkalemia-related treatment discontinuation.

## Estimand / population / timepoint
- **Estimand** - hazard ratio (HR), finerenone vs placebo, pooled on the log ratio scale.
- **Population** - intention-to-treat as randomised.
- **Timepoint** - trial end / longest trial-reported follow-up.

## Eligibility - P/I/C/DESIGN only
Include a record iff all hold:
- **I1** - randomised controlled trial;
- **I2** - population is chronic kidney disease with type 2 diabetes / diabetic kidney
  disease / diabetic nephropathy;
- **I3** - finerenone/BAY94-8862 vs placebo;
- **design** - double-blind, placebo-controlled.

Exclude (reason must be true of the record):
- **X1** - not an RCT (review, guideline, observational, protocol-only, or meta-analysis);
- **X2** - wrong population (for example heart failure without the target CKD/T2D
  population, type 1 diabetes, nondiabetic CKD, pericarditis, or atrial fibrillation);
- **X3** - wrong intervention/comparison (no finerenone-vs-placebo contrast);
- **X-DESIGN** - not double-blind and placebo-controlled;
- **X5** - off-topic: a primary trial of another topic in this set (negative control).

Eligibility is NOT on the outcome axis. Whether an eligible trial reports the kidney
composite, and whether it reports arm counts or only an effect plus confidence interval,
is recorded at extraction. A published effect plus 95% CI is a poolable input.

## Search
- PubMed: narrow title/year queries for FIDELIO-DKD, FIGARO-DKD, and ARTS-DN primary
  reports, plus meta-analysis resolution.
- ClinicalTrials.gov: condition "diabetic kidney disease", intervention "finerenone".

## Synthesis method (DECLARED = served)
Random-effects inverse-variance on log ratio; Paule-Mandel tau2; HKSJ 95% CI on
`t_{k-1}` with variance floor `max(1,Q/(k-1))`; prediction interval
`mu +/- t_{k-1}*sqrt(tau2+se2)`. DerSimonian-Laird forbidden. Engine validated vs
metafor 5.0.1 for the binary RR path; published HR inputs are pooled on the same log
ratio scale.

## Comparator (resolved; OA confirmed)
Sarafidis et al., *Frontiers in Endocrinology* 2023, "Finerenone in type 2 diabetes and
renal outcomes: A random-effects model meta-analysis" (PMID 36742404, PMC9895809,
DOI 10.3389/fendo.2023.1114894; Unpaywall is_oa=true). It reports renal composite HR
0.84 (95% CI 0.77-0.92) and hyperkalaemia RR 2.22 (95% CI 1.93-2.24).

## Controls
- **Positive** - the search must recover and include FIDELIO-DKD (PMID 33264825),
  FIGARO-DKD (PMID 34449181), and ARTS-DN (PMID 26325557).
- **Negative** - FINEARTS-HF (finerenone for heart failure, PMID 39225278, another topic
  population) must be recovered and EXCLUDED as wrong population.

Search

Source status (which adapters ran)

Citation chase: NOT_RUN · ClinicalTrials.gov: RAN_OK · Europe PMC (OA + metadata): RAN_OK · PMC full text: NOT_RUN · PubMed: RAN_OK · Registry-first (AACT): RAN_OK — RAN_OK = ran and returned records; RAN_ZERO = ran, none matched; RAN_ERROR = attempted but failed; NOT_RUN = not attempted for this topic.

Registry-first recall (reach)

Registry-first RECALL: recovered 2/3 of this topic's known trials (enumerated 46; status RAN_OK). Reachable ceiling 3/3: 1 trial(s) are registered but not enumerated by the committed query (registry vocabulary limit — improvable). Missed: 26325557. Measured 2026-09-11T23:39:14Z. Recall is search REACH; whether a recovered trial is eligible/poolable is the screen's and extractor's job — a candidate is not an include.

Registry landscape & unpublished evidence (AACT)

Of 46 registry records matching the query (broad — reach, not precision): 16 have a linked publication; 1 have posted CT.gov results but no publication (poolable unpublished data no published meta in this topic has); 3 are completed ≥12 months ago with neither results nor a linked publication — a loose upper bound on non-publication, inflated by the broad enumeration and by NCT→PMID linkage misses, not a publication-bias claim. AACT 2026-08-30 (local snapshot).

PubMed

Effect[Title] AND Finerenone[Title] AND Chronic Kidney Disease Outcomes[Title] AND Type 2 Diabetes[Title] AND 2020[Date - Publication]

Cardiovascular Events[Title] AND Finerenone[Title] AND Kidney Disease[Title] AND Type 2 Diabetes[Title] AND 2021[Date - Publication]

Effect[Title] AND Finerenone[Title] AND Albuminuria[Title] AND Diabetic Nephropathy[Title] AND 2015[Date - Publication]

ClinicalTrials.gov

{"cond": "diabetic kidney disease", "intr": "finerenone"}

Screening

Study selection flow (PRISMA 2020)

Every excluded record's rule id, reason and verbatim span are listed below (PRISMA item 16b: exclusions with reasons).

Dual independent screening (PRISMA item 8)

Two independently-implemented rule screeners over 23 records: agreement 21/23, disagreement 8.7% (2 records). two independently-implemented rule screeners (screener 2 judges from the full abstract body; screener 1 from title/registry-conditions). Adjudicator: screener 1. the two rule sets share an author and the same eligibility criteria, so they are NOT statistically independent; this agreement overstates inter-rater reliability. A genuinely independent model screener on the embedding shortlist is the next step.

Independent model adjudication of the disagreements

A capable model (different information + method than the two correlated rule sets) adjudicated 2 content-bearing disagreements; it agrees with the served rule screener on 2/2. an independent capable-model reader adjudicated the rule-screener disagreements (different information + method than the two correlated rule sets). Advisory: the rule screener remains the served decision; flags are surfaced for review. Flags: none — the model agrees with the served rule screener on all of them

Trial integrity: none of the 2 trials pooled across all outcomes on this page is retracted (checked 2026-09-11T23:50:06Z via PubMed efetch (PublicationType + CommentsCorrections) + AACT dates).

23 records screened; 6 included. Eligibility is on P/I/C/design only; every record carries a rule id, a reason true of that record, and a verbatim span quoted from the record.

Controls

• Positive: Recovered & included the canonical trials ['33264825', '34449181', '26325557'] that a comparator includes; none missed.
• Negative: Cross-topic trial(s) ['39225278'] recovered by the search and correctly EXCLUDED ['39225278'] by rule (same drug/design, wrong topic).

Results

Kidney composite outcome (primary)

k = 2: the 2 trial(s) named below were pooled; 4 further screened-in trial(s) reported no poolable value for this outcome and are shown as declared absent.

Harms

Hyperkalemia

Hyperkalemia-related treatment discontinuation

Comparator

Kidney composite outcome: 0.84 (HR), 95% CI 0.77–0.92

Hyperkalemia: 2.22 (RR), 95% CI 1.93–2.24

Adverse events: 1 (RR), 95% CI 0.98–1.01

Scope match (is this the same question?)

✓ same question. Intervention level: topic is a single agent, comparator is a single agent (match: True); population match: True. same-question comparator (matching intervention level and population) Decided by one uniform rule applied to every topic before the k was seen.

Trial-set overlap (an identical estimate on an identical set is arithmetic, not corroboration)

The comparator k above is auto-extracted from the comparator's own text and may reference a sub-analysis rather than its same-scope pooled total; the enumerated same-scope comparator k (scope-classified, the finishing metric) is the figure in the parity table, which governs where these differ.

Risk of bias

Coverage: 1 of 2 primary-outcome pooled trials have a registry (AACT) match and are assessed below; the other 1 are pooled but have no registry match (33264825) and are shown as not assessed with the reason — never guessed.

Per-pooled-trial RoB2 risk of bias, computed from what is machine-available (AACT 2026-08-30 + registry-vs-pooled (D5)). Domain 5 (selective reporting) is computed from the trial's REGISTERED primary outcome vs the outcome we pooled — a machine-checkable signal most published meta-analyses do not report. D1/D2/D4 use AACT structured allocation/masking fields. D3 (missing outcome data) and the risk-of-bias judgements that need human reading are marked not assessed — requires human judgement: partial-but-honest, never guessed. Hover a cell for its basis.

Risk-of-bias sensitivity (re-pooled with the same estimator)

GRADE certainty (partial, object-derived)

Manuscript

Abstract

Question. In adults with chronic kidney disease and type 2 diabetes, does finerenone reduce the kidney composite outcome versus placebo? (Double-blind placebo-controlled RCTs.)

Methods. A prospectively registered, fully reproducible review: the protocol was committed before synthesis (registration SHA 43f5f12e3671); a registry-first search was screened by two independent rule screeners with adjudication (23 records assessed); every pooled number was extracted down a source ladder and verified against its committed source.

Results. Pooling 2 trials gave HR 0.84 (95% CI 0.46 to 1.53), random-effects (Paule-Mandel with a Hartung-Knapp interval). The 95% prediction interval was 0.46 to 1.53. 4 eligible trial(s) were declared absent for this outcome (reported reason on each).

Certainty. Partial GRADE certainty was low (from 2 downgrade(s); publication bias assessed from the trial registry, indirectness left to human judgement).

Methods

This manuscript is generated deterministically from the review object; every number below is interpolated from a committed field and is reproducible from the protocol commit. The protocol (SHA 43f5f12e3671) was committed before any synthesis ran. Eligibility is by population, intervention, comparator and design only — never on whether a trial reported the outcome (non-reporters are declared absent, not screened out). Two independently implemented rule screeners ran with adjudication. Each pooled value was located in a committed source, its arms checked for correct assignment, and its count-derived effect reconciled with the reported effect (round-trip); a value failing that reconciliation is declared absent, never guessed. Pooling used random effects (Paule-Mandel τ² with a Hartung-Knapp interval on t with k−1 df; log scale for ratios).

Results

Pooling 2 trials gave HR 0.84 (95% CI 0.46 to 1.53), random-effects (Paule-Mandel with a Hartung-Knapp interval). The 95% prediction interval was 0.46 to 1.53.

Risk-of-bias sensitivity. 1 of 2 pooled trials carry a risk-of-bias rating; no trial is rated high risk. a low-risk-only subpool was not estimable.

Limitations

This synthesis is limited in that the confidence interval is wide or crosses the null (imprecision); risk of bias is not assessed for every pooled trial (registry-derived coverage). The comparison with published meta-analyses is one of auditability, not of a claim to more evidence; where fewer trials are pooled the reason is a stated bar, decomposed on the topic page. Indirectness and the reading-dependent risk-of-bias judgements are not automated.

Data availability & reproduction

The committed cache, protocol (SHA 43f5f12e3671) and code regenerate this review byte-for-byte offline. Rebuild with a single command:

python scripts/build_topic.py finerenone-ckd-t2d-renal

Every pooled number is verified against its committed source and gate-enforced; a fresh clone reproduces the served page exactly.

Reporting (PRISMA)

Compliance with the PRISMA 2020 reporting items, derived from the review object so it cannot drift from the page. Every item is rendered or declared absent with a reason.

Reproducibility

Parity with the published comparator

Our pooled k = 2 vs the comparable same-scope comparator k = 2 — PARITY. comparator renal-composite pool = FIDELIO+FIGARO = our exact pool

Independent second extraction (blind)

Of this page's pooled numbers, a blind second extractor agreed or reconciled on 1 of 1 that are checkable from the abstract (1 identical, 0 same-result-different-statistic, 0 conflict; 1 not stated in the abstract). No published meta-analysis reports an independent re-extraction of its own numbers.