The quest for an anti-restenotic drug continues to be a major challenge in
the field of cardiovascular pharmacology because most thera pies with prove
n efficacy in experimental neointima models have failed to limit restenosis
. Some drug classes, including glycoprotein IIb/IIIa antagonists, nitric ox
ide donors and the antioxidant probucol, have recently demonstrated potenti
al benefits in clinical trials. Progress in the development of local delive
ry systems for administration of drugs, antisense oligonucleotides or genes
, in combination with an improved understanding of the pathogenesis of rest
enosis holds promise for ultimate pharmacotherapy of this condition.