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Record W4415434951 · doi:10.1093/ndt/gfaf116.1970

#644 A phase 2b dose finding study to assess the efficacy of RMC-035 on renal function in participants at high risk for kidney injury following open-chest cardiac surgery (POINTER)

2025· article· en· W4415434951 on OpenAlexaffabout
Alexander Zarbock, Tobias Agervald, Michael Reusch, Maxime Laflamme, Andrej Myjavec, C David Mazer, Benoît de Varennes, Johannes Boehm

Bibliographic record

VenueNephrology Dialysis Transplantation · 2025
Typearticle
Languageen
FieldMedicine
TopicAcute Kidney Injury Research
Canadian institutionsSt. Michael's HospitalRoyal Victoria HospitalUniversité LavalInstitut universitaire de cardiologie et de pneumologie de Québec
Fundersnot available
KeywordsClinical endpointRenal functionAdverse effectAcute kidney injuryCardiac surgeryKidney diseaseCardiopulmonary bypassKidney

Abstract

fetched live from OpenAlex

Abstract Background and Aims Acute kidney injury (AKI) is a common and serious complication of cardiac surgery, potentially leading to the onset or progression of CKD. There are no approved pharmacotherapies for the prevention of AKI or the subsequent development or progression of CKD. RMC-035, a therapeutic variant of the endogenous protein alpha-1-microglobulin, demonstrates nephroprotective effects in numerous preclinical disease models1. Results from the Phase 2a AKITA trial2 indicate that RMC-035 improves long-term kidney outcomes after cardiac surgery. The Phase 2b POINTER trial aims to confirm the findings from AKITA and identify the optimal RMC-035 dose prior to initiating a pivotal Phase 3 study. Method POINTER (NCT06475274) is an international, multicenter, randomized, placebo-controlled, double-blind trial. A total of approximately 160 high-risk patients scheduled for open-chest cardiac surgery with cardiopulmonary bypass (CPB) will be recruited in Europe and Canada. Two RMC-035 dose levels (30 and 60 mg) will be compared with placebo. Study drug will be administered by IV infusion 10 min before CPB, and at 6- and 24-h post-surgery. Patients will be followed daily until day 4, and on days 7, 60, and 90. The primary endpoint is the change in eGFR at day 90 compared to baseline. A key secondary endpoint is major adverse kidney events on day 90 (MAKE90). Other secondary endpoints include the occurrence of AKI, and plasma concentrations of RMC-035. Safety will be assessed by treatment-emergent adverse events, vital signs, electrocardiogram and routine blood biochemistry and hematology parameters. Results Not applicable. Conclusion In the completed AKITA trial, RMC-035 improved eGFR by day 90 vs placebo, and fewer patients treated with RMC-035 met the secondary MAKE90 endpoint. The eGFR benefit was more pronounced in the predefined subgroup of patients with lower preoperative eGFR (<60 mL/min/1.73 m²). Herein, we present the design of the Phase 2b POINTER trial, aimed at determining the optimal dosing regimen of RMC-035 and confirming its nephroprotective properties prior to a Phase 3 trial. The results are expected to advance our understanding of novel therapeutic strategies for the prevention of AKI and permanent loss of renal function in patients at high risk for AKI following cardiac surgery.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.003
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.015
Threshold uncertainty score0.051

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0030.002
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0030.002
Bibliometrics0.0000.000
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0010.000
Research integrity0.0030.004
Insufficient payload (model declined to judge)0.0150.002

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.068
GPT teacher head0.399
Teacher spread0.330 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes2
Has abstractyes

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