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NCT07015437 · ClinicalTrials.gov registry record · Phase 2

A Recovery and Lifespan Study Using INTERCEPT Red Blood Cells Prepared Using the INTERCEPT Blood System for RBCs With AS-1

A Phase 2 study of Healthy Subjects, sponsored by Cerus Corporation.

Recruiting
Registry status
Phase 2
Development phase
70
Enrollment target
2
Study locations

NCT07015437 is a Phase 2 study of Healthy Subjects that is actively recruiting participants, run by Cerus Corporation. The registered enrollment target is 70 participants, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (45% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT07015437, a Phase 2 study of Healthy Subjects, is actively recruiting participants, sponsored by Cerus Corporation.

RECRUITING
Registry status
Phase 2
Development phase
70 participants
Enrollment target
2
Study locations

Study Summary

The objective of this trial is to assess the post-infusion viability of INTERCEPT RBCs by measuring the 24-hour post-infusion recovery and lifespan of autologous RBCs prepared with the INTERCEPT Blood System for RBC with AS-1 after 35 days post collection storage in comparison to untreated AS-1 RBCs stored for 35 days.

Conditions Studied

Interventions

  • DEVICE INTERCEPT Blood System for RBCs
  • OTHER Infusion of autologous radiolabeled RBCs

Study Locations (2)

Ohio

  • Hoxworth Blood Center - Cincinnati

Virginia

  • American Red Cross Research Laboratory - Norfolk

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2025-09-19
Est. Completion 2026-10-15
Phase Phase 2

Sponsor

Cerus Corporation

10 total trials

What the Registry Record Tells You About NCT07015437

The ClinicalTrials.gov registry entry for NCT07015437 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 128-participant average among 69 other Healthy Subjects trials with a reported enrollment target (45% lower). The listed sponsor is Cerus Corporation, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Subjects appearing as the primary indexed condition, and to 2 interventions - of which INTERCEPT Blood System for RBCs is the first listed.

NCT07015437 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Ohio, Virginia.

Frequently Asked Questions

What is clinical trial NCT07015437 about?

NCT07015437 is a clinical study titled "A Recovery and Lifespan Study Using INTERCEPT Red Blood Cells Prepared Using the INTERCEPT Blood System for RBCs With AS-1". The objective of this trial is to assess the post-infusion viability of INTERCEPT RBCs by measuring the 24-hour post-infusion recovery and lifespan of autologous RBCs prepared with the INTERCEPT Blood System for RBC with AS-1 after 35 days post collection storage in comparison to untreated AS-1 RBCs...

What is the current status of trial NCT07015437?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 70 participants. The study started on 2025-09-19. Estimated completion is 2026-10-15.

What conditions does trial NCT07015437 study?

This clinical trial studies the following conditions: Healthy Subjects.

What interventions are being tested in trial NCT07015437?

The interventions under investigation include: INTERCEPT Blood System for RBCs (DEVICE), Infusion of autologous radiolabeled RBCs (OTHER).

Who is sponsoring clinical trial NCT07015437?

This trial is sponsored by Cerus Corporation, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07015437 being conducted?

This trial has 2 study locations across Ohio, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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