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Blood safety stories

Nov 2, 2026

Cerus blood-safety system meets primary endpoint in late-stage trial

Cerus Corp announced that red blood cells treated with its blood-safety technology performed as well as conventional red blood cells in patients requiring transfusions in a late-stage study.

Nov 2, 2026·2 sources
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Top claims

  • ▪Cerus Corporation's Phase 3 RedeS trial showed no statistically significant difference in treatment-emergent adverse events between the INTERCEPT arm and the control arm (p=0.634)
  • ▪The INTERCEPT Blood System for Red Blood Cells remains investigational in the United States and has not been approved by the FDA
  • ▪The INTERCEPT Blood System for Red Blood Cells is under regulatory review in Europe

Subtopics

Biotech innovation1Clinical trial endpoints1Clinical trials1Drug Policy, Pricing & Approval1FDA regulatory approval1Hematology1

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