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NCT06697223

A Study to Assess Recovery and Survival of Radiolabeled Apheresis Platelet Components Treated With the INTERCEPT Blood System for Platelets With LED Illuminator.

Completed Phase 2 Last updated 6 February 2026
What this trial tests

Phase 2 trial testing INTERCEPT Blood System for Platelets with LED Illuminator in Healthy Subjects in 40 participants. Completed in 13 June 2025.

Timeline
23 January 2025
Primary endpoint
2 June 2025
13 June 2025

Quick facts

Lead sponsorCerus Corporation
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment40
Start date23 January 2025
Primary completion2 June 2025
Estimated completion13 June 2025
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Cerus Corporation — full company profile →

Who can join

18 and older, any sex, with Healthy Subjects. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to assess the post-infusion recovery and survival of platelets in 100% Plasma treated with INTERCEPT Blood System for Platelets with LED Illuminator and stored for 5 days after apheresis collection. The post-infusion recovery and survival of autologous radiolabeled 5-day INTERCEPT platelets (Test) stored in 100% plasma will be measured in comparison to fresh autologous radiolabeled platelets (Control).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Healthy Subjects

Currently open trials in the same condition.

Other Cerus Corporation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06697223.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing