GILD’s GT3 issue, which the whole world seems willing to overlook, surfaces in this Bloomberg piece on the phase-2 study of Sofosbuvir + Daclatasvir in treatment-experienced patients:
Question Dew: Could failure to achieve GT3 labeling for Sofo/Riba, within the pooled data filing, delay approval for GT2 patients? Is it possible GILD would be required to refile the Sofo/Riba NDA for GT2?