The University of Minnesota’s Center for Infectious Disease Research & Policy (CIDRAP) has reported that AstraZeneca‘s monoclonal antibody combination drug, Evusheld, failed to improve outcomes in a Phase III trial involving hospitalised Covid-19 patients.
Evusheld was given to 214 of the 399 participants in the DISCOVERY study and did not offer substantial improvement in clinical status or expedite viral clearance in these patients.
Go deeper with GlobalData
Despite this, the drug was found to cause a substantial increase in neutralising antibodies against SARS-CoV-2 at days three and eight.
Although no major safety events or increased cardiovascular risks were recorded, the trial found no significant differences in mortality or hospital admission rates between those who received Evusheld and those given standard care.
The mortality rate at day 90 was around 15% for both the control arm and the cases.
See Also:
Researchers speculate that different Covid-19 variants present in the trials could have caused the discrepancy between the results of the DISCOVERY trial and the prior ACTIV-3-TICO study, which showed a decline in mortality at day 15.
How well do you really know your competitors?
Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.
Thank you!
Your download email will arrive shortly
Not ready to buy yet? Download a free sample
We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form
By GlobalDataIn the DISCOVERY trial, 40% of infections were caused by the Omicron variant, whereas the ACTIV trial occurred primarily during the prevalence of the Delta variant.
The Omicron variant’s ability to evade Covid-19 vaccines and therapeutic monoclonal antibodies (mABs) has been noted as more pronounced than that of the original strain or Delta variant.
Evusheld is a combination of two long-acting antibodies, tixagevimab (AZD8895) and cilgavimab (AZD1061).
These antibodies were discovered by the Vanderbilt University Medical Center and were licensed to AstraZeneca in 2020.
AstraZeneca reported in June 2022 that detailed data from the Phase III TACKLE trial indicated that Evusheld provided clinically and statistically significant protection against progression to severe Covid-19 or mortality from any cause compared to a placebo.
The outpatient setting findings also suggested that early-stage Covid-19 treatment with Evusheld could lead to more favourable outcomes.
