Grant: Operating Grant: Clinical Trials Projects - Indirect Costs
McMaster University
$2,066,579.00
A phase 2 trial to evaluate safety and immunogenicity of a next-generation COVID-19 vaccine delivered by inhaled aerosol to humans
EF 2022-23
Résumé
Despite the benefit of current COVID vaccines in preventing severe disease and death, these vaccines are relatively poor at preventing infection with new variants like Omicron and work less well in the elderly and people with weak immune systems. There is an urgent need to develop new, next generation vaccines. As leaders in respiratory mucosal immunity, we have shown how delivering a vaccine directly to the lung by inhalation leads to better protection from infection than an IM injection. Before COVID, we were studying a new viral-vectored vaccine for TB inhaled into the lungs in healthy volunteers. We showed that this vaccine was safe and that good immune responses to TB were made in the lungs.
With the arrival of COVID, we developed next generation multivalent COVID-19 vaccines active against not only the spike protein but also internal viral proteins that do not mutate, even in variants. After showing that these vaccines were safe and protected against COVID infection in animals, we began a human trial with 30 healthy persons who had at least 2 doses of a mRNA vaccine and are studying in detail the immune responses in the lung and blood.
In our planned placebo-controlled Phase 2 study, we will enroll 500 participants from at least 3 clinical trial sites across Canada, to get more confidence in the safety of the inhaled route of administration and make the results more generalizable by enrolling older persons and those with underlying health conditions. We will gather safety and measures of immune responses to support a phase 3 clinical trial, with the goal of licensing and marketing our made-in-Canada vaccine and the aerosol method of administration. We expect this vaccine approach to be effective in breaking the cycle of new variant, poor vaccine performance, transmission and infection. The research team is led by Dr Fiona Smaill and includes members with a rich experience in vaccine clinical trials, vaccine manufacturing, aerosol delivery, and immunology.
Programme
Operating Grant: Clinical Trials Projects - Indirect Costs
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
474606
Name
Smaill Fiona M
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Infection and Immunity
Theme2
Biomedical
Prcname2
Operating Grant : Clinical Trials Projects
Projecttitle
A phase 2 trial to evaluate safety and immunogenicity of a next-generation COVID-19 vaccine delivered by inhaled aerosol to humans
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$2,066,579
Cihrequipment2
$0
Programname2
Operating Grant: Clinical Trials Projects - Indirect Costs
Keyworddelim
Adenoviral-Vectored; Antibody & T Cell Immunity; Clinical Trial; Covid-19; Inhaled Aerosol; Mucosal Immunization; Next-Generation Vaccine; Respiratory Mucosal Immunity; Sars-Cov2; Trained Innate Immunity
Abstract
Despite the benefit of current COVID vaccines in preventing severe disease and death, these vaccines are relatively poor at preventing infection with new variants like Omicron and work less well in the elderly and people with weak immune systems. There is an urgent need to develop new, next generation vaccines. As leaders in respiratory mucosal immunity, we have shown how delivering a vaccine directly to the lung by inhalation leads to better protection from infection than an IM injection. Before COVID, we were studying a new viral-vectored vaccine for TB inhaled into the lungs in healthy volunteers. We showed that this vaccine was safe and that good immune responses to TB were made in the lungs.
With the arrival of COVID, we developed next generation multivalent COVID-19 vaccines active against not only the spike protein but also internal viral proteins that do not mutate, even in variants. After showing that these vaccines were safe and protected against COVID infection in animals, we began a human trial with 30 healthy persons who had at least 2 doses of a mRNA vaccine and are studying in detail the immune responses in the lung and blood.
In our planned placebo-controlled Phase 2 study, we will enroll 500 participants from at least 3 clinical trial sites across Canada, to get more confidence in the safety of the inhaled route of administration and make the results more generalizable by enrolling older persons and those with underlying health conditions. We will gather safety and measures of immune responses to support a phase 3 clinical trial, with the goal of licensing and marketing our made-in-Canada vaccine and the aerosol method of administration. We expect this vaccine approach to be effective in breaking the cycle of new variant, poor vaccine performance, transmission and infection. The research team is led by Dr Fiona Smaill and includes members with a rich experience in vaccine clinical trials, vaccine manufacturing, aerosol delivery, and immunology.
Competitiondate
202207
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Smaill, Fiona M; Comeau, Jeannette L; Gauvreau, Gail M; Halperin, Scott A; Langley, Joanne M; Loeb, Mark B; Miller, Matthew S; Satia, Imran; Wang, Jun; Xing, Zhou
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $2,066,579~ $0~