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SGEN — Seagen News Story

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FDA nod for Seagen's cancer combo therapy makes 'multi-blockbuster' - Analysts

** U.S. FDA late on Monday granted accelerated marketing
approval to Seagen Inc's  SGEN.O  Padcev and Merck & Co's
 MRK.N  blockbuster drug Keytruda as combination first-line
treatment of bladder cancer
    ** Brokerage firm William Blair said the approval expands
the reach of Padcev in a $2.5 bln-$3 bln global market for
bladder cancer 
    ** Padcev has already been approved as a monotherapy to
treat patients with bladder cancer by US FDA in 2021
    ** The combination therapy comes with a boxed warning for
serious skin reactions
    ** The approval is an inflection point for SGEN's revenue
growth trajectory, propelling Padcev to a multi-blockbuster
franchise - William Blair 
    ** Brokerage BMO capital forecast U.S. sales of $3.5 bln for
Padcev in 2030 
    ** As of last close, SGEN up ~57% YTD

 (Reporting by Khushi Mandowara in Bengaluru)
 ((Khushi.Mandowara@thomsonreuters.com;))

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