Evidence map›Paper›PMID 42108271›Full record

Trial reportNature medicine2026

The microRNA inhibitor CDR132L in patients with reduced left ventricular ejection fraction after myocardial infarction: a randomized phase 2 trial.

Johann Bauersachs, Scott D Solomon, Stefan D Anker, Isabel Antorrena-Miranda, Rudolf A de Boer, Gerasimos Filippatos, Tim Friede, Wilfried Hauke, Piotr Ponikowski, Orly Vardeny and 4 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Nature medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. RNA therapeutics: current status and future directions.Signal transduction and targeted therapy · 2026
    Review
  2. Review
  3. Review
  4. Review
  5. TheNon-coding RNA · 2026
    Article
  6. Article
  7. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Johann Bauersachs *Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0000-0002-9341-117X
Scott D Solomon *Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-3698-9597
Stefan D AnkerDepartment of Cardiology (CVK) of German Heart Center Charité; German Centre for Cardiovascular Research (DZHK), partner site Berlin, Charité Universitätsmedizin, Berlin, Germany.ORCID http://orcid.org/0000-0002-0805-8683
Isabel Antorrena-MirandaDepartment of Cardiology, La Paz University Hospital, Research Institute IdiPAZ, Madrid, Spain.ORCID http://orcid.org/0000-0001-9523-3787
Rudolf A de BoerDepartment of Cardiology, Erasmus University Medical Centre, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-4775-9140
Gerasimos FilippatosDepartment of Cardiology, Athens University Hospital Attikon, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Tim FriedeDepartment of Medical Statistics, University Medical Centre Göttingen, Göttingen, Germany.ORCID http://orcid.org/0000-0001-5347-7441
Wilfried HaukeCardior Pharmaceuticals GmbH, a Novo Nordisk company, Hannover, Germany.
Piotr PonikowskiInstitute of Heart Diseases, University Hospital, Medical University Wroclaw, Wroclaw, Poland.
Orly VardenyUniversity of Minnesota Medical School, Minneapolis, MN, USA.ORCID http://orcid.org/0000-0002-6387-1351
Rebecca AltschulNovo Nordisk A/S, Søborg, Denmark.
Michael GamborgNovo Nordisk A/S, Søborg, Denmark.
Kasper VintherNovo Nordisk A/S, Søborg, Denmark.
Thomas ThumCardior Pharmaceuticals GmbH, a Novo Nordisk company, Hannover, Germany. thum.thomas@mh-hannover.de.ORCID http://orcid.org/0000-0003-4360-1511

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNA-132 (miR-132) is a central regulator of adverse cardiac remodeling. Here we evaluated CDR132L, a synthetic antisense oligonucleotide miR-132 inhibitor, in a multinational, randomized, double-blind, placebo-controlled phase 2 trial (HF-REVERT) in patients with recent myocardial infarction (MI) and left ventricular (LV) systolic dysfunction. Within 3-14 days after MI, 294 patients were randomized to receive CDR132L 5 mg kg

Indexed as

MicroRNAsMyocardial InfarctionOligonucleotides, AntisenseStroke VolumeVentricular Dysfunction, LeftAgedDouble-Blind MethodFemaleHumansMaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsVentricular RemodelingMicroRNAsMIRN132 microRNA, humanNatriuretic Peptide, BrainOligonucleotides, AntisensePeptide Fragmentspro-brain natriuretic peptide (1-76)

Identifiers

PMID42108271
PMCPMC13375544

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.