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The identical phase III, randomized, double-blind trials ASCLEPIOS I and II were published in 2020 (44)
Hewlett Packard, United States) inserted into the portal vein, inferior vena cava and abdominal aorta at the level of the bifurcation at 15 min, 24 h or 48 h post-ligation

Drug Pathway: No FDA New Drug Approval The FDA drug approval system is based on the NDA (New Drug Application) process
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