The Biocon stock was down 3.4 per cent after the US Food and Drug Administration (FDA) deferred its decision on the company’s application to launch a biosimilar of Bevacizumab in the American market. The market for the drug, which is used in treating some cancers and eye diseases, is pegged at $3 billion.
The US drug regulator was unable to inspect the company’s manufacturing facility because of travel restrictions on account of Covid-19. The application for approval was filed by Biocon’s subsidiary, Biocon Biologics.
While analysts have not modified their FY21 earnings estimates because of the delay in the approval process, they