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* Note: The information below is only for reference by medical professionals.

Thrombolysis patency rate of 83%

Phase II Clinical Study of Mineflex Heart Attack

Study design: a randomized, blinded, parallel, positive-controlled, multicenter clinical study enrolling 251 patients aged 18-70 years with STEMI within 12 h of onset

Primary efficacy: The patency rate of Reflow™ (rhTNK-tPA) 16 mg for 90 min infarcted blood vessels was significantly higher than that of recombinant human tissue-type plasminogen activator (rt-PA) (p<0.05)

Phase IV clinical study of Mefloquine infarction

Study design: a randomized, open, parallel, positive-controlled, non-inferiority trial enrolling 823 patients at 115 participating centers

The primary endpoint showed that the incidence of MACCE at 30 days was similar or even slightly lower for mefloquine compared to alteplase.

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Phase IV clinical study of Mefloquine infarction

The safety results show that the risk of bleeding is low and the safety profile of Mafenox is not comparable to that of rt-PA.

Real-world research after the listing of Mineflex

Study design: a combined prospective and retrospective, open-ended, single-group, multicenter IDM design with 1010 active cases enrolled.

The results showed that gingival bleeding (3.9%) was the most common adverse event, while other bleeding events were occasional (≤1%), the incidence of death (3.9%) and cerebral hemorrhage (0.3%) were not above the lower limit of the epidemiological study level, and no new serious risk signals were found for MDFL.

The premium thrombolytic drug recommended by domestic and international guidelines

*Reflow (rhTNK-tPA) is the only Tenecteplase currently marketed in China

*Prescription drugs should be used under the guidance of professional physicians. For product details, refer to the Package Insert.