Canadian nod for Sobi's drug in rare genetic disorder

4 January 2017

Swedish Orphan Biovitrum (STO: SOBI) has received approval from Health Canada for its Orfadin (nitisinone) capsules for hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine.

HT-1 is a progressive, rare genetic disease that may result in liver and kidney complications and in most cases fatal if untreated. In the most common form of the disease, symptoms arise within the first six months of the child's life.

"This is an exciting moment for Sobi"

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