Lepu -Model NeoVas -Sirolimus-Eluting Bioresorbable Coronary Scaffold System

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Stent Platform: Fully degradable poly(L-lactide). Sine wave structure in space, In-phase peak-valley connection.

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Drug coating

  • Fully degradable poly(D,L-lactide)
  • Effectively control sirolimus release rate

Drug

  • Classical Sirolimus with dose of 15.3ug/mm
  • Inhibit the proliferation and migration of smooth muscle cells

Delivery system

  • Completely self-developed second-generation rapid-exchange balloon dilatation catheter
  • Superior pushability and crossability

NeoVas RCT Study

The study enrolled 560 subjects in 33 centers from China, Test group(NeoVas): 278 cases, Control group (Xience stent): 282 cases.

Conclusion:

The clinical events rate for Neovas bioabsorbable stent is low, showed equal safety and effectiveness with Xience metal stent.

NeoVas OPC study

The study enrolled 1103 subjects in 45 centers from China, two year clinical follow-up study has been completed to date.