Abbott Laboratories [1] says that the FDA will give its anti-inflammatory drug Humira [2] a priority review as a treatment for Crohn's disease. The priority review will move up a decision on Humira into early March, cutting four months off the timetable. To back up its application for Humira, Abbott submitted data from a trial of volunteers who had not responded to the monoclonal antibody Remicade [3] (infliximab) made by Centocor [4]. In Crohn's disease inflammation of the digestive tract causes pain and diarrhea. Humira has already been approved for rheumatoid arthritis and other conditions. Report [5]
Links:
[1] http://www.fiercebiotech.com/search/node/Abbott+Laboratories
[2] http://www.fiercebiotech.com/search/node/Humira+
[3] http://www.fiercebiotech.com/search/node/Remicade+
[4] http://www.fiercebiotech.com/search/node/Centocor
[5] http://www.chron.com/disp/story.mpl/ap/fn/4290344.html