Teva Pharmaceutical Industries Ltd. intends to respond to FDA’s complete response letter for deutetrabenazine for the treatment of chorea associated with Huntington disease by the end of September, which could position the drug for approval and launch in March 2017, President Global R&D Michael Hayden said during the company’s second quarter conference call Aug. 4.
Teva is working to quickly resolve the outstanding issues because deutetrabenazine (also known as SD-809) is expected to be an important future growth driver for the company’s specialty business. The...
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