The CHMP adopted a positive re-examination opinion for Aubagio, revising its previous opinion not to grant new active substance status to the medicine at its March 2013 meeting.
Thus, Aubagio is now entitled to the standard “8+2+1” EU exclusivity afforded to new drugs.
As previously noted (#msg-86099393), Aubagio has five years of US exclusivity conferred by FDA NCE status despite the fact that it’s almost indistinguishable from a prior approved drug (Aravo) in vivo.
*New Active Substance (equivalent to NCE status in US terminology).
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”