The primary objective of this study is to evaluate the pharmacokinetic profile of a single dose of IVIb administered over 5-7 minutes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
12
800mg IVIb diluted in 200mL NS will be given IV (in the vein) concurrently with an oral placebo on Day 1 and 200ml Normal Saline will be given IV (in the vein)concurrently with 800mg oral ibuprofen on Day 8
Centre for Pharmaceutical Research
Underdale, South Australia, Australia
To evaluate the pharmacokinetic profile of a single dose of IVIb administered over 5-7 minutes.
Time frame: 12 hours
To evaluate the safety and tolerability of a single dose of IVIb in healthy adult participants.
Time frame: 12 hours
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