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A Phase 3b/4 Randomised Trial of 3 Doses of Protein-based Covid-19 Vaccine (SpikoGen)

Primary Purpose

COVID-19

Status
Active
Phase
Phase 3
Locations
Australia
Study Type
Interventional
Intervention
Advax-CpG55.2 adjuvanted recombinant spike protein
Sponsored by
Vaxine Pty Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for COVID-19 focused on measuring sars-cov-2, coronavirus, vaccine, adjuvant, Advax, Spikogen, Covax-19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Able to provide written informed consent
  • Males or females* 18 years of age or older
  • Understand and are likely to comply with planned study procedures and be available for all study visits.
  • Have not previously had a Covid-19 vaccine and do not intend to have a non-study Covid-19 vaccine within the next 6 months

Exclusion Criteria:

  • History of Covid-19 vaccination.
  • History of serious vaccine allergy.
  • Pregnancy1
  • Have received an experimental agent within 30 days prior to the study vaccination or expect to receive another experimental agent during the trial reporting period.
  • Any medical, social or mental condition which, in the opinion of the investigator, would be detrimental to the subjects or the study.

Sites / Locations

  • ARASMI

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Spikogen vaccine - accelerated arm

Spikogen vaccine - standard arm

Arm Description

Spikogen vaccine 25 micrograms by intramuscular injection on study months 0, 1 and 2

Spikogen vaccine 25 micrograms by intramuscular injection on study months 0, 1 and 4

Outcomes

Primary Outcome Measures

First dose Seroconversion
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Second dose Seroconversion
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Third Dose Seroconversion
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Final Seroconversion
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
First Dose GMT
Spike protein antibody Geometric Mean Titers (GMT) in each group stratified by baseline antibody positivity
Second Dose GMT
Spike protein antibody Geometric Mean Titers (GMT) in each group stratified by baseline antibody positivity
Third Dose GMT
Spike protein antibody Geometric Mean Titers (GMT)in each group stratified by baseline antibody positivity
Final GMT
Spike protein antibody Geometric Mean Titers (GMT)in each group stratified by baseline antibody positivity
First Dose Adverse events (AE)
AE occurring within 7 days of immunisation in each group stratified by baseline antibody positivity
Second Dose Adverse events (AE)
AE occurring within 7 days of immunisation in each group stratified by baseline antibody positivity
Third Dose Adverse events (AE)
AE occurring within 7 days of immunisation in each group stratified by baseline antibody positivity
Serious adverse events (SAE)
Number of Serious adverse events (SAE) occurring within study period in each group stratified by baseline antibody positivity

Secondary Outcome Measures

First dose Vaccine efficacy
Proportion of Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Second dose Vaccine efficacy
Proportion of Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Third dose Vaccine efficacy
Proportion of Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Total Covid-19 infections
Proportion of breakthrough Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Seroconversion against variants of concern
Serum spike protein antibody seroconversion rates against each SARS-CoV-2 variant of concern in trial participants in each group stratified by baseline antibody positivity
GMT against variants of concern
Geometric mean serum spike protein antibodies against SARS-CoV-2 variants in trial participants in each group stratified by baseline antibody positivity

Full Information

First Posted
March 7, 2022
Last Updated
August 24, 2023
Sponsor
Vaxine Pty Ltd
Collaborators
Australian Respiratory and Sleep Medicine Institute
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1. Study Identification

Unique Protocol Identification Number
NCT05279456
Brief Title
A Phase 3b/4 Randomised Trial of 3 Doses of Protein-based Covid-19 Vaccine (SpikoGen)
Official Title
A Phase 3b/4 Randomised Trial of 3 Doses of Protein-based Covid-19 Vaccine (SpikoGen)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 15, 2022 (Actual)
Primary Completion Date
August 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Vaxine Pty Ltd
Collaborators
Australian Respiratory and Sleep Medicine Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will determine the immunogenicity of Spikogen in vaccine naïve individuals. Spikogen will be administered as two doses 1 month apart with a third booster dose either 1 or 3 months after the second dose. This study will provide key data on SARS-CoV-2 antibody responses.
Detailed Description
The SARS-CoV-2 outbreak has caused millions of deaths globally. It has a particularly high mortality rate in elderly people and those with chronic disease where mortality rates can be as high as 20-30%. SARS-COV-2 vaccines remain a key priority to help fight the current pandemic. COVID-19 vaccines prevent symptomatic infection and may help reduce virus transmission. Spikogen® vaccine, also known as Covax-19™ in Australia, is an adjuvanted recombinant protein Covid-19 vaccine has recently been approved by the Iranian FDA for emergency use in Iran in adults as a primary vaccine course and booster dose, after meeting its primary efficacy endpoint in a Phase 3 trial in 16,876 participants randomised 3:1 to receive Spikogen vaccine or saline placebo via two intramuscular doses 3 weeks apart where Spikogen vaccine demonstrated significant protection against serious infection with the delta variant. Approximately 5-10% of the broader Australian population and an even higher proportion of the indigenous populations remains unvaccinated despite current availability of these vaccines. One reason is that some people have medical contraindications to the current vaccines, such as serious allergies to the vaccine components such as polyethyleneglycol (PEG) in the mRNA vaccines. Spikogen vaccine is made using a recombinant protein approach with the SARS-CoV-2 spike protein synthesized in an insect cell line grown in broth. Insect cell expression of recombinant protein is a well-established vaccine manufacturing approach. Spikogen vaccine also contains a unique Australian developed adjuvant called Advax-CpG55.2, which is added to the spike protein to make the vaccine more effective. AdvaxCpG55.2 has two components, one a natural plant sugar called inulin, and the second a short synthetic oligonucleotide polymer, known as CpG55.2 oligonucleotide. Spikogen vaccine is designed to protect against SARS-CoV-2 infection. It has been shown to be effective against infection in hamster, ferret and monkey SARS-CoV-2 infection models. This study will determine the immunogenicity of Spikogen in vaccine-naïve individuals. Spikogen will be administered as two doses 31 month apart with a third booster dose given either 1 or 3 months after the second dose.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COVID-19
Keywords
sars-cov-2, coronavirus, vaccine, adjuvant, Advax, Spikogen, Covax-19

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Subjects will be stratified for analysis by age, sex and seropositivity at time of study entry
Masking
None (Open Label)
Allocation
Randomized
Enrollment
39 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Spikogen vaccine - accelerated arm
Arm Type
Experimental
Arm Description
Spikogen vaccine 25 micrograms by intramuscular injection on study months 0, 1 and 2
Arm Title
Spikogen vaccine - standard arm
Arm Type
Experimental
Arm Description
Spikogen vaccine 25 micrograms by intramuscular injection on study months 0, 1 and 4
Intervention Type
Biological
Intervention Name(s)
Advax-CpG55.2 adjuvanted recombinant spike protein
Other Intervention Name(s)
Spikogen vaccine
Intervention Description
recombinant SARS-CoV-2 spike protein formulated with Advax-CpG55.2 adjuvant
Primary Outcome Measure Information:
Title
First dose Seroconversion
Description
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Time Frame
2-4 weeks post first immunisation
Title
Second dose Seroconversion
Description
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Time Frame
2-4 weeks post second immunisation
Title
Third Dose Seroconversion
Description
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Time Frame
2-4 weeks post third immunisation
Title
Final Seroconversion
Description
Proportion of subjects in each group stratified by baseline antibody positivity seroconverting to spike protein antibody positivity
Time Frame
through study completion, an average of 7 months
Title
First Dose GMT
Description
Spike protein antibody Geometric Mean Titers (GMT) in each group stratified by baseline antibody positivity
Time Frame
2-4 weeks post first immunisation
Title
Second Dose GMT
Description
Spike protein antibody Geometric Mean Titers (GMT) in each group stratified by baseline antibody positivity
Time Frame
2-4 weeks post second immunisation
Title
Third Dose GMT
Description
Spike protein antibody Geometric Mean Titers (GMT)in each group stratified by baseline antibody positivity
Time Frame
2-4 weeks post third immunisation
Title
Final GMT
Description
Spike protein antibody Geometric Mean Titers (GMT)in each group stratified by baseline antibody positivity
Time Frame
through study completion, an average of 7 months
Title
First Dose Adverse events (AE)
Description
AE occurring within 7 days of immunisation in each group stratified by baseline antibody positivity
Time Frame
7 days post first immunisation
Title
Second Dose Adverse events (AE)
Description
AE occurring within 7 days of immunisation in each group stratified by baseline antibody positivity
Time Frame
7 days post second immunisation
Title
Third Dose Adverse events (AE)
Description
AE occurring within 7 days of immunisation in each group stratified by baseline antibody positivity
Time Frame
7 days post third immunisation
Title
Serious adverse events (SAE)
Description
Number of Serious adverse events (SAE) occurring within study period in each group stratified by baseline antibody positivity
Time Frame
through study completion, an average of 7 months
Secondary Outcome Measure Information:
Title
First dose Vaccine efficacy
Description
Proportion of Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Time Frame
From 2 weeks post-first dose to 2 weeks after second dose
Title
Second dose Vaccine efficacy
Description
Proportion of Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Time Frame
From 2 weeks post-second dose to 2 weeks after third dose
Title
Third dose Vaccine efficacy
Description
Proportion of Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Time Frame
From 2 weeks post-third dose through study completion, an average of 7 months
Title
Total Covid-19 infections
Description
Proportion of breakthrough Covid-19 infections in trial participants in each group stratified by baseline antibody positivity
Time Frame
From first vaccine dose through study completion, an average of 7 months
Title
Seroconversion against variants of concern
Description
Serum spike protein antibody seroconversion rates against each SARS-CoV-2 variant of concern in trial participants in each group stratified by baseline antibody positivity
Time Frame
2-4 weeks post first, second and third immunisation and at study completion
Title
GMT against variants of concern
Description
Geometric mean serum spike protein antibodies against SARS-CoV-2 variants in trial participants in each group stratified by baseline antibody positivity
Time Frame
2-4 weeks post first, second and third immunisation and at study completion
Other Pre-specified Outcome Measures:
Title
Antibody kinetics
Description
rate of change in peak to trough serum spike protein antibody levels over time in each group stratified by baseline antibody positivity
Time Frame
2-4 weeks post first, second and third immunisation and at study completion
Title
Age effects on seroconversion
Description
Proprotion seroconverting to spike protein antibodies analysed by age and gender
Time Frame
2-4 weeks post first, second and third immunisation and at study completion
Title
Age effects on antibody levels
Description
Geometric Mean Titers of spike protein antibodies in participants by age and gender
Time Frame
2-4 weeks post first, second and third immunisation and at study completion
Title
immune-deficiency effects on seroconversion
Description
Proportion of subjects seroconverting to spike protein antibodies in participants with or without immune-deficiency
Time Frame
2-4 weeks post first, second and third immunisation and at study completion
Title
immune-deficiency effects on antibody levels
Description
Geometric Mean Titers (GMT) of spike protein antibodies in participants with or without immune-deficiency
Time Frame
2-4 weeks post first, second and third immunisation and at study completion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Able to provide written informed consent Males or females* 18 years of age or older Understand and are likely to comply with planned study procedures and be available for all study visits. Have not previously had a Covid-19 vaccine and do not intend to have a non-study Covid-19 vaccine within the next 6 months Exclusion Criteria: History of Covid-19 vaccination. History of serious vaccine allergy. Pregnancy1 Have received an experimental agent within 30 days prior to the study vaccination or expect to receive another experimental agent during the trial reporting period. Any medical, social or mental condition which, in the opinion of the investigator, would be detrimental to the subjects or the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dimitar Sajkov, MBBS
Organizational Affiliation
ARASMI
Official's Role
Study Director
Facility Information:
Facility Name
ARASMI
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5042
Country
Australia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no current plan to share IPD with other researchers, but requests for data access will be considered on a case by case basis
Citations:
PubMed Identifier
34420786
Citation
Li L, Honda-Okubo Y, Huang Y, Jang H, Carlock MA, Baldwin J, Piplani S, Bebin-Blackwell AG, Forgacs D, Sakamoto K, Stella A, Turville S, Chataway T, Colella A, Triccas J, Ross TM, Petrovsky N. Immunisation of ferrets and mice with recombinant SARS-CoV-2 spike protein formulated with Advax-SM adjuvant protects against COVID-19 infection. Vaccine. 2021 Sep 24;39(40):5940-5953. doi: 10.1016/j.vaccine.2021.07.087. Epub 2021 Aug 3.
Results Reference
background
Links:
URL
http://vaxine.net
Description
Link to company website

Learn more about this trial

A Phase 3b/4 Randomised Trial of 3 Doses of Protein-based Covid-19 Vaccine (SpikoGen)

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