ClinicalTrials.gg
Not yet recruitingNCT07831473Updated Sep 21, 2026

Phase I Study of VLPDEN-02 Dengue Vaccine in Healthy Adults

A Phase 1 interventional study of VLPDEN-02 1.0 µg (0.25 µg of each VLP) + ALFQ adjuvant and VLPDEN-02 10 µg (2.5 µg of each VLP) + ALFQ adjuvant in Randomised Clinical Trial, Double Blind and Dengue, sponsored by VLP Therapeutics. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-21.

Sponsored by VLP Therapeutics · Phase 1, Interventional, and Prevention

Phase
Phase 1
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

This is a Phase 1, randomized, double-blind, placebo-controlled, dose escalation study. Forty-two flavivirus-naïve adults will be enrolled and will receive 3 administrations of VLPDEN-02 or control at days 0, 28, and 56. Three dose-cohorts of VLPDEN-02 will be evaluated (1 µg, 10 µg, and 100 µg) in a dose-escalation strategy. Each dose cohort will enroll 14 participants (10 VLPDEN-02 recipients and 4 control recipients).

Read the detailed description

VLPDEN-02 is a non-infectious vaccine candidate comprised of four VLPs, each corresponding to a different dengue serotype (DENV-1-4), mixed in equal quantities.

02

Conditions studied

  • Randomised Clinical Trial
  • Double Blind
  • Dengue
  • Challenge Test
  • Dose Escalation and Safety

Browse trials for

Keywords

  • Dengue
  • VLP
  • Dengue fever
  • DENV
  • challenge model
  • reactogenicity
  • ALFQ
03

In context

Dengue

283 studies on the registry are indexed under Dengue; 44 are open to participants now.

This study's planned enrollment of 42 is below the median of 132 across 197 interventional studies indexed under Dengue.

Browse Dengue studies →

Lead sponsor

VLP Therapeutics is the lead sponsor of 3 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Male or female between 18 and 55 years of age, inclusive, at the time of screening.
  2. Able and willing to comply with all research requirements, in the opinion of the investigator.
  3. Good general health as determined by physical examination, laboratory screening, and review of medical history.
  4. Available for the duration of the study, which is approximately 50 weeks.
  5. Willingness to participate in the study as evidenced by signing the document.
  6. Participant has 12-lead (ECG*) and clinical laboratory evaluations at screening with no abnormalities, as assessed by the investigator. *A normal ECG is defined as the presence of normal sinus rhythm (heart rate 45-100 beats per minute [bpm], inclusive) and the absence of:

    1. corrected by Fridericia (QTcF) >450 milliseconds (ms) in male participants or >460 ms in female participants;
    2. PR interval >220 ms;
    3. QRS duration ≧ 110ms;
    4. Complete left or right bundle branch block;
    5. 2nd or 3rd degree atrioventricular block;
    6. Sustained ventricular or atrial arrhythmia;
    7. ST elevation consistent with cardiac ischemia;
    8. Ventricular or atrial premature contractions in couplets or higher order groupings.
  7. Females only: Female participants must meet one of the following two (2) criteria:

    1. No due to status (12 months of natural) [spontaneous] amenorrhea or surgical procedure such as hysterectomy, bilateral oophorectomy, bilateral salpingectomy, tubal coil/Essure or tubal ligation, females in a monogamous relationship with a vasectomized male partner or females who exclusively have sex with female partners.
    2. Female participants of agree to practice highly effective before enrollment and through 60 days post-DENV-3 challenge using one of the following methods: condoms (male or female) with spermicide; diaphragm, or cervical cap with spermicide; intrauterine device; contraceptive pills, patch, injection, intravaginal ring or other FDA-approved contraceptive method; male partner has previously undergone a vasectomy; abstinence (> 6 months since last sexual encounter). Vasectomized partner is a highly effective contraceptive method provided that the partner is the sole sexual partner of the person of childbearing potential and the absence of sperm has been confirmed. If not, additional highly effective method(s) of contraception should be used.
  8. Male participants are encouraged but not required to practice highly effective contraception to avoid pregnancy in their partner from 30 days prior to enrollment through 60 days post-DENV-3 challenge.
  9. Females of childbearing potential must agree to not donate ova or oocytes during the study. Males must refrain from sperm donation during the study
  10. Have an available phone running iOS 15.0 or later or Android phone running software v7.0 or higher, willing to download the myMedidata app, and willing to complete daily electronic diaries when required.

Exclusion criteria

Exclusion Criteria:

  1. Females only: Currently pregnant, as determined by positive beta-human choriogonadotropin (beta-HCG) test, or breast-feeding.
  2. The participant has a history of significant alcoholism or drug/chemical abuse within 12 months prior to enrollment that has caused medical, occupational, or family problems as indicated by participant history.
  3. Any medical, psychiatric, social condition, occupational reason or other responsibility that, in the judgment of the investigator, is a to protocol participation or impairs a participant's ability to give .
  4. A participant with a confirmed screening laboratory value of Grade 1 or above for (ANC), (ALT), or serum creatinine. Values of Grade 1 or above for these tests may be repeated to confirm a Grade 1 or above value. Abnormal laboratory values other than those specified will not be exclusionary if the clinician deems them not .
  5. Any other significant disease, disorder or finding which may significantly increase the risk to the participant because of participation in the study, affect the ability of the participant to participate in the study or impair interpretation of the study data, in the judgment of the Investigator.
  6. Asplenia (absence of normal spleen function).
  7. History of confirmed or suspected immunodeficiency.
  8. Asthma that is unstable requiring emergent care, urgent care, hospitalization or intubation during the past 6 months.
  9. Diabetes mellitus (type I or II) currently requiring medication for control.
  10. Hypertension that is not well controlled by medication prior to enrollment. Two repeat measurements are allowed more than 10 minutes apart in the absence of any other concerning health screening issues.
  11. Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or disorder requiring special precautions) or significant bruising or bleeding difficulties with intramuscular injections or blood draws.
  12. History of chronic or active neurologic diseases including seizure disorder and chronic migraine headaches. Exceptions are: i) childhood febrile seizures, or ii) seizures secondary to alcohol withdrawal more than three [3] years ago.
  13. Participants receiving any of the following substances:

    1. Systemic medications or cytotoxic medications within 12 weeks before enrollment [with the exception of a short course of (≤14 days duration or a single injection) for a self-limited condition at least two (2) weeks before enrollment; inhaled, intranasal or topical steroids are not considered exclusionary].
    2. Receipt of any within 28 days before or after VLP vaccination.
    3. Receipt of medically indicated non-live vaccine, (e.g. influenza, pneumococcal), or allergy treatment with antigen injections, planned for administration seven (7) days before or after study vaccine administration.
  14. Participant has a positive urine drug toxicology at screening for drugs of abuse defined as Amphetamines, Barbiturates, Benzodiazepines, Cocaine Metabolite, Opiates, Oxycodone, Phencyclidine without confirmation of medical need (e.g. anxiolytics or pain medications).
  15. Women with a positive pregnancy test at screening, vaccination day or challenge day.
  16. infection, by screening and confirmatory assays.
  17. Participant is seropositive for surface antigen (HBsAg) or positive for RNA at screening.
  18. Participant has definite plans to travel to a dengue-endemic area during the study.
  19. Participant has history or documentation of previous infection with DENV, ZIKV, WNV, JEV, YFV, or St. Louis encephalitis virus (SLEV). Previous infection with DENV, ZIKV, WNV or YFV will be determined by neutralizing antibody assay performed within 60 days of enrollment, medical record, or vaccination record. JEV or SLEV infection will be assessed based on participant history and available medical records. JEV vaccination history will also be reviewed.
  20. History of a severe allergic reaction or anaphylaxis.
  21. History of allergy to hygromycin.
  22. Receipt of blood products within the past 6 months, including transfusions or immunoglobulin or anticipated receipt of any blood products or immunoglobulin during the 28 days following vaccination.
  23. Anticipated receipt of any agent in the 28 days before or through the duration of the trial.
  24. Refusal to allow storage of specimens for future research.
  25. Participant is a JHU student currently enrolled in a coursework, an internship, or clinical hours where the supervisor or instructor of record is employed by the Center for Immunization Research.
  26. Participant is faculty or staff currently employed by the Center for Immunization Research.
Terms in these criteria, in plain language(19)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

QT and QTc

On an ECG, the QT interval is the time the heart’s lower chambers take to activate electrically and recover in each beat. QTc is that time adjusted for heart rate (QTcF by Fridericia’s formula, QTcB by Bazett’s). Some medicines lengthen it, and a long QTc can raise the risk of a dangerous heart rhythm.

The study may name a correction formula and a limit in milliseconds, often around 450–480.

Reproductive potential

Able to have children. For women this usually means from the first period until menopause, unless permanently unable to through surgery; for men, unless permanently sterile. Read who the line is about — participants, women, men, or their partners.

Criteria about it usually ask for contraception during the study and for a time after it.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Absolute neutrophil count (ANC)

The number of neutrophils, white blood cells that help fight infection, in a given amount of blood. Too few raises the risk of infection.

It is a count, not a percentage of the white cells. Limits are written in units that mean the same: ≥ 1.5 × 10⁹/L is ≥ 1,500 per mm³ (µL). Each lab has its own reference range.

ALT and AST (liver enzymes)

Two enzymes measured in a routine blood test of the liver. Higher levels can mean the liver is under strain or damaged. SGPT and SGOT are older names for ALT and AST.

Criteria usually give a limit as a multiple of the upper limit of normal (ULN), often higher when cancer has spread to the liver.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

05

Study design

Phase
Phase 1
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Sequential assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
42 participants (estimated)

Study arms

  • Experimental
    Cohort A

    VLPDEN-02 1.0 µg + ALFQ adjuvant vs. Control ALFQ adjuvant alone - 3 doses 28 days apart

    Biological: VLPDEN-02 1.0 µg (0.25 µg of each VLP) + ALFQ adjuvant · Biological: ALFQ adjuvant + Saline · Biological: rDEN3Delta30

  • Experimental
    Cohort B

    VLPDEN-02 10 µg + ALFQ adjuvant vs. Control ALFQ adjuvant alone - 3 doses 28 days apart

    Biological: VLPDEN-02 10 µg (2.5 µg of each VLP) + ALFQ adjuvant · Biological: ALFQ adjuvant + Saline · Biological: rDEN3Delta30

  • Experimental
    Cohort C

    VLPDEN-02 100.0 µg + ALFQ adjuvant vs. Control ALFQ adjuvant alone - 3 doses 28 days apart

    Biological: VLPDEN-02 100 µg (25 µg of each VLP) + ALFQ adjuvant · Biological: ALFQ adjuvant + Saline · Biological: rDEN3Delta30

Interventions

  • BiologicalVLPDEN-02 1.0 µg (0.25 µg of each VLP) + ALFQ adjuvant

    VLPDEN-02 is comprised of 4 virus-like particles (VLPs) each containing the Pre-membrane (prM), and envelope (E) of either DENV-1, DENV-2, DENV-3 or DENV-4. Mixed 1:1 with Army Liposome Formulation containing QS21 saponin (ALFQ).

  • BiologicalVLPDEN-02 10 µg (2.5 µg of each VLP) + ALFQ adjuvant

    VLPDEN-02 is comprised of 4 virus-like particles (VLPs) each containing the Pre-membrane (prM), and envelope (E) of either DENV-1, DENV-2, DENV-3 or DENV-4. Mixed 1:1 with Army Liposome Formulation containing QS21 saponin (ALFQ).

  • BiologicalVLPDEN-02 100 µg (25 µg of each VLP) + ALFQ adjuvant

    VLPDEN-02 is comprised of 4 virus-like particles (VLPs) each containing the Pre-membrane (prM), and envelope (E) of either DENV-1, DENV-2, DENV-3 or DENV-4. Mixed 1:1 with Army Liposome Formulation containing QS21 saponin (ALFQ).

  • BiologicalALFQ adjuvant + Saline

    Army Liposome Formulation containing QS21 saponin (ALFQ) adjuvant mixed 1:1 with saline

  • BiologicalrDEN3Delta30

    rDEN3Delta30 is an under-attenuated DENV-3 derived from the naturally attenuated DENV-3 Sleman/78 strain. It will be administered subcutaneously (SC) at a dose of 1,000 plaque-forming units (PFU).

06

What researchers measure

Primary outcomes

  1. Safety and Reactogenicity Assessment

    The primary objective of this Phase 1 clinical trial is to assess the safety and reactogenicity of three doses of VLPDEN-02 for 7 days post vaccination compared with placebo control as determined by solicited local and systemic reactogenicity.

    Time frame: Injection to 7 days post vaccination

Secondary outcomes

  1. Immunogenicity Assessment

    To assess the immunogenicity of VLPDEN-02 vaccine after each vaccination.

    Time frame: Initial injection to day 168

  2. Protective Efficacy to Dengue 3 Challenge

    To assess the protective efficacy of VLPDEN-02 vaccine against viremia induced by 10\^3 PFU of the DENV-3 challenge strain rDEN3Delta30 administered approximately 4 months post-third vaccination.

    Time frame: Day 168 to Day 348

  3. Protective efficacy against rash induction

    To assess the protective efficacy of VLPDEN-02 against rash induced by 10\^3 PFU of the DENV-3 challenge strain rDEN3Delta30 administered approximately 4 months post-third vaccination.

    Time frame: Day 168 to Day 348

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — VLPDEN-02 is proprietary vaccine in early development

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07831473
Lead sponsor
VLP Therapeutics
Collaborators
Global Health Innovative Technology Fund
Responsible party
Sponsor
First posted
Sep 21, 2026
Start date
Jan 4, 2027 (estimated)
Primary completion
Mar 15, 2028 (estimated)
Completion
May 15, 2028 (estimated)
Last update
Sep 21, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion