This is a single center, sequential-cohort, double-blind, placebo-controlled, multiple ascending dose (MAD), 7-day treatment period study in healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
36
BTA-C585; Multiple ascending doses from 100 mg to 600 mg
Multiple ascending doses to match 100 mg to 600 mg BTA-C585 capsules
Biota Investigational Site
San Antonio, Texas, United States
Area under the plasma concentration-time curve (AUC) from time 0 to 24 hours
Time frame: 0-24 hours
Number of adverse events
Time frame: Day -1 to Day 14
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