drugset / Trial / NCT02653443
A Randomized, Multi-center, Open-label, Paired Controlled, Crossover In Vivo Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Autologous apheresis Conventional untreated Platelet Components | Unknown | — | Intravenous |
| Subject | Autologous apheresis Platelet Components | Unknown | — | Intravenous |
Indications
No indication recorded.