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Remicade.

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| February 15, 2001 | Mechcatie, Elizabeth | COPYRIGHT 2001 International Medical News Group. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

(infliximab, Centocor)

A tumor necrosis factor-[alpha] (TNF-[alpha]) blocker to inhibit progression of joint damage when used with methotrexate, in people with moderately to severely active rheumatoid arthritis with inadequate response to methotrexate. This is a newly approved claim; approved in 1999 for treating rheumatoid arthritis after inadequate response to methotrexate.

* Dosage: Intravenous infusions usually administered 2 and 6 weeks after an initial infusion, followed by an infusion every 8 weeks.

* Special Considerations: Serious infections, including sepsis and fatal infections have been reported in people on Remicade and Enbrel (etanercept), the other TNF blocker on the market.

* Comment: Approval of the new claim was based on results of a multicenter study of 428 predominantly white women with moderate to severe RA with active disease despite methotrexate treatment. Over 1 year, patients on Remicade and methotrexate had sustained reductions in RA signs and symptoms that significantly exceeded ...

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Source: HighBeam Research, Remicade.

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