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?
HELLO!!!! Pioglitazone has been shown to cause some really bad shit in humans. Do you think any company wants to use it in a combo product? WTF?