VRTX to begin a new phase III study (REALIZE) of telaprevir in HCV treatment failures (it will enroll null responders, partial responders and relapsers). Telaprevir dose - 750mg, q8h, for 12 weeks + 36 weeks. <a href="http://investors.vrtx.com/releasedetail.cfm?ReleaseID=328603" target="_blank">http://investors.vrtx.com/releasedetail.cfm?ReleaseID=328603</a>