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Recombinant human mutant tissue-type plasminogen activator (rhM-tPA) is an investigational thrombolytic biologic developed by Beijing World Trade Dongrui Pharmaceutical Technology. It is a genetically modified version of the endogenous human tissue-type plasminogen activator (tPA), a serine protease responsible for converting plasminogen into plasmin to dissolve fibrin-based blood clots. rhM-tPA is engineered to allow for administration as a single intravenous bolus, which may provide a clinical advantage over the standard-of-care alteplase (rt-PA) that typically requires an initial bolus followed by a continuous infusion. The drug is primarily being developed for the treatment of acute ST-segment elevation myocardial infarction (STEMI) and has been evaluated in Phase II clinical trials to compare its efficacy and safety against alteplase.
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