Several third-generation thrombolytic agents have been developed. They are
either conjugates of plasminogen activators with monoclonal antibodies agai
nst fibrin, platelets, or thrombomodulin; mutants, variants, and hybrids of
alteplase and prourokinase (amediplase); or new molecules of animal (vampi
re bat) or bacterial (Staphylococcus aureus) origin. These variations may l
engthen the drug's half-life, increase resistance to plasma protease inhibi
tors, or cause more selective binding to fibrin. Compared with the second-g
eneration agent (alteplase), third-generation thrombolytic agents such as m
onteplase, tenecteplase, reteplase, lanoteplase, pamiteplase, and staphylok
inase result in a greater angiographic patency rate in patients with acute
myocardial infarction, although, thus far, mortality rates have been simila
r for those few drugs that have been studied in large-scale trials. Bleedin
g risk, however, may be greater. Am J Med. 2000;109:52-58. (C) 2000 by Exce
rpta Medica, Inc.