drugset / Trial / NCT02653443

A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study

NCT02653443 ↗

Phase 2 Terminated 14 enrolled Cerus Corporation
RandomizedCrossoverOpen-labelOther

Summary

The objective of this study is to test the hypothesis that INTERCEPT Blood System for platelet components stored for 6 or 7 days after INTERCEPT Blood System treatment retain sufficient viability for therapeutic efficacy. The post-infusion recovery and lifespan of autologous INTERCEPT Blood System for platelet components in 35% plasma/65% InterSol (Test platelets) stored for 6 or 7 days will be measured in comparison to "fresh" autologous radiolabeled platelets (Control platelets) according to FDA guidance for platelet testing (FDA 1999). Recovery and lifespan results between components stored for 6 and 7 days will also be assessed.

Timeline

Start
2015-12
Primary completion
2016-05
Completion
2016-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Autologous apheresis Conventional untreated Platelet Components Unknown — Intravenous
Subject Autologous apheresis Platelet Components Unknown — Intravenous

Indications

No indication recorded.