Remicade for children with Crohn’s Disease

The FDA's priority review program has lived up to its name, as only a month since being accepted into that program the Food and Drug Administration has approved the use of Remicade (Infliximab) for children with Crohn's Disease. The trial they examined showed that the medicine was as effective in children as in adults, and that it had the same side-effects.

Remicade is a genetically engineered monoclonal antibody, which reduces inflammation (swelling/redness) by blocking the action of tumor necrosis factor-alpha (TNF-α), that was initially approved in 1998 to treat Crohn's disease in adults.
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The safety and effectiveness of Remicade in pediatric Crohn's disease were assessed in a randomized study in 112 children who were 6 to 17 years old with moderately to severely active Crohn's disease who had an inadequate response to conventional therapies. The proportion of these patients who achieved clinical response compared favorably with the proportion of adults in an earlier Remicade study in adult Crohn's disease, and the pediatric trial's results showed no new safety concerns not already expressed in the product's current label.

In other news relating to Remicade and its sibling Humira, the Washington Post notes that serious side-effects have recently been reported in adults:

Approval comes after Wednesday's publication in the Journal of the American Medical Association of a study in which researchers said they found an apparent link between Remicade and a second drug, Humira, and some types of cancer in rheumatoid arthritis patients. Those cancers include skin, gastrointestinal, breast and lung tumors.

The FDA-approved labeling for Remicade, also called infliximab, already mentions the drug's association with an increased risk of lymphoma and other cancers, including skin, breast and colorectal, the regulatory agency and the drug's manufacturer both said. The label also mentions an increased risk of serious and sometimes fatal infections, as well as disorders of the blood and central nervous system.

Update 23-May-2006: Abbott, the manufacturer of Humira, has responded:

The conclusion in the JAMA article regarding risk of infection in those taking anti-TNF agents restates what has already been observed in the clinical trials of all three anti-TNFs. These data have been reviewed in a U.S. Food and Drug Administration (FDA) Arthritis Advisory Committee meeting in March 2003, and routinely since that time. The information in the JAMA article on infections is well documented in the labeling of all three anti-TNF agents, including HUMIRA (adalimumab).

Abbott disagrees with the authors' conclusions that their analysis establishes an increased risk of malignancies attributable to the anti-TNF agents included in their meta-analysis. The potential role, if any, of TNF-blocking therapy in the development of malignancies is not known, and this is reflected in the labeling of all three agents.