Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 I'm still exhausted from my PCP appointment, so I have not been on top of my inbox, but I had to forward this. Cephalon has applied for FDA approval of Fentora (patented fentanyl immediate release product) for non-cancer BTP (Breakthrough Pain), which means that (if it is approved) insurance companies could no longer deny non-cancer patients access to Fentora simply for the fact that they do not have a cancer diagnosis!!! I believe that this is a response to the new REMS program (old REMS programs did not cover Fentora, Actiq, or generics). Cephalon manufacturers Fentora, Actiq, and all but two of the generic OTFC (generic Actiq). FDA approval can take 10-12 months and the press release is dated November 12, 2011, so it could be approved by the end of the year! Once approved, more doctors will likely be educated on it and prescribe it more and then the price will likely go down and then more insurance companies will cover it. I know, I know, I should not hold my breath but I need to convince myself it will happen. Fentora may taste like crap, but if it helps half as much as Actiq, or is beyond worth it. Cephalon Submits Supplemental New Drug Application for FENTORA bit'.'ly/MCMYnL Link is case sensitive, just replace '.' with . and the link should work fine. If you have trouble with the link, please email me off board (some messages boards do not permit clickable links) Steve M in PA Quote Link to comment Share on other sites More sharing options...
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