This is a phase Ib, randomized, double-blind, placebo-controlled study to evaluate safety, tolerability, efficacy and pharmacokinetics of ASC10 tablets in mild or moderate COVID-19 subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Pinnacle Research Group
Anniston, Alabama, United States
Aga Clinical Trials
Hialeah, Florida, United States
Number of participants with Treatment Emergent Adverse Event (TEAEs) in multiple ascending doses
Time frame: From Day 0 to Study Completion, up to 32 days
PK parameters for ASC10, GLC01-700 (molnupiravir) and ASC10-A in plasma as AUC0-12h
Time frame: From Day 1 to Day 6
Time (days) to sustained resolution of all targeted COVID-19 signs/symptoms
Time frame: From Day 1 to Study Completion, up to 32 days
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