emergency use authorisation

Britain approved the vaccine for emergency use less than a week ago, and is rolling it out through its National Health Service…

No date has been fixed as on when the SEC will meet for assessing and evaluating the applications, as per sources

According to sources, this vaccine is logistically feasible for distribution in the country's both urban and rural parts as it can…

It is the first company to seek approval for its vaccine in India

The company claims that approximately 2000 COVID-19 patients used the drug under the emergency use authorisation

Care home residents, health and care staff, the elderly and people who are clinically extremely vulnerable will be first in line

Primary efficacy analysis of the Phase 3 COVE study of mRNA-1273 involving 30,000 participants included 196 cases of COVID-19, of…

In a clinical trial, casirivimab and imdevimab, administered together, were shown to reduce COVID-19-related hospitalisation or…

Baricitinib is an FDA-approved drug to treat rheumatoid arthritis

It will seek emergency use authorisation from the US Food and Drug Administration once it has more safety data, expected later…