Thrombolysis is now standard therapy for the treatment of acute myocardial infarction. However, evidence suggests that earlier treatment and more rapid and complete recanalization of infarct-related coronary arteries may lead to greater survival benefits than achieved by current therapies. Furthermore, first-and second-generation thrombolytics can be associated with side effects, such as bleeding complications, and often require prolonged infusion or complex dosing regimens to optimize clinical outcome. Reteplase, a novel recombinant plasminogen activator (thrombolytic), is a deletion variant of native, human t-P A that has been designed to provide a longer half-life plus more specific and rapid lysis of coronary thrombi, using a bolus dosing regimen. Clinical studies comparing reteplase with the current standard thrombolytic agents have demonstrated that reteplase has a highly favourable pharmacological profile with prolonged half-life, low bleeding risk and low potential for antigenicity.
CITATION STYLE
Waller, M., & Kohnert, U. (1999). Reteplase, a recombinant plasminogen activator. In Biopharmaceuticals, an Industrial Perspective (pp. 185–216). Springer Netherlands. https://doi.org/10.1007/978-94-017-0926-2_8
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