Evidence map›Paper›PMID 42102517›Full record

ReviewThe journal of prevention of Alzheimer's disease2026

RNA-based therapeutics for Alzheimer's disease and related tauopathies: challenges and opportunities.

Binita Rajbanshi, Ilaria Brentari, Michela Alessandra Denti, Jeffrey L Cummings, Anuj Guruacharya

Abstract readReview
In one paragraph

Review in The journal of prevention of Alzheimer's disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

5 authors.

Binita RajbanshiNanil Therapeutics Inc., San Francisco, USA. Electronic address: bini@naniltx.com.
Ilaria BrentariDepartment of Cellular, Computational and Integrative Biology, University of Trento, Trento, Italy.
Michela Alessandra DentiDepartment of Cellular, Computational and Integrative Biology, University of Trento, Trento, Italy.
Jeffrey L CummingsChambers-Grundy Center for Transformative Neuroscience, Department of Brain Health, Kirk Kerkorian School of Medicine, University of Nevada Las Vegas, Las Vegas, USA.
Anuj GuruacharyaNanil Therapeutics Inc., San Francisco, USA. Electronic address: anuj@naniltx.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tauopathies are neurodegenerative diseases characterized by pathological tau protein accumulation. Though therapies involving monoclonal antibodies and small-molecule inhibitors have progressed, they have so far failed in multiple clinical trials, underscoring the need for innovative molecular approaches. RNA-based therapies offer an alternative disease-modifying approach by being able to target tau at its molecular origin. Diverse modalities, such as mRNA, ASO, RNAi, and SSO, offer distinct promises. Though their challenges are equally diverse, they also share common problems. This review examines the nascent field of RNA therapeutics for tauopathies, outlining emerging modalities, translational barriers, molecular targets, clinical trials, and patent trends.

Indexed as

Alzheimer DiseaseGenetic TherapyRNATauopathiesAnimalsHumanstau ProteinsRNAtau ProteinsAlzheimer'sNeurodegenerationRNARNA-based therapiesTauopathiesTau targets

Identifiers

PMID42102517
PMCPMC13185650

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.