23 November 2020

Regeneron Pharmaceuticals has announced that its antibody cocktail casirivimab and imdevimab, also known as REGN-COV2 or REGEN-COV2, has received emergency use authorisation (EUA) from the US Food and Drug Administration (FDA). The drugs can be used for treating adults suffering with mild to moderate Covid-19 symptoms and  children aged 12 years or over weighing 40kg or more who are at risk of developing severe symptoms.

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Health Canada granted interim authorisation for the use of Eli Lily’s neutralising antibody bamlanivimab (LY-CoV555) for the treatment for adults and children aged 12 years and older who may be suffering from mild to moderate Covid-19 symptoms. The authorisation is based on data from the BLAZE-1 trial, a randomised, double-blind placebo-controlled Phase II study which showed reduced viral load and symptom as well as hospitalisation rates.

Pfizer and BioNTech announced that the companies will be submitting a request for emergency use authorisation (EUA) to the FDA for their mRNA vaccine candidate, BNT162b2 to fight against the SARS-CoV-2 virus. This will enable the provision of the vaccine among high-risk populations in the US by end of December 2020.

The Dow University of Health Sciences in Pakistan published positive results from the clinical trials of Covid-19 intravenous immunoglobulin (C-IVIG). The medical institute announced that C-IVIG showed 100% recovery rate among severe patients, and over 60% recovery in critical patients, and with more than 50% recovered and discharged within five days.

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