Press Release
Oral Laquinimod for Multiple Sclerosis Granted Fast Track Status by FDA Jerusalem, Israel and Lund, Sweden, February 12, 2009 - Teva Pharmaceutical Industries Ltd. (NASDAQ: TEVA) and Active Biotech (NASDAQ OMX NORDIC: ACTI) today announced that oral laquinimod, an investigational treatment for relapsing-remitting multiple sclerosis (RRMS), has received a Fast Track designation from the U.S. Food and Drug Administration (FDA).
Teva completed enrollment for the first of its two Phase III clinical trials for
laquinimod (ALLEGRO) in November 2008 and is currently enrolling RRMS patients globally for the second Phase III study (BRAVO).
to read the full report please go to
http://www.tevapharm.com/pr/2009/pr_823.asp
I wonder what the cost of a daily pill will be? Can't be the same as injectables, can it? It is so far just for those with RRMS.