Nabumetone's position as one of the most commonly used nonsteroidal antiinf
lammatory drugs (NSAIDs) in the world today is based upon over a decade of
clinical experience. The popularity of this drug lies in both its unique ph
armacokinetic profile and special safety features in pharmacodynamic terms.
This nonacidic prodrug with an active 6-methoxy-2-naphthylacetic acid (6-M
NA) metabolite has COX-2 preferential features and is also devoid of entero
hepatic recirculation. It is felt that these characteristics have provided
the basis for its unique long term tolerability, documented in various at-r
isk osteoarthritis and rheumatoid arthritis populations. The excellent tole
rability of nabumetone and its 24-hour half-life, which provides the advant
ages of a once-daily dosage regimen, make it uniquely suitable for long ter
m anti-inflammatory therapy in arthritis.
The tolerability profile of nabumetone has also demonstrated clear cost-eff
ectiveness advantages, as confirmed by comparative and epidemiological stud
ies. Selective COX-2 NSAIDs are likely to prove more expensive because of t
he increasing costs and demands of clinical research prior to FDA approval.
These higher costs may limit and influence patient access, depending on th
e healthcare delivery system, and many years of experience will be required
to document the putative tolerability advantages of these newer COX-2 inhi
bitor agents. In the meantime, it is comforting that nabumetone has establi
shed such an advantageous tolerability profile together with acknowledged e
fficacy.