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Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19

This article summarizes the likely attenuation properties of RRx-001 in COVID-19 based on its mechanism of action and the putative pathogenesis of the disease, which appears to activate inflammatory, oxidative, and immune cascades with the potential to culminate in acute respiratory distress syndrom...

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Detalles Bibliográficos
Autores principales: Oronsky, Bryan., Knox, Susan., Cabrales, Pedro., Oronsky, Arnold., Reid, Tony R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341953/
https://www.ncbi.nlm.nih.gov/pubmed/32718560
http://dx.doi.org/10.1053/j.seminoncol.2020.07.002
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author Oronsky, Bryan.
Knox, Susan.
Cabrales, Pedro.
Oronsky, Arnold.
Reid, Tony R.
author_facet Oronsky, Bryan.
Knox, Susan.
Cabrales, Pedro.
Oronsky, Arnold.
Reid, Tony R.
author_sort Oronsky, Bryan.
collection PubMed
description This article summarizes the likely attenuation properties of RRx-001 in COVID-19 based on its mechanism of action and the putative pathogenesis of the disease, which appears to activate inflammatory, oxidative, and immune cascades with the potential to culminate in acute respiratory distress syndrome, cytokine storm and death. An ongoing pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), COVID-19 appears to present with 3 major patterns of clinical symptomatology: (1) mild upper respiratory tract infection, (2) non–life-threatening pneumonia, and (3) severe pneumonia and acute respiratory distress syndrome that initially manifest as a mild prodrome lasting for 7–8 days before rapid clinical and radiological deterioration requiring ICU transfer. RRx-001 is a targeted nitric oxide donor. This small molecule, which has been evaluated in multiple Phase 1–2 clinical trials for cancer as well as a Phase 3 clinical trial for the treatment of small cell lung cancer called REPLATINUM (NCT03699956), is minimally toxic and demonstrates clear evidence of antitumor activity. During the course of these clinical trials it was noted that the rate of chronic obstructive pulmonary disease exacerbation and pneumonia in actively smoking small cell lung cancer patients treated with RRx-001 is less than 1%. Due to extensive history of tobacco use, 40%–70% of patients with lung cancer have chronic obstructive pulmonary disease and the expected rate of pulmonary infection in this population is 50%–70%, which was not observed in RRx-001 clinical trials. Moreover, in preclinical studies of pulmonary hypertension, RRx-001 was found to be comparable with or more effective than the FDA approved agent, Bosentan. The potential pulmonary protective effects of RRx-001 in patients with recurrent lung infections coupled with preclinical models demonstrating RRx-001-mediated reversal of pulmonary hypertension suggests RRx-001 may have therapeutic activity in patients with acute respiratory symptoms due to COVID 19. Clinical trials have been initiated to confirm the hypothesis that RRx-001 may be repurposed to treat SARS-CoV-2 infection.
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spelling pubmed-73419532020-07-08 Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19 Oronsky, Bryan. Knox, Susan. Cabrales, Pedro. Oronsky, Arnold. Reid, Tony R. Semin Oncol Article This article summarizes the likely attenuation properties of RRx-001 in COVID-19 based on its mechanism of action and the putative pathogenesis of the disease, which appears to activate inflammatory, oxidative, and immune cascades with the potential to culminate in acute respiratory distress syndrome, cytokine storm and death. An ongoing pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), COVID-19 appears to present with 3 major patterns of clinical symptomatology: (1) mild upper respiratory tract infection, (2) non–life-threatening pneumonia, and (3) severe pneumonia and acute respiratory distress syndrome that initially manifest as a mild prodrome lasting for 7–8 days before rapid clinical and radiological deterioration requiring ICU transfer. RRx-001 is a targeted nitric oxide donor. This small molecule, which has been evaluated in multiple Phase 1–2 clinical trials for cancer as well as a Phase 3 clinical trial for the treatment of small cell lung cancer called REPLATINUM (NCT03699956), is minimally toxic and demonstrates clear evidence of antitumor activity. During the course of these clinical trials it was noted that the rate of chronic obstructive pulmonary disease exacerbation and pneumonia in actively smoking small cell lung cancer patients treated with RRx-001 is less than 1%. Due to extensive history of tobacco use, 40%–70% of patients with lung cancer have chronic obstructive pulmonary disease and the expected rate of pulmonary infection in this population is 50%–70%, which was not observed in RRx-001 clinical trials. Moreover, in preclinical studies of pulmonary hypertension, RRx-001 was found to be comparable with or more effective than the FDA approved agent, Bosentan. The potential pulmonary protective effects of RRx-001 in patients with recurrent lung infections coupled with preclinical models demonstrating RRx-001-mediated reversal of pulmonary hypertension suggests RRx-001 may have therapeutic activity in patients with acute respiratory symptoms due to COVID 19. Clinical trials have been initiated to confirm the hypothesis that RRx-001 may be repurposed to treat SARS-CoV-2 infection. The Authors. Published by Elsevier Inc. 2020-10 2020-07-07 /pmc/articles/PMC7341953/ /pubmed/32718560 http://dx.doi.org/10.1053/j.seminoncol.2020.07.002 Text en © 2020 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Oronsky, Bryan.
Knox, Susan.
Cabrales, Pedro.
Oronsky, Arnold.
Reid, Tony R.
Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19
title Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19
title_full Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19
title_fullStr Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19
title_full_unstemmed Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19
title_short Desperate Times, Desperate Measures: The Case for RRx-001 in the Treatment of COVID-19
title_sort desperate times, desperate measures: the case for rrx-001 in the treatment of covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7341953/
https://www.ncbi.nlm.nih.gov/pubmed/32718560
http://dx.doi.org/10.1053/j.seminoncol.2020.07.002
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