CSL receives FDA drug approval

Company News

CSL Limited (ASX:CSL) has announced that the US FDA has approved IDELVION, CSL’s long-acting albumin fusion protein for the treatment of haemophilia B.
 
The company says IDELVION delivers high-level protection with up to a 14-day dosing in appropriate patients, providing excellent bleeding control.
 
The product will be added to CSL’s growing portfolio of bleeding disorder products.
 
Haemophilia B is a congenital bleeding disorder, affecting one in 25,000 male births.
 
CSL reported a net profit of $983.85 million at 31 December 2015. 

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