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INTERCEPT Blood System for RBCs Study in Regions at Potential Risk for Zika Virus Transfusion-Transmitted Infections

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NCT03037164

Sponsored by Cerus Corporation (industry) · CERS — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
692actual
Sites
16
Countries
Puerto Rico, Turkey (Türkiye), United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2017-05-11actualWhen the study began enrolling
Primary completion2026-07-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-12-30estimatedThe whole study's end, after follow-up
First posted2017-01-31estimatedWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Anemia

Interventions

  • Device: INTERCEPT Blood System for Red Blood Cells
  • Device: Conventional (Control)

Primary outcomes

what the primary-completion date above is the date OF
Adjusted hemoglobin increment
measured 15 minutes - 24 hours post transfusion
Adverse Events
measured 28 days
Treatment emergent antibodies
measured 75 days

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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