[Waking Times]:In 2003, severe acute respiratory syndrome (SARS) induced a global panic—a dress rehearsal, as it were, for Covid-19 in 2020. Although SARS fatalities rapidly petered out (with an eventual worldwide tally of just 774 deaths), concerns about the potential for future spread of the SARS coronavirus (SARS-CoV) left doctors eager to identify effective drugs for treatment and prevention.
In short order, researchers in Europe (2003 and 2004) and at the Special Pathogens Branch of the CDC (2005) published theoretical models and detailed in vitro findings about a drug offering likely “prophylactic and therapeutic advantage”: chloroquine (CQ).
Following these promising cell culture studies (cited hundreds of times in the scientific literature), researchers around the world continued to explore the antiviral potential of CQ and its more benign analog hydroxychloroquine (HCQ).
A 2006 paper in The Lancet Infectious Diseases again directed attention to CQ as a “valuable therapeutic option if SARS re-emerges.” In 2014, in the aftermath of the Middle East respiratory syndrome coronavirus (MERS-CoV), researchers at the Anthony Fauci led National Institute of Allergy and Infectious Diseases (NIAID) identified 27 existing compounds “with activity against both MERS-CoV and SARS-CoV,” including CQ and HCQ. Noting that the “screening of approved drugs to identify therapeutics for drug repurposing is a valid approach,” the NIAID researchers singled out CQ and one other drug in their closing paragraph as having noteworthy potential to “reconfigure” the two coronavirus illnesses “into a less virulent subclinical infection” resulting in less adverse disease outcomes....<<<Read The Full Article Here>>>...
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