GLASSIA Infusion Rate Study

Authors
Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2012
The purpose of this study was to generate sufficient safety and tolerability information in support of an increase in the infusion rate of intravenous GLASSIA in the prescribing information from 0.04 to 0.2 mL/kg/min.
Epistemonikos ID: e9c4fd923b354505c4a3b57fad82eb9141562be5
First added on: May 11, 2024