2246855
Last Update Posted: 2018-02-27
Recruiting has ended
All Genders accepted | Under |
Estimated Participants | No Expanded Access |
Interventional Study | Accepts healthy volunteers |
A Comparison of the Pharmacokinetics, Safety and Tolerance of Two Formulations of a Liquid IVIg in Healthy Volunteers
The main object of the study is to compare the AUC0-84, of a single intravenous infusion of Vigam® Liquid (infused at the licensed rate of up to 3mL/min) with Gammaplex® (infused at up to 3mL/min and up to 6mL/min).
Eligibility
Relevant conditions:
Healthy
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Inclusion criteria
Exclusion criteria
locations
Contact Information
Overall Contact
No valid contacts available
Data sourced from ClinicalTrials.gov