Celebrex: Drug in Same Class as Recalled Vioxx

On December 17, 2004 The Food and Drug Administration (FDA) learned from the National Cancer Institute (NCI) and Pfizer, Inc., that NCI stopped drug administration in an ongoing clinical trial investigating a new use of Celebrex (celecoxib) to prevent colon polyps because of an increased risk of cardiovascular (CV) events in patients taking Celebrex versus those taking a placebo.

Patients in the clinical trial taking 400 mg. of Celebrex twice daily had a 3.4 times greater risk of CV events compared to placebo. For patients in the trial taking 200 mg. of Celebrex twice daily, the risk was 2.5 times greater. The average duration of treatment in the trial was 33 months.

A similar ongoing study comparing Celebrex 400 mg. once a day versus placebo, in patients followed for a similar period of time, has not shown increased risk.

Though these findings are important the FDA has seen only the preliminary results of the studies. The FDA reports it will obtain all available data on these and other ongoing Celebrex trials as soon as possible and will determine the appropriate regulatory action.

Although the FDA has not seen not seen all available data on Celebrex, the findings are similar to recent results from a study of Vioxx (rofecoxib), another drug in the same class as Celebrex. Vioxx was recently voluntarily withdrawn by Merck.

Another drug in this class, Bextra (valdecoxib) has shown an increased risk for CV events in patients after heart surgery. Bextra and Celebrex are the only two selective COX-2 agents currently on the U.S. market.

According to the FDA, physicians should consider this evolving information in evaluating the risks and benefits of Celebrex in individual patients. FDA advises evaluating alternative therapy. At this time, if physicians determine that continued use is appropriate for individual patients, FDA advises the use of the lowest effective dose of Celebrex.

Patients who are currently taking Celebrex and have questions or concerns about the drug should discuss them with their physicians.

Celebrex was approved in 1998 for the treatment of osteoarthritis and rheumatoid arthritis. Previous large studies of Celebrex, including clinical trials and epidemiology studies, have not suggested the sort of CV risk found in the NCI polyp study. Because similar long-term studies of other products in the class of non-steroidal anti-inflammatory drugs (NSAIDS), other than Cox-2 inhibitors have not been done, it is not known whether other NSAIDS pose a similar risk.

Celebrex Information on the Web:

Study: Celebrex as Risky as Vioxx (4/15/05)

Pfizer Reveals Study linking Celebrex to Heart Risks
(Boston Globe, 2/1/05)

New England Journal of Medicine Recommends Not Prescribing Celebrex (12/23/04)

FDA Urges Alternatives to Celebrex: Pfizer Finds Increased
Heart Risk with Pain Reliever (Associated Press, 12/18/04)

© 2008 Fonvielle Lewis Foote & Messer