drugset / Trial / NCT02343133

Safety Study of HemaMax™ (rHuIL-12) to Treat Acute Radiation Syndrome

NCT02343133

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether HemaMax is safe and well tolerated to support efficacy under FDA's Animal Rule to reduce the morbidity and mortality associated with the hematopoietic syndrome of acute radiation syndrome.

Timeline

Start
2015-01
Primary completion
2016-04
Completion
2016-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject INTERLEUKIN-12 HUMAN RECOMBINANT Unknown 12 ug Subcutaneous