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UCB’s Meeting With U.S. FDA Defines Path Forward For Cimzia(R) In Rheumatoid Arthritis. (Medical News Today)

UCB announced that it met the U.S. Food and Drug Administration (FDA) and clarified the requirements for the approval of the Biologics License Application (BLA) for Cimzia®, the first PEGylated anti-TNF, for the treatment of rheumatoid arthritis (RA). During the meeting, the FDA communicated that they require further analysis of existing data and a new safety update.

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