This is a randomized, double-blind, placebo-controlled Phase 2/3 study to evaluate the efficacy, safety, and antiviral activity of CP-COV03 in adult patients with dengue infection.
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[Part 1] Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Timeframe: From start of study intervention (Day 1) up to end of safety follow-up (Day 29)
[Part 1] Average of dengue viral load on Day 3
Timeframe: Baseline, Day 1, 2, 3
[Part 2] Time to sustained symptom improvement up to Day 15
Timeframe: From baseline up to Day 15