Evidence map›Paper›PMID 33305659›Full record

ArticleCell cycle (Georgetown, Tex.)2020

Clinical stage molecule PT150 is a modulator of glucocorticoid and androgen receptors with antiviral activity against SARS-CoV-2.

Neil D Theise, Anthony R Arment, Dimple Chakravarty, John M H Gregg, Ira M Jacobson, Kie Hoon Jung, Sujit S Nair, Ashutosh K Tewari, Archie W Thurston, John Van Drie and 1 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04761107 (Mitigating Risk of COVID-19 for Clinical Management of Genitourinary Diseases), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 44% 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.

NCT04761107 active not recruitingnot on this mapstarted 2021, after this paper: background citation

Mitigating Risk of COVID-19 for Clinical Management of Genitourinary Diseases

TypeobservationalSponsorIcahn School of Medicine at Mount SinaiRan2021 to 2026Enrolled15,240ConditionsCOVID-19 Infection, Genitourinary Cancer, Benign Urologic Conditions
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  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

11 authors at 4 institutions in 1 country.

Neil D TheiseDepartment of Pathology, New York University-Grossman School of Medicine , New York, NY, USA.ORCID 0000-0002-4048-5140
Anthony R ArmentDepartment of Biology, Central State University , Wilberforce, OH, USA.
Dimple ChakravartyDepartment of Urology and the Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY, USA.
John M H GreggPalisades Therapeutics/Pop Test Oncology LLC , Cliffside Park, NJ, USA.
Ira M JacobsonDepartment of Medicine, New York University-Grossman School of Medicine , New York, NY, USA.
Kie Hoon JungDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University , Logan, UT, USA.
Sujit S NairDepartment of Urology and the Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY, USA.
Ashutosh K TewariDepartment of Urology and the Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY, USA.
Archie W ThurstonADME Solutions, Inc , San Diego, CA, USA.
John Van DrieVan Drie Research , North Andover, MA, USA.
Jonna B WestoverDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University , Logan, UT, USA.
Icahn School of Medicine at Mount Sinai · USNew York University · USUtah State University · USCentral State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PT150 is a clinical-stage molecule, taken orally, with a strong safety profile having completed Phase 1 and Phase 2 clinical trials for its original use as an antidepressant. It has an active IND for COVID-19. Antiviral activities have been found for PT150 and other members of its class in a variety of virus families; thus, it was now tested against SARS-CoV-2 in human bronchial epithelial lining cells and showed effective 90% inhibitory antiviral concentration (EC90) of 5.55 µM. PT150 is a member of an extended platform of novel glucocorticoid receptor (GR) and androgen receptor (AR) modulating molecules. In vivo, their predominant net effect is one of systemic glucocorticoid antagonism, but they also show direct downregulation of AR and minor GR agonism at the cellular level. We hypothesize that anti-SARS-CoV-2 activity depends in part on this AR downregulation through diminished TMPRSS2 expression and modulation of ACE2 activity. Given that hypercortisolemia is now suggested to be a significant co-factor for COVID-19 progression, we also postulate an additive role for its potent immunomodulatory effects through systemic antagonism of cortisol.

Indexed as

COVID-19 Drug TreatmentAlveolar Epithelial CellsAngiotensin-Converting Enzyme 2Antiviral AgentsCell LineDisease ProgressionDown-RegulationGlucocorticoidsHumansHydrocortisoneImmunologic FactorsMiddle East Respiratory Syndrome CoronavirusReceptors, AndrogenReceptors, GlucocorticoidSARS-CoV-2Serine EndopeptidasesACE2 protein, humanAngiotensin-Converting Enzyme 2Antiviral AgentsGlucocorticoidsHydrocortisoneImmunologic FactorsReceptors, AndrogenReceptors, GlucocorticoidSerine EndopeptidasesTMPRSS2 protein, humanAndrogen receptorCOVID-19Glucocorticoid antagonistSARS-CoV-2Therapeutic

Identifiers

PMID33305659
PMCPMC7738205
OpenAlexW3111772534

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.