drugset / Trial / NCT02310412

A Controlled, In Vivo, Pilot Study to Assess the Recovery and Survival of Radiolabeled Autologous INTERCEPT Treated 7-Day Stored Apheresis Platelet Components in 35% Plasma and 65% InterSol and 7-Day Stored Apheresis Platelet Components in 100% Plasma

NCT02310412 ↗

Phase 2 Completed 14 enrolled Cerus Corporation
RandomizedParallel-groupOpen-labelOther

Summary

The objective of this study is to test the hypothesis that INTERCEPT platelet components stored for 7 days retain sufficient viability for therapeutic efficacy. The post-infusion recovery and lifespan of 7-day old INTERCEPT platelet components stored in 35% plasma and 65% InterSol or stored in 100% plasma, will be measured in comparison to "fresh" radiolabeled platelets according to FDA guidance for platelet testing (FDA 1999).

Timeline

Start
2014-12
Primary completion
2015-05
Completion
2015-09

Drugs

EvaluationDrugModalityDoseRoute
Subject INTERCEPT treated platelets Unknown — —

Indications

No indication recorded.