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Clinical Trial Summary

The clinical study will assess the in-vitro characteristics of red blood cells (RBCs) per the European Union (EU) criteria for leukocyte depleted RBCs in additive solution and evaluate the safety and efficacy of S-303 treated RBCs in a patient population requiring RBC transfusion support for acute anemia.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator)


Related Conditions & MeSH terms

  • Anemia
  • Focus:Use of S303 RBCs in Patients With Acute Anemia

NCT number NCT01716923
Study type Interventional
Source Cerus Corporation
Contact
Status Completed
Phase Phase 3
Start date April 2013
Completion date October 2014