Alexion Biologic Soliris Is First To Get FDA Nod For Rare Blood Disease
This article was originally published in The Pink Sheet Daily
Soliris is slated to launch within two weeks from its March 16 approval.
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The devastating natural course of atypical hemolytic uremic syndrome, coupled with the small quantity of drug used to treat pediatric patients, means the new use is expected to have only a small impact on sales initially, Alexion's management says.