LONDON (Reuters): An international trial testing convalescent blood plasma on COVID-19 patients with moderate and severe illness has halted enrolment of severely ill COVID-19 patients requiring intensive care after it found no benefit, trial investigators said on Monday.
“There was no evidence of harm associated with the administration of convalescent plasma” (and) the trial is continuing to recruit hospitalised COVID-19 patients who are moderately ill but not in intensive care, scientists leading the trial said in a statement.
“It is biologically plausible that patients who are not producing antibodies at the time of convalescent plasma therapy and those patients with excess virus may benefit more than others. Our additional analyses will explore this,” said Manu Shankar-Hari, a clinician and professor of critical care medicine at Britain’s Guy’s and St Thomas’ hospital, who is co-leading the trial.
He added that the initial analysis did not assess plasma’s effects in hospitalised patients with less severe disease. This “remains a very important question” and would continue to be explored in the ongoing trial, he said.
The underlying hypothesis for using convalescent plasma as a potential treatment for COVID-19 patients is that the antibodies it contains could neutralize the virus, stopping it from replicating and halting tissue damage.
But this initial analysis leading to the REMAP-CAP pause in enrolment of critically ill patients showed there was a very low probability – 2.2 percent – that it reduced death rates or decreased the number of days patients needed intensive care.
“Why convalescent plasma does not seem to improve outcome in severely ill COVID-19 patients admitted to the ICU is not yet known. However, it may be because the lung damage is too advanced for convalescent plasma to make a difference,” said Alexis Turgeon, a critical care doctor and professor at Université Laval in Canada, who is also working on the trial.
REMAP-CAP is an international clinical trial exploring potential treatments for COVID-19. It has already recruited 4,100 COVID-19 patients at more than 290 clinical sites across Europe, the Americas, Asia, Africa and Australasia.
Separate findings from REMAP-CAP showed last week that treating critically ill COVID-19 patients with Roche’s Actemra or Sanofi’s Kevzara arthritis drugs significantly improved survival rates and reduced the amount of time patients need intensive care.
The trial is also looking at potential effects of a range of other existing therapies, including anticoagulation medicines, antiplatelet agents, antibiotics, statins and vitamin C.