Author: Rosenke, Kyle; Jarvis, Michael A.; Feldmann, Friederike; Schwarz, Benjamin; Okumura, Atsushi; Lovaglio, Jamie; Saturday, Greg; Hanley, Patrick W.; Meade-White, Kimberly; Williamson, Brandi N.; Hansen, Frederick; Perez-Perez, Lizette; Leventhal, Shanna; Tang-Huau, Tsing-Lee; Nason, Martha; Callison, Julie; Haddock, Elaine; Scott, Dana; Sewell, Graham; Bosio, Catharine M.; Hawman, David; de Wit, Emmie; Feldmann, Heinz
Title: Hydroxychloroquine Proves Ineffective in Hamsters and Macaques Infected with SARS-CoV-2 Cord-id: y5cbp2yz Document date: 2020_6_11
ID: y5cbp2yz
Snippet: We remain largely without effective prophylactic/therapeutic interventions for COVID-19. Although many human clinical trials are ongoing, there remains a deficiency of supportive preclinical drug efficacy studies. Here we assessed the prophylactic/therapeutic efficacy of hydroxychloroquine (HCQ), a drug of interest for COVID-19 management, in two animal models. When used for prophylaxis or treatment neither the standard human malaria dose (6.5 mg/kg) nor a high dose (50 mg/kg) of HCQ had any ben
Document: We remain largely without effective prophylactic/therapeutic interventions for COVID-19. Although many human clinical trials are ongoing, there remains a deficiency of supportive preclinical drug efficacy studies. Here we assessed the prophylactic/therapeutic efficacy of hydroxychloroquine (HCQ), a drug of interest for COVID-19 management, in two animal models. When used for prophylaxis or treatment neither the standard human malaria dose (6.5 mg/kg) nor a high dose (50 mg/kg) of HCQ had any beneficial effect on clinical disease or SARS-CoV-2 kinetics (replication/shedding) in the Syrian hamster disease model. Similarly, HCQ prophylaxis/treatment (6.5 mg/kg) did not significantly benefit clinical outcome nor reduce SARS-CoV-2 replication/shedding in the upper and lower respiratory tract in the rhesus macaque disease model. In conclusion, our preclinical animal studies do not support the use of HCQ in prophylaxis/treatment of COVID-19.
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