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
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:
Secondary Objectives
Evaluations of immunogenicity as determined by:
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.
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.
Exclusion Criteria
History of any of the following medical illnesses
Any clinically significant abnormality detected on physical examination, including:
Any lab abnormality, as listed below:
50 µg Norwalk VLP Vaccine + Adjuvant/Excipients
Biological: Norwalk VLP Vaccine
100 µg Norwalk VLP Vaccine + Adjuvant/Excipients
Biological: Norwalk VLP Vaccine
14 mg chitosan, 3 mg mannitol, 3 mg sucrose, and 50 mcg MPL
Drug: Adjuvant/Excipients
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
intranasal,14 mg chitosan, 3 mg mannitol, 3 mg sucrose and 50 mcg of MPL, 2 doses 21 days apart
intranasal, puff of air, 2 doses, 21 days apart
intranasal, 50mcg, 2 doses--21 days apart
Intranasal, 100 mcg, 2 doses, 21 days apart
adverse events
Time frame: seven days
immunogenicity
Time frame: 28 days
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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