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Clinical stage molecule PT150 is a modulator of glucocorticoid and androgen receptors with antiviral activity against SARS-CoV-2.
Theise, Neil D; Arment, Anthony R; Chakravarty, Dimple; Gregg, John M H; Jacobson, Ira M; Jung, Kie Hoon; Nair, Sujit S; Tewari, Ashutosh K; Thurston, Archie W; Van Drie, John; Westover, Jonna B.
  • Theise ND; Department of Pathology, New York University-Grossman School of Medicine , New York, NY, USA.
  • Arment AR; Palisades Therapeutics/Pop Test Oncology LLC , Cliffside Park, NJ, USA.
  • Chakravarty D; Department of Biology, Central State University , Wilberforce, OH, USA.
  • Gregg JMH; Department of Urology and the Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY, USA.
  • Jacobson IM; Palisades Therapeutics/Pop Test Oncology LLC , Cliffside Park, NJ, USA.
  • Jung KH; Department of Medicine, New York University-Grossman School of Medicine , New York, NY, USA.
  • Nair SS; Department of Animal, Dairy, and Veterinary Sciences, Utah State University , Logan, UT, USA.
  • Tewari AK; Department of Urology and the Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY, USA.
  • Thurston AW; Department of Urology and the Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY, USA.
  • Van Drie J; ADME Solutions, Inc , San Diego, CA, USA.
  • Westover JB; Van Drie Research , North Andover, MA, USA.
Cell Cycle ; 19(24): 3632-3638, 2020 12.
Article in English | MEDLINE | ID: covidwho-1066164
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Receptors, Androgen / Receptors, Glucocorticoid / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Prognostic study Limits: Humans Language: English Journal: Cell Cycle Year: 2020 Document Type: Article Affiliation country: 15384101.2020.1859752

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Receptors, Androgen / Receptors, Glucocorticoid / SARS-CoV-2 / COVID-19 Drug Treatment Type of study: Prognostic study Limits: Humans Language: English Journal: Cell Cycle Year: 2020 Document Type: Article Affiliation country: 15384101.2020.1859752