F. Breedveld, TENIDAP - A NOVEL CYTOKINE-MODULATING ANTIRHEUMATIC DRUG FOR THE TREATMENT OF RHEUMATOID-ARTHRITIS, Scandinavian journal of rheumatology, 1994, pp. 31-44
Tenidap is a novel, once-daily, cytokine modulating antirheumatic drug
indicated for the treatment of rheumatoid arthritis (RA). In vitro, t
enidap significantly inhibits the production of the pro-inflammatory c
ytokines, interleukin-l, interleukin-6 and tumour necrosis factor in h
uman cell lines, and inhibits cytokine-mediated processes such as cart
ilage degradation, bone resorption, metalloprotease synthesis, endothe
lial cell adhesion and monocyte differentiation. Tenidap also inhibits
cyclo-oxygenase. In RA patients, tenidap 120 mg/day is clinically equ
ivalent to the combination of disease-modifying antirheumatic agents p
lus non-steroidal anti-inflammatory drugs (NSAIDs) and significantly m
ore effective than NSAIDs. Tenidap also produces rapid, profound and s
ustained reductions in the serum levels of the acute phase proteins, C
-reactive protein and serum amyloid A, an effect suggestive of disease
modifying properties. In addition, tenidap reduces circulating levels
of IL-6 in RA patients. Tenidap is well tolerated.