James Hester 07:43, 12 December 2017 Indivior, the London-listed pharmaceuticals company, revealed its schizophrenia treatment had been accepted for review by the US Food and Drug Administration (FDA).
The FDA could decide on whether to approve Indivior´s RBP-7000 drug by July 2018.
Recent Phase III clinical trials of RBP-7000 indicated significant improvement for those suffering from acute schizophrenia.
Why Capital.com?
Simple and intuitive platform
No commission
Competitive spreads
“FDA acceptance of our RBP-7000 NDA is a significant milestone for Indivior as we expand our treatment portfolio to offer a meaningful therapeutic option to help address non-compliance with medication administration in the treatment of schizophrenia," said Christian Heidbreder, chief scientific officer of Indivior.
Indivior shares have gained 29% over the past year.