IDIX – Sebivo (Telbivudine) for HBV has been submitted to regulatory authorities as follows: FDA: Dec 2005 (<a href='read_msg.asp?message_id=9102924'>#msg-9102924</a>) EU: Feb 2006 (<a href='read_msg.asp?message_id=9597987'>#msg-9597987</a>) China: Mar 2006 (<a href='read_msg.asp?message_id=10366668'>#msg-10366668</a>) Action dates are Oct 2006 for the FDA and early 2007 for the EU and China.