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Recruiting Phase 2, Phase 3 NCT07576868

NCT07576868 A Study of CP-COV03 Compared With Placebo in Participants With Dengue (Part 1) and Dengue-like Illness (Part 2)

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Clinical Trial Summary
NCT ID NCT07576868
Status Recruiting
Phase Phase 2, Phase 3
Sponsor Hyundai Bioscience Co., Ltd.
Condition Dengue
Study Type INTERVENTIONAL
Enrollment 210 participants
Start Date 2026-04-09
Primary Completion 2027-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
CP-COV03Placebo

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 210 participants in total. It began in 2026-04-09 with a primary completion date of 2027-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Patients who are 18 years or over of age at time of screening. * Patients who have at least two symptoms with a score of 2 or higher within 72 h from fever onset. * Patients who are diagnosed with dengue by NS1 positive (Phase 2- Part 1 only). And patients who are classified as dengue, zika, influenza, COVID-19 and others (Phase 3- Part 2 only) Exclusion Criteria: * Patients who show severe dengue (WHO dengue guideline C, any severe symptoms or clinical laboratory results) * Patients who have previously received dengue vaccine * Patients who have chronic medical conditions such as uncontrolled diabetes mellitus, severe asthma requiring oral steroids or admission to the hospital in the previous 6 months for cardiac disease

Contact & Investigator

Central Contact

Central Contact Person

✉ clinical@hyundaibio.com

📞 +82-1544-3194

Frequently Asked Questions

Who can join the NCT07576868 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Dengue. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07576868 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT07576868 currently recruiting?

Yes, NCT07576868 is actively recruiting participants. Contact the research team at clinical@hyundaibio.com for enrollment information.

Where is the NCT07576868 trial being conducted?

This trial is being conducted at Hanoi, Vietnam, Mỹ Tho, Vietnam.

Who is sponsoring the NCT07576868 clinical trial?

NCT07576868 is sponsored by Hyundai Bioscience Co., Ltd.. The trial plans to enroll 210 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology