Article: Other News To Note.

o Abbott, of Abbott Park, Ill, said the European Medicine Agency's Committee for Medicinal Products for Human Use has recommended approval of Humira (adalimumab) for the treatment of severe Crohn's disease. Marketing approval is expected within 60 days. The company also said the FDA has given Humira priority review status for the treatment of moderately to severely active Crohn's disease. Humira is a fully human monoclonal antibody already approved for the treatment of rheumatoid arthritis, psoriatic arthritis and ankylosing spondylitis in the U.S. and Europe.

o Acacia Research Corp., of Newport Beach, Calif., said its CombiMatrix Corp., of Mukilteo, Wash., has ...

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