FDA approves component of treatment regimen for most common childhood cancer

FDA

30 June 2021 - Today, the U.S. FDA approved Rylaze (asparaginase erwinia chrysanthemi (recombinant)-rywn) as a component of a chemotherapy regimen to treat acute lymphoblastic leukaemia and lymphoblastic lymphoma in adult and paediatric patients who are allergic to the E. coli derived asparaginase products used most commonly for treatment. 

The only other FDA approved drug for such patients with allergic reactions has been in global shortage for years.

Read FDA press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Cancer , Outcome , Medicine