Evidence map›Paper›PMID 35163378›Full record

ReviewInternational journal of molecular sciences2022

Current Knowledge about the New Drug Firibastat in Arterial Hypertension.

Emma Hansen, Daniela Grimm, Markus Wehland

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Emerging therapeutic frontiers in hypertension management.Frontiers in cardiovascular medicine · 2025
    Review
  3. Therapeutic Potential ofPharmaceuticals (Basel, Switzerland) · 2023
    Review
  4. 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

3 authors at 2 institutions in 2 countries.

Emma HansenDepartment of Biomedicine, Aarhus University, Ole Worms Allé 4, 8000 Aarhus, Denmark.
Daniela GrimmDepartment of Biomedicine, Aarhus University, Ole Worms Allé 4, 8000 Aarhus, Denmark.ORCID 0000-0002-4991-3105
Markus WehlandDepartment of Microgravity and Translational Regenerative Medicine, Otto von Guericke University, Universitätsplatz 2, Building 28, 39106 Magdeburg, Germany.ORCID 0000-0002-8160-859X
Aarhus University · DKOtto-von-Guericke-Universität Magdeburg · DE

Funding

German Aerospace Center 50WB1524German Aerospace Center 50WB1924
6 · The paper itself

Abstract

Hypertension significantly increases the risk of cardiovascular disease. Currently, effective standard pharmacological treatment is available in the form of diuretics, ACE inhibitors, angiotensin II receptor blockers and calcium channel blockers. These all help to decrease blood pressure in hypertensive patients, each with their own mechanism. Recently, firibastat, a new first-in-class antihypertensive drug has been developed. Firibastat is a prodrug that when crossing the blood-brain barrier, is cleaved into two active EC33 molecules. EC33 is the active molecule that inhibits the enzyme aminopeptidase A. Aminopeptidase A converts angiotensin II to angiotensin III. Angiotensin III usually has three central mechanisms that increase blood pressure, so by inhibiting this enzyme activity, a decrease in blood pressure is seen. Firibastat is an antihypertensive drug that affects the brain renin angiotensin system by inhibiting aminopeptidase A. Clinical trials with firibastat have been performed in animals and humans. No severe adverse effects related to firibastat treatment have been reported. Results from studies show that firibastat is generally well tolerated and safe to use in hypertensive patients. The aim of this review is to investigate the current knowledge about firibastat in the treatment of hypertension.

Indexed as

AnimalsArteriesClinical Trials as TopicDisulfidesHumansHypertensionProdrugsRenin-Angiotensin SystemSulfonic AcidsDisulfidesfiribastatProdrugsSulfonic Acidsbrain RASfiribastathypertension

Identifiers

PMID35163378
PMCPMC8836050
OpenAlexW4210775118

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.