Absent quality data, the use of these drugs in management of COVID-19 should be reserved for clinical trials.
The COVID-19 pandemic is challenging the slow and highly regulated drug-approval process in the United States. On March 28, 2020, the U.S. FDA authorized use of the antimalarial drugs chloroquine (CQ) and hydroxychloroquine (HCQ) to treat COVID-19 patients for whom a clinical trial is not available, despite inconclusive clinical evidence of effectiveness.
What sparked interest in these drugs? Most COVID-19 patients probably are in an antiviral-susceptible stage before clinical presentation. Following a primary phase marked by the usual respiratory symptoms, fevers, and malaise, patients most affected by COVID-19 develop a severe inflammatory respiratory illness, driven largely by the host immune response. Laboratory data show evidence of mas…
Authors
DisclosuresConsultant/Advisory BoardParatek Pharmaceuticals; Nestle Corp.; AbbVie; Shionogi
Speaker’s BureauAllergan/AbbVie; Paratek Pharmaceuticals; Nestle Corp.
RoyaltiesUpToDate
Editorial BoardsAntimicrobial Agents and Chemotherapy; Open Forum Infectious Diseases
DisclosuresConsultant/Advisory BoardParatek Pharmaceuticals; Nestle Corp.; AbbVie; Shionogi
Speaker’s BureauAllergan/AbbVie; Paratek Pharmaceuticals; Nestle Corp.
RoyaltiesUpToDate
Editorial BoardsAntimicrobial Agents and Chemotherapy; Open Forum Infectious Diseases
DisclosuresGrant/Research SupportNational Institutes of Health
DisclosuresGrant/Research SupportNational Institutes of Health
DisclosuresConsult/Advisory BoardAcurx Pharmaceuticals, LLC;
Grant/Research SupportDoctors Company Foundation, Massachusetts Department of Public Health
DisclosuresConsult/Advisory BoardAcurx Pharmaceuticals, LLC;
Grant/Research SupportDoctors Company Foundation, Massachusetts Department of Public Health