National Sales Training Meetings - thoughts?????





We shouldn't get our hopes up that Incresync will get approved. No way will FDA approve it, TZD class doesn't meet the safety criteria of the FDA.

If Actos and the new DPPIVi used bioequivalent studies to get the combination approved, how can the FDA not approve Incresync based on the Pioglitazone portion of the drug without removing Actos from the market?
 




If Actos and the new DPPIVi used bioequivalent studies to get the combination approved, how can the FDA not approve Incresync based on the Pioglitazone portion of the drug without removing Actos from the market?

Ask Novartis why their gout drug wasn't approved. It wasn't better than current therapeutic options. How will this combination drug be better and more cost effective than the current line up of DPP4's and generic Actos?