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-- Reducing signs and symptoms, inhibiting the progression of structural
damage and improving physical function in patients with moderately to
severely active RA, when administered in combination with methotrexate.
-- Reducing signs and symptoms in patients with active AS.
-- Reducing signs and symptoms and inducing and maintaining clinical
remission in adult and pediatric patients with moderately to severely
active CD who have had an inadequate response to conventional therapy.
-- Reducing the number of draining enterocutaneous and rectovaginal
fistulas and maintaining fistula closure in adult patients with
fistulizing CD.
-- Reducing signs and symptoms, inducing and maintaining clinical
remission and mucosal healing, and eliminating corticosteroid use in
patients with moderately to severely active UC who have had an
inadequate response to conventional therapy.
-- Reducing signs and symptoms of active arthritis, inhibiting the
progression of structural damage and improving physical function in
patients with PsA.
-- Treatment of adult patients with chronic severe plaque PsO who are
candidates for systemic therapy and when other systemic therapies are
medically less appropriate.
REMICADE is unique among available anti-TNF biologic therapies. Unlike self-administered therapies that require patients to inject themselves frequently, REMICADE is the only anti-TNF biologic administered directly by caregivers in the clinic or office setting. REMICADE is a two-hour infusion administered every 6 or 8 weeks (indication-dependent), following a standard induction regimen that requires treatment at weeks 0, 2 and 6. As a result, REMICADE patients may require as few as six treatments each year.
Important Safety Information
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