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U.S. FDA approves first biosimilar rival to Roche’s blockbuster eye drug – Metro US

U.S. FDA approves first biosimilar rival to Roche’s blockbuster eye drug

FILE PHOTO: Signage is seen outside of FDA headquarters in
FILE PHOTO: Signage is seen outside of FDA headquarters in White Oak, Maryland

(Reuters) – The U.S. Food and Drug Administration on Monday approved South Korean drugmaker Samsung Bioepis Co Ltd and Biogen Inc’s biosimilar rival to Roche Holding AG’s blockbuster eye drug, Lucentis.

Biosimilars are cheaper versions of biologic drugs made from living organisms.

Lucentis, which already faces competition from Novartis AG’s Beovu, is approved to treat eye diseases such as wet age-related macular degeneration and brought in sales of CHF 1.4 billion ($1.50 billion) in 2020.

The copycat version will be allowed to be marketed in the United States from next year June, as part of an agreement with Roche’s Genentech unit, the drug developers said in a joint statement.

($1 = 0.9304 Swiss francs)

(Reporting by Manas Mishra in Bengaluru; Editing by Shinjini Ganguli)