Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02930226Phase 1Completed
Phase 1, randomised, double-blind trial of RePlas in hemorrhage and psychological trauma (6 arms), sponsored by U.S. Army Medical Research and Development Command. Primary endpoint: Safety of Single Infusions of FDP at Increasing Fixed Doses in Normal Healthy Subjects by Evaluating Vital Signs and Laboratory Tests at Day 29. Started Feb 2017; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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