Evidence map›Paper›PMID 40702159›Full record

ArticleScientific reports2025

Topical ophthalmic administration of the antiangiogenic peptide VIAN-c4551 protects against experimental diabetic macular edema.

Elva Adán-Castro, Magdalena Zamora, Daniela Granados-Carrasco, Lourdes Siqueiros-Márquez, Jose F García-Rodrigo, Fernando Macias, Thomas Bertsch, Jakob Triebel, Edith Arnold, Gonzalo Martínez de la Escalera and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. 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. Article
  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

12 authors.

Elva Adán-Castro *Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Magdalena Zamora *Instituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Daniela Granados-CarrascoInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Lourdes Siqueiros-MárquezInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Jose F García-RodrigoInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Fernando MaciasInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Thomas BertschInstitute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, Nuremberg General Hospital & Paracelsus Medical University, Nuremberg, Germany.
Jakob TriebelInstitute for Clinical Chemistry, Laboratory Medicine and Transfusion Medicine, Nuremberg General Hospital & Paracelsus Medical University, Nuremberg, Germany.
Edith ArnoldInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Gonzalo Martínez de la EscaleraInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México.
Juan Pablo RoblesInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México. jp.robles@viantx.com.
Carmen ClappInstituto de Neurobiología, Universidad Nacional Autónoma de México (UNAM), Querétaro, 76230, Qro, México. clapp@unam.mx.

Funding

Secretaría de Educación, Ciencia, Tecnología e Innovación de la Ciudad de México SECTEI/061/2023
6 · The paper itself

Abstract

Increased angiogenesis and vascular permeability are hallmarks of microvascular retinal diseases such as diabetic retinopathy and diabetic macular edema (DME). Periodic intravitreal injections of inhibitors of the vascular endothelial growth factor (VEGF) are first-line therapy, but their invasiveness and associated risks often lead to poor compliance and outcomes. Here, we investigate VIAN-c4551, a highly potent antiangiogenic cyclic heptapeptide, as a non-invasive topical ophthalmic alternative to the current standard of care for DME. VIAN-c4551 demonstrated high potency (IC

Indexed as

Angiogenesis InhibitorsDiabetic RetinopathyMacular EdemaPeptides, CyclicAdministration, OphthalmicAnimalsCapillary PermeabilityDiabetes Mellitus, ExperimentalDogsHumansHuman Umbilical Vein Endothelial CellsMadin Darby Canine Kidney CellsMaleMiceOphthalmic SolutionsRabbitsAngiogenesis InhibitorsOphthalmic SolutionsPeptides, CyclicVascular Endothelial Growth Factor AAnti-angiogenesisDiabetic macular edemaDiabetic retinopathyEfficacyEye dropsPharmacokineticsTherapeutic peptideVascular permeabilityVasoinhibin analog

Identifiers

PMID40702159
PMCPMC12287436

What OpenQuestion holds

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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.