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CompletedNCT00806962Updated May 6, 2015

Phase 1 Norwalk Vaccine Study

A Phase 1 interventional study of Adjuvant/Excipients and placebo in Norovirus, sponsored by LigoCyte Pharmaceuticals, Inc.. Completed at 4 sites in United States. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-05-06.

Sponsored by LigoCyte Pharmaceuticals, Inc. · Phase 1, Interventional, and Prevention

Phase
Phase 1
Study type
Interventional
Enrollment
61
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

Randomized, double blind, multi-site, study in healthy adults, comparing safety and immunogenicity of two dosage levels of Norwalk VLP Vaccine with adjuvant/excipients and with placebo controls

Primary Objective:

  • Safety as determined by occurrence of local intranasal symptoms or other symptoms as reported by a self-administered memory aid for 7 days after each vaccination and hematology, blood chemistry and physical examinations performed by the clinical research staff
  • Subjects will also be monitored for Serious Adverse Events (SAEs), and onset of any new medical conditions for 180 days following the last study vaccinations (Day 201).

Secondary Objectives

Evaluations of immunogenicity as determined by:

  • Geometric mean titers and seroconversion rate of serum anti- Norwalk VLP IgG and IgA
  • Stimulation of anti-Norwalk VLP IgA antibody secreting cells (ASC)
  • Presence of antigen specific memory B-cell response

Cells will be collected and stored for possible future evaluation of Norwalk VLP-specific cell-mediated immune (CMI) responses

Study Hypothesis:

The incidence of adverse events after intranasal Norwalk VLP Vaccine will be the same as the incidence of adverse events after intranasal adjuvant/excipients alone. Norwalk VLP Vaccine and adjuvant/excipients will have a higher incidence of mild to moderate nasal adverse events compared to placebo but similar incidence of other adverse events.

Two doses of the 100 µg of Norwalk VLP Vaccine will be more immunogenic than two doses of 50 µg of Norwalk VLP Vaccine. The post-vaccination serum antibody responses, the number of antibody secreting cells (ASC) and IgG and IgA memory B-cell responses directed against Norwalk Virus antigen will be increased after Norwalk VLP Vaccine compared to adjuvant/excipients and to placebo.

02

Conditions studied

  • Norovirus
03

In context

Lead sponsor

This is the only study on the registry with LigoCyte Pharmaceuticals, Inc. as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Signed written informed consent
  2. Age 18 - 50 years, inclusive
  3. Good general health as determined by a screening evaluation within 30 days before administration of Norwalk VLP Vaccine, adjuvant/excipients or placebo
  4. Expressed interest and availability to fulfill the study requirements
  5. Agrees not to become pregnant from the time of study enrollment until at least 56 days after the last administration of Norwalk VLP Vaccine, adjuvant/excipients or placebo; if a woman is sexually active and capable of conception (i.e., no history of hysterectomy or tubal ligation), she must agree to use hormonal or barrier birth control. A woman is eligible if she is monogamous with a male who has had a vasectomy.
  6. Demonstrated to be an H type-1 antigen secretor
  7. Agrees not to participate in another clinical trial with an investigational product for the entire duration of the study (six months after the last study dose i.e. 201 days)
  8. Agrees to storage of unused clinical specimens for an indefinite period of time only for those specimens collected by the University of Maryland CVD for use in future research at the CVD. [A University of Maryland site-specific inclusion criterion]

Exclusion criteria

Exclusion Criteria

  1. History of any of the following medical illnesses

    • Chronic rhinitis, runny nose, sneezing
    • Clinically significant nose bleed within the last year
    • Diabetes
    • Cancer
    • Heart disease (hospitalization for a heart attack, arrhythmia, or syncope)
    • Unconsciousness (other than a single brief "concussion")
    • Seizures (other than febrile seizures as a child \<5 years old)
    • Recurrent infections (more than 3 hospitalizations for invasive bacterial infections such as pneumonia or meningitis)
    • Asthma requiring treatment with inhaler or medication
    • Any current illness requiring daily medication other than vitamins, birth control, or anti-depressant
  2. Blood Type B or AB, regardless of Rh + or -
  3. Allergies or hypersensitivity to chitosan, shrimp, other shellfish or any component of the vaccine, adjuvant/excipients or placebo
  4. History of nasal surgery of any type (including tonsilectomy/adenoidectomy)
  5. Any clinically significant abnormality detected on physical examination, including:

    • Murmur (other than a functional murmur)
    • Focal neurological abnormality
    • Hepatosplenomegaly
    • Lymphadenopathy
    • Jaundice
  6. Hypertension (BP > 140/90 mm Hg on two separate days)
  7. Any lab abnormality, as listed below:

    • Neutrophils (WBC) outside the normal range
    • Hemoglobin outside the normal range (may be repeated once if outside this limit)
    • Platelet count outside the normal range (may be repeated once if outside this limit)
    • Creatinine outside the normal range (may be repeated once if outside this limit)
    • Glucose > upper limit of normal (may be repeated once if outside this limit)
    • AST or ALT outside the normal range (may be repeated once if outside this limit)
    • Positive serology for hepatitis C or HIV antibody or hepatitis B surface antigen
  8. For women, positive serum pregnancy test within 7 days and urine pregnancy test within 24 hours of administering either dose of Norwalk VLP Vaccine, adjuvant/excipients or placebo
  9. Nursing mother
  10. Temperature > 38.0 degrees C (100.4 degrees F) or symptoms of an acute self-limited illness such as an upper respiratory infection or gastroenteritis within 3 days of administration of Norwalk VLP Vaccine, adjuvant/excipients or placebo
  11. Previous participation in a study of Norovirus vaccines
  12. Medical, occupational, or family problems as a result of alcohol or illicit drug use during the past 12 months
  13. Receipt of an investigational vaccine or drug within 28 days before administration of Norwalk VLP Vaccine, adjuvant/excipients or placebo
  14. Other condition that in the clinical judgment of the investigator would jeopardize the safety or rights of a subject participating in the trial, would render the subject unable to comply with the protocol or would interfere with the evaluation of the vaccine
  15. Failure to pass written examination about this study (70% correct answers required to pass)[A University of Maryland site-specific exclusion criterion]
05

Study design

Phase
Phase 1
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
61 participants (actual)

Study arms

  • Experimental
    Vaccine Arm 1

    50 µg Norwalk VLP Vaccine + Adjuvant/Excipients

    Biological: Norwalk VLP Vaccine

  • Experimental
    Vaccine Arm 2

    100 µg Norwalk VLP Vaccine + Adjuvant/Excipients

    Biological: Norwalk VLP Vaccine

  • Active comparator
    Adjuvant/Excipients (MPL)

    14 mg chitosan, 3 mg mannitol, 3 mg sucrose, and 50 mcg MPL

    Drug: Adjuvant/Excipients

  • Sham comparator
    Empty device

    Empty device that contains no dry powder formulation. Actuation of the empty intranasal delivery device will deliver a puff of air per device.

    Device: placebo

Interventions

  • DrugAdjuvant/Excipients

    intranasal,14 mg chitosan, 3 mg mannitol, 3 mg sucrose and 50 mcg of MPL, 2 doses 21 days apart

  • Deviceplacebo

    intranasal, puff of air, 2 doses, 21 days apart

  • BiologicalNorwalk VLP Vaccine

    intranasal, 50mcg, 2 doses--21 days apart

  • BiologicalNorwalk VLP Vaccine

    Intranasal, 100 mcg, 2 doses, 21 days apart

06

What researchers measure

Primary outcomes

  1. adverse events

    Time frame: seven days

Secondary outcomes

  1. immunogenicity

    Time frame: 28 days

07

Study locations

4 sites
  • University of Maryland Center for Vaccine Development
    Baltimore, Maryland, United States
  • Saint Louis University
    Saint Louis, Missouri 63104, United States
  • University of Rochester Medical Center
    Rochester, New York 14642, United States
  • Cincinnati Children's Hospital
    Cincinnati, Ohio 45229, United States
08

References and documents

Publications

  • El-Kamary SS, Pasetti MF, Mendelman PM, Frey SE, Bernstein DI, Treanor JJ, Ferreira J, Chen WH, Sublett R, Richardson C, Bargatze RF, Sztein MB, Tacket CO. Adjuvanted intranasal Norwalk virus-like particle vaccine elicits antibodies and antibody-secreting cells that express homing receptors for mucosal and peripheral lymphoid tissues. J Infect Dis. 2010 Dec 1;202(11):1649-58. doi: 10.1086/657087. Epub 2010 Oct 27. Erratum In: J Infect Dis. 2011 Apr 1;203(7):1036. PubMed 20979455 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 6, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00806962
Lead sponsor
LigoCyte Pharmaceuticals, Inc.
Responsible party
Sponsor
First posted
Dec 11, 2008
Start date
Nov 2008
Primary completion
Oct 2009
Completion
Oct 2009
Last update
May 6, 2015

Study contacts

John J Treanor, MD
principal investigator · University of Rochester

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2015. You cannot join it, but the record below documents what was studied.

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