Late-stage study of COVID-19 convalescent-plasma treatment with remdesivir starts
A late-stage trial testing the combination of Gilead Sciences’ remdesivir and a highly concentrated solution of antibodies that neutralize the COVID-19 virus has begun, the National Institutes of Health (NIH) said on Thursday.
Trial investigators believe that giving the antibody solution to COVID-19 patients at the onset of symptoms could heighten the natural antibody response to the virus, thereby reducing the risk of severe illness and death.
Emergent BioSolutions, Grifols S.A., CSL Behring and Takeda Pharmaceutical are collaborating to supply the antibody solution, NIH said.
The study, which is testing the antibody solution made up with convalescent plasma from recovered COVID-19 patients, is being conducted with hospitalized adults in the United States, Mexico and sixteen other countries.
The main goal of the trial will be to compare the health status of the patients receiving the combination treatment with those on remdesivir only, after a week.
For more news about the novel coronavirus click here.
What you need to know about Coronavirus.
For more information on COVID-19, call the DOH Hotline: (02) 86517800 local 1149/1150.
The Inquirer Foundation supports our healthcare frontliners and is still accepting cash donations to be deposited at Banco de Oro (BDO) current account #007960018860 or donate through PayMaya using this link.