CombiVacS: Vaccination With COMIRNATY in Subjects With a VAXZEVRIA First Dose
Study Details
Study Description
Brief Summary
CombiVacS is a phase 2 randomized, adaptive trial developed to evaluate the immunogenicity of a dose of COMIRNATY after a previous single dose of VAXZEVRIA. A stratification will be made based on the following factors: study site, sex and age. This protocol allows to test the immunogenicity and safety of a heterologous vaccination strategy after a previous single dose of VAXZEVRIA.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Detailed Description
This is a randomized, non-blinded, controlled, adaptive, multicenter, Phase II study in subjects aged ≥18 years and in good health or stable clinical situation that have received a previous single dose of VAXZEVRIA. Subjects will be randomized to immediately receive or not a dose of COMIRNATY in a ratio of 2:1. If primary analysis at day 14th confirms the starting hypothesis, subjects randomized to no vaccination will be considered for administration of one dose of COMINARTY at day 28th according to Public Health Department of the Ministry of Health recommendations on heterologous vaccination. In case the primary analysis does not confirm the starting hypothesis, subjects will be followed at the time points defined in the flow-chart without administration of COMIRNATY.
Other heterologous vaccination strategies could be incorporated if deemed necessary for public health reasons. This could include the use of different vaccination strategies including those already marketed vaccines for comparative assessment of their safety and efficacy on SARS-CoV-2 and its variants.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: VACCINATION One standard dose of COMIRNATY in adult subjects (18 years old) having received prior VAXZEVRIA vaccination. |
Drug: COMIRNATY
One dose of COMIRNATY
Other Names:
|
| No Intervention: NO INTERVENTION No vaccination in adult subjects (18 years old) having received prior VAXZEVRIA vaccination. If primary analysis at day 14th confirms the starting hypothesis, subjects randomized to this arm will be considered for administration of one dose of COMINARTY at day 28th according to Public Health Department of the Ministry of Health recommendations on heterologous vaccination. |
Outcome Measures
Primary Outcome Measures
- To assess the humoral immune response against SARS-CoV-2, 14 days after vaccination with COMIRNATY in subjects that received a previous single dose of VAXZEVRIA, as compared with no dosing. [14 days after randomization]
Antibodies against SARS-CoV-2 spike protein. Measure: BAU/mL
Secondary Outcome Measures
- To assess the humoral immune response against SARS-CoV-2, 28 days after vaccination with COMIRNATY in subjects that received a previous single dose of VAXZEVRIA. [28 days after randomization]
Antibodies against SARS-CoV-2 spike protein. Measure: BAU/mL
- To assess the long-term (up to 1 year) humoral immune response against SARS-CoV-2 of a dose of COMIRNATY in subjects that received a previous single dose of VAXZEVRIA. [3, 6 and 12 months after randomization]
Antibodies against SARS-CoV-2 spike protein (BAU/mL)
- To assess the occurrence of symptomatic molecularly confirmed COVID-19 and severity of COVID-19 signs and symptoms after the administration of a dose of COMIRNATY in subjects that received a prior single dose of VAXZEVRIA. [Month 1 - 12]
Number of participants with molecularly confirmed COVID-19 and presence and severity of COVID-19 signs and symptoms as measured by Symptoms of Infection with Coronavirus-19
- To evaluate the safety of a dose of COMIRNATY in subjects that received a previous single dose of VAXZEVRIA (solicited adverse events) [Day 1-7]
Number of solicited local and systemic adverse events (AEs) for 7 days after vaccine
- To evaluate the safety of a dose of COMIRNATY in subjects that received a previous single dose of VAXZEVRIA (unsolicited adverse events) [Day 1-28]
Number of unsolicited local and systemic adverse events (AEs) for 28 days after vaccine
- To evaluate the safety of a dose of COMIRNATY in subjects that received a previous single dose of VAXZEVRIA (serious adverse events) [Month 1-12]
Number of Serious adverse events (SAEs) throughout the study (from randomization until end of the study).
- To evaluate the safety of a dose of COMIRNATY in subjects that received a previous single dose of VAXZEVRIA (Medically-attended adverse events) [Month 1-6]
Number of Medically-attended adverse events (MAAEs) from the day of vaccination until 6 months after the last vaccination
Other Outcome Measures
- To evaluate the relationship between the immune response measured as NAV (Neutralizing antibodies) and antibodies against SARS-CoV-2 spike protein measured by immunoassay. [Month 1-12]
Neutralizing antibodies (BAU/mL) and antibodies against SARS-CoV-2 spike protein (BAU/mL)
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Adult subjects (18 years old) having received a prime VAXZEVRIA vaccination between 8 and 12 weeks before the screening visit
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Participants must provide consent indicating that he or she understands the purpose, procedures and potential risks and benefits of the study, and is willing to participate in the study.
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Subjects in good health or stable clinical situation.
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Participant is willing and able to adhere to the procedures specified in this protocol.
Exclusion Criteria:
-
Participant has a clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºC within 24 hours prior to the planned dose of study vaccine.
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Participant has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to COMIRNATY excipients.
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Subjects with any contraindication to the administration of COMIRNATY, included pregnancy.
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Subjects with prior documented COVID19 since VAXZEVRIA vaccination.
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Subjects have symptoms or signs compatible with COVID19.
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Subjects participating in a clinical trial in the last three months.
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Any condition or situation precluding or interfering the compliance with the protocol.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hospital Universitario de Cruces | Baracaldo | Bizkaia | Spain | 48903 |
| 2 | Hospital Vall d´Hebron | Barcelona | Spain | 08035 | |
| 3 | Hospital Clinic de Barcelona | Barcelona | Spain | 08036 | |
| 4 | Hospital Clínico San Carlos | Madrid | Spain | 28040 | |
| 5 | Hospital Universitario La Paz | Madrid | Spain | 28046 |
Sponsors and Collaborators
- Instituto de Investigación Hospital Universitario La Paz
- Instituto de Salud Carlos III
- Spanish Clinical Research Network - SCReN
Investigators
- Study Chair: Cristobal Belda Iniesta, MD, PhD, Instituto de Salud Carlos III
- Principal Investigator: Jesús Frías Iniesta, MD, PhD, Spanish Clinical Research Network - SCReN
- Study Director: Jose R Arribas, MD, PhD, Hospital Universitario La Paz
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 5859
- NCT04860739