Guest guest Posted October 1, 2000 Report Share Posted October 1, 2000 Hi Here is some information on 2 inhibitors I thought I would pass. Hope it helps. During the 1998 American College of Rheumatology Scientific Meetings, researchers presented information regarding Celebrex (celecoxib). The report concluded that Searle and Pfizer's investigational drug Celebrex relieved arthritis pain as well as full therapeutic doses of commonly prescribed non-steroidal anti-inflammatory (NSAID) pain relievers. Merck was also working on the development of a similar drug, Vioxx (rofecoxib). Celebrex and Vioxx both belong to a class of compounds called COX-2 inhibitors. COX is short for cyclo-oxygenase, an enzyme involved in the cascade of cellular events that eventually produce inflammation. As it turns out, there are two forms of the enzyme, COX-1 and COX-2. NSAIDs inhibit both enzymes, which is unfortunate, since COX-1 has another job. It produces prostaglandin a substance that's critical in the production of a type of mucus that lines and protects the stomach and intestines. It's the NSAIDs' inhibition of COX-1 that's the cause of their unpleasant gastrointestinal side effects, including heartburn, ulcers, and bleeding. COX-2 inhibitors leave COX-1 alone, thus decreasing gastrointestinal side effects while providing the same analgesic effects as NSAIDs. On December 31, 1998 the FDA approved Celebrex for relief of the signs and symptoms of osteoarthritis (OA) and adult rheumatoid arthritis (RA). Vioxx followed and received approval in May of 1999 for the treatment of osteoarthritis, menstrual pain and for the management of acute pain in adults. Quote Link to comment Share on other sites More sharing options...
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