grant

IND-enabling studies of an intranasal, single-replication M2SR influenza vaccine

Organization FLUGEN, INC.Location MADISON, UNITED STATESPosted 1 Aug 2015Deadline 30 Jun 2026
NIHUS FederalResearch GrantFY202521+ years old65 and older65 or older65 years of age and older65 years of age or more65 years of age or older65+ years65+ years oldAccelerationAddressAdultAdult HumanAdvanced DevelopmentAged 65 and OverAirway infectionsAnimal ModelAnimal Models and Related StudiesAnimalsAntibodiesAntibody titer measurementAssayAustraliaAvesAvianBioassayBiological AssayBirdsBlood SerumCategory C pathogenCategory C priority pathogenCell BodyCell LineCellLineCellsCessation of lifeClinical EvaluationClinical ResearchClinical StudyClinical TestingClinical TrialsDNADNA mutationDeathDeoxyribonucleic AcidDevelopmentDistantElderlyEvaluationFerretsGeneralized GrowthGenetic ChangeGenetic defectGenetic mutationGrippeGrowthH1N1H1N1 VirusH3N2H3N2 VirusH5N1H5N1 virusHealthHemagglutininHospital AdmissionHospitalizationHumanIND FilingIND applicationIND packageIND submissionImmune responseImmunityInactivated VaccinesInactivated Virus VaccineIndividualInfluenzaInfluenza AInfluenza A H5N1Influenza A Virus, H1N1 SubtypeInfluenza A Virus, H3N2 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza A virusInfluenza BInfluenza B VirusInfluenza VaccinesInfluenza VirusInfluenza Viruses Type AInfluenza Viruses Type BInfluenzavirus AInvestigational New Drug ApplicationKilled VaccinesModern ManMorbidityMorbidity - disease rateMucosaMucosal TissueMucous MembraneMutationNIAIDNational Institute of Allergy and Infectious DiseaseNational SecurityOrthomyxovirus Type AOrthomyxoviruses Type BPathogenicityPopulationProcessProductionProteinsPublic HealthQualifyingReagentRecommendationRecordsReportingResidualResidual stateRespiratory DiseaseRespiratory InfectionsRespiratory System DiseaseRespiratory System DisorderRespiratory Tract InfectionsRunningSafetySeasonsSerumSpecific qualifier valueSpecifiedStrains Cell LinesT cell responseTestingTissue GrowthTrainingType A InfluenzaUpdateVaccinationVaccine AntigenVaccine ProductionVaccinesVialVial deviceVirusabove age 65access to vaccinationaccess to vaccinesadulthoodadvanced ageafter age 65age 65 and greaterage 65 and olderage 65 or olderageage of 65 years onwardagedaged 65 and greateraged 65+aged ≥65analytical methodantibody titeringavian influenza H5N1avian influenza H5N1 viruscell bankclinical testcross immunitycross protectioncross reactivitycultured cell linedevelopmentaleggexperimentexperimental researchexperimental studyexperimentsflasksfluflu serotypeflu strainflu subtypeflu vaccineflu viral strainflu virus pandemicflu virus strainflu virus vaccinegenome mutationgeriatrichost responsehuman old age (65+)immune response to vaccinationimmune response to vaccinesimmune system responseimmunogenicityimmunoresponseinfluenza serotypeinfluenza straininfluenza subtypeinfluenza viral straininfluenza virus pandemicinfluenza virus straininfluenza virus vaccineinfluenzavirusmanufacturemanufacturing processmodel of animalmortalitymultidisciplinaryneutralizing antibodynovelontogenyover 65 yearspan influenza vaccinepan influenza viral vaccinepan influenza virus vaccinepandemic flupandemic influenzapandemic strain of influenzapandemic virusproduce vaccinesprototyperesearch clinical testingseasonal fluseasonal influenzasenior citizenseropositiveuniversal flu vaccineuniversal influenza vaccineuniversal influenza virus vaccineuniversal vaccine against fluuniversal vaccine against influenzavaccination accessvaccination availabilityvaccine accessvaccine against fluvaccine against influenzavaccine associated immune responsevaccine availabilityvaccine effectivenessvaccine efficacyvaccine immune responsevaccine immunogenicityvaccine induced immune responsevirtual≥65 years
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Full Description

ABSTRACT
Influenza (flu) virus, an NIAID category C priority pathogen, causes a respiratory disease resulting in over 200,000 hospitalizations and ~ 36,000 deaths per year in the US, while global influenza pandemics have resulted in as many as 50-100 million deaths worldwide. To address this threat to public health, annual vaccination is recommended for all individuals aged over 6 months in the US. However, currently available vaccines are lacking in efficacy. CDC’s vaccine effectiveness (VE) estimates for the 2014-2015 influenza season was only 23%. The reduced protection was attributed to the fact that the circulating viruses had drifted from the H3N2 vaccine virus recommended for vaccine production. In fact overall VE from 2005-2016 ranges from 10% to 60% at best. Current influenza vaccines, live or inactivated, offer suboptimal protection when matched and do not provide protection when the vaccine is mismatched.

FluGen has developed a novel M2-deficient influenza vaccine (M2SR) that provides effective heterosubtypic protection in animal models. In addition, we have shown that an H1N1 M2SR elicits protection against drifted H1N1 viruses in ferrets. Moreover, H1N1 M2SR provided protection against lethal H5N1 pandemic virus in ferrets. A prototype H3N2 M2SR vaccine, shown to be generally safe and well-tolerated in clinical trials and elicited immune responses in healthy adult subjects who were seronaive, seropositive and seroprotected.

The H3N2 M2SR also provided protection against a highly drifted influenza virus in a human challenge trial.

In this project, we propose to further develop M2SR as a quadrivalent (Quad) universal influenza vaccine that provides effective protection against drifted influenza viruses in the following specific aims: Aim 1a. Transfer of M2SR and BM2SR production platforms to US-based CMO. Aim 1b. Analytical method transfer, development and qualification at US-based CMO.

These activities will accelerate development of the M2SR influenza vaccine toward a quadrivalent vaccine product that can provide broad cross-protection against drifted influenza viruses.

Grant Number: 5SB1AI120269-06
NIH Institute/Center: NIH

Principal Investigator: Pamuk Bilsel

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