MNTA: Teva’s phase-3 trial of the 40mg dose of Copaxone in MS failed to show any benefit vs the standard 20mg dose: <a href="http://www.reuters.com/article/marketsNews/idINBNG13619120080707" target="_blank">http://www.reuters.com/article/marketsNews/idINBNG13619120080707</a> This is modestly good news for MNTA in that Teva’s US patents on the 40mg dose might have harder to overturn or circumvent than the patents on the standard 20mg dose. (MNTA is developing a generic version of Copaxone with its partner, NVS.) <!--Beg_Sig--> <a href=http://www.investorshub.com/boards/board.asp?board_id=1418>Let’s talk biotech!</a> What if there were no hypothetical questions?