Pink Sheet — FDA Panel To Consider Strategies For Timely Completion Of Accelerated Approval Confirmatory Trials
A US Food and Drug Administration advisory committee review of two Acrotech Biopharma LLC accelerated approval drugs with long-overdue confirmatory trial requirements may provide the clearest insight yet into how the Oncology Center of Excellence interprets the “due diligence” requirement for such studies and how sponsors’ planning and implementation strategies may factor into this determination. The Oncologic…