|
The trials will be conducted in two phases. The initial phase will involve 210 confirmed dengue patients to assess CP-COV03’s safety and efficacy. Patients will be divided into one placebo group (30 patients) and three experimental groups receiving varying doses (60 patients per group). Researchers will evaluate the drug’s ability to reduce viral load, improve symptoms, and analyze pharmacokinetic correlations to identify an optimal dosage for Phase 3 trials.
Dengue fever, prevalent primarily in tropical and subtropical regions, is transmitted by mosquitoes such as Aedes aegypti and Aedes albopictus. According to recent WHO statistics, dengue infections surpassed 14 million in 2024, with actual infections estimated around 400 million annually. No specific antiviral treatment exists currently, leaving symptomatic relief and fluid management as the primary interventions.
Oral antivirals offer a more feasible solution than vaccines for low- and middle-income countries due to lower costs and simplified logistics. If effective against multiple viral diseases with similar pathogenesis, a single drug like CP-COV03 could become a vital first-line response during outbreaks of emerging infectious diseases.
“These clinical trials go beyond simply treating dengue; they explore the potential of CP-COV03 as a universal antiviral effective against similar infections like Zika, chikungunya, and yellow fever,” said Bae Byung-joon, CEO of Hyundai Bioscience. “Leveraging the safety and efficacy proven in previous COVID-19 trials, we aim to introduce a new global paradigm for infectious disease treatment.”