About this trial
This study aims to conduct a safe human infection challenge using an attenuated serotype DEN3 dengue virus in adult volunteers. The clinical, viral and immune response characteristics of the model will be analysed to understand the pathophysiology of dengue fever. This data will be used to inform future studies, including a planned follow up study (DEN-CHIM-02) which will investigate the efficacy of an investigational dengue vaccine at protecting against DEN3 infection.
Study conditions that result in a safe, reproducible infection in ≥80% of research participants (attack rate) with the DEN3 challenge agent have been identified during studies conducted by our collaborators in the US. This includes the inoculum dose, safety monitoring, and necessary participant pre-screening to exclude prior Orthoflavivrus infection or vaccinations.
Study objectives are to:
1. Establish in seronegative volunteers in Singapore a safe DENV controlled human infection (CHI) model, with an infection rate of ≥80%, suitable for future studies of interventions. 2. Characterise the clinical, haematological and virological response following controlled inoculation of the attenuated DEN3 challenge agent. 3. Conduct deep immunophenotyping to understand the cellular, humoral and innate immune response to dengue infection. 4. Explore the longitudinal immune response in the 3 years after challenge, including following subsequent dengue vaccination.
Eligibility criteria
Qualifiers
An informed consent form (ICF) has been signed and dated by the participant, an investigator, and a witness
Adult, aged between 21 and 45 years, inclusive (at the time of consent)
No known history of prior dengue, zika or other Orthoflavivirus infection
No history of prior dengue, yellow fever, Japanese encephalitis virus, or other Orthoflavivirus vaccination
Disqualifiers
History or evidence of any clinically significant or currently active neurologic, cardiac, pulmonary, hepatic, rheumatologic, autoimmune, or renal disease.
History of active depression and/or anxiety with associated severe psychiatric comorbidities, for example psychosis.
Behavioural, cognitive, or psychiatric disease that in the opinion of the investigator affects the ability of the subject to understand and cooperate with the requirements of the study protocol.
Significant history or presence of drug or alcohol misuse
Trial design
Treatments tested in this trial
- GMP-produced rDEN3delta30 virus
Treatment groups
Sponsors and collaborators
Tan Tock Seng Hospital
Lead sponsor
A*Star
Collaborator
Duke-NUS Graduate Medical School
Collaborator
Nanyang Technological University
Collaborator