Study of a Combination SARS-CoV-2 Recombinant Spike and High-Dose Inactivated Influenza Vaccine With Matrix-M Adjuvant in Adult Participants 60 Years of Age and Older
A Phase 3, Parallel, Randomized, Modified Double-Blind, Active-Controlled, Multi-Arm Study to Assess the Safety and Immunogenicity of a Combination Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Recombinant Spike and High-Dose Inactivated Influenza Vaccine With Matrix-M Adjuvant in Adult Participants 60 Years of Age and Older
The purpose of this study is to assess the safety and immunogenicity of IIV-HD + NVXC19 vaccine compared to seasonal influenza vaccine (IIV-HD) and COVID-19 vaccine, adjuvanted (NVXC19) coadministered in adult participants 60 years of age and older. Placebo will be coadministered in the IIV-HD + NVXC19 study group to control for the number of injections and to maintain observer-blinding. Thus, each participant will receive 2 injections at enrollment, one in each deltoid muscle.
Study details include:
- The study duration will be approximately 12 months per participant
- Study intervention will be administered via a single IM injection into the right and left deltoid muscles on day (D)01
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 3
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Trial Transparency email recommended (Toll free for US & Canada)
- Telefonnummer: option 6 800-633-1610
- E-mail: Contact-US@sanofi.com
Studiesteder
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Lower Silesian Voivodeship
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Wroclaw, Lower Silesian Voivodeship, Polen, 50-088
- Rekruttering
- Investigational Site Number : 6160002
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Pomeranian Voivodeship
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Gdynia, Pomeranian Voivodeship, Polen, 81-384
- Rekruttering
- Investigational Site Number : 6160020
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion criteria
Inclusion criteria to be checked at Screening Visit:
- Aged 60 years or older on the day of inclusion
- Informed consent form has been signed and dated
- Able to attend all scheduled visits and to comply with all study procedures
- Participant must be able to receive an injection in the deltoid muscle of both arms
- Participant must have completed a primary vaccination series against SARS-CoV-2 and at least 1 booster with a locally authorized or approved COVID-19 vaccine Inclusion criteria to be checked at Visit 1 (D01)
- Aged 60 years or older on the day of inclusion
- Participants who are healthy or with pre-existing stable condition, as determined by medical evaluation including medical history and physical examination
- Non-childbearing potential (i.e., post-menopausal for at least 1 year or surgically sterile)
- lnformed consent form has been signed and dated
- Able to attend all scheduled visits and to comply with all study procedures
- Participant must be able to receive an injection in the deltoid muscle of both arms
- Participant must have completed a primary vaccination series against SARS-CoV-2 and at least 1 booster with a locally authorized or approved COVID-19 vaccine
Exclusion criteria Exclusion Criteria to be Checked at Screening Visit and at Visit 1 (D01) Medical conditions
- Known/suspected immunodeficiency; immunosuppressive therapy in past 6 months; long-term systemic corticosteroids
- Known systemic hypersensitivity to any study intervention components or history of life-threatening reaction to study interventions or products with the same substances
- Self-reported thrombocytopenia, contraindicating intramuscular injection, based on investigator's judgment
- Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion, contraindicating intramuscular injection, based on investigator's judgment
- Chronic illness that, in the opinion of the investigator, is at a stage where it might interfere with study conduct or completion
- Moderate/severe acute illness/infection (per investigator judgment)/fever (≥38.0°C [≥100.4°F]) on study intervention day. Include participant only after the condition or fever has resolved.
- Alcohol, prescription drug, or substance abuse that, in the opinion of the Investigator, might interfere with the study conduct or completion
- History of serious adverse reaction to any influenza or COVID-19 vaccines per investigator's judgment
- Personal or family history of Guillain-Barré syndrome
- Prior history of myocarditis, pericarditis, or myopericarditis Prior/concomitant therapy
- Any vaccine given within 4 weeks before or within 4 weeks after study intervention
- Previous vaccination against influenza (in the previous 6 months before study intervention) with an investigational or marketed vaccine OR history of influenza infection in the previous 6 months
- Previous vaccination against COVID-19 (in the previous 6 months before study intervention) with an investigational or marketed vaccine OR history of COVID-19 infection in the previous 6 months
- Has received a blood transfusion or blood-derived products, including immunoglobulins, in the past 3 months Other exclusion
- Deprived of freedom by an administrative or court order, or being in an emergency setting, or hospitalized involuntarily
- Is an investigator, investigator/study center employee, or immediate family member (parent, spouse, natural/adopted child) of the investigator/employee with direct involvement in the study The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Tredobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Aktiv komparator: Group 1, IIV-HD and EU-licensed NVXC19
IIV-HD and NVXC19 co-administered in opposite deltoid muscles |
Pharmaceutical form: Suspension Route of administration: Intramuscular injection Pharmaceutical form: Dispersion Route of administration: Intramuscular injection |
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Eksperimentel: Group 2, IIV-HD + NVXC19 combination and placebo
IIV-HD + NVXC19 and Placebo co-administered in opposite deltoid muscles |
Pharmaceutical form: Suspension Route of administration: Intramuscular injection Pharmaceutical form: Solution Route of administration: Intramuscular injection |
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Antibody titers against for each of the 3 influenza vaccine strains(in a subset of participants)
Tidsramme: At Day 28 after vaccination
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Geometric mean (GMT) of antibody titers measured by hemagglutination inhibition (HAI) |
At Day 28 after vaccination
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Antibody titers against SARS-CoV-2 specific variant(in a subset of participants)
Tidsramme: At Day 28 after vaccination
|
Geometric mean (GMT) of antibody titers measured by pseudovirus neutralization test (PNT) |
At Day 28 after vaccination
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Presence of solicited injection site reactions for 8 days, including the day of vaccination (Main subset of participants)
Tidsramme: Up to 8 each days after vaccination
|
Number of participants with solicited injection site reactions pre-listed in the participant diary and case report form (CRF) |
Up to 8 each days after vaccination
|
|
Presence of solicited systemic reactions for 8 days, including the day of vaccination (Main subset of participants)
Tidsramme: Up to 8 each days after vaccination
|
Number of participants with solicited systemic reactions pre-listed in the participant diary and case report form (CRF) |
Up to 8 each days after vaccination
|
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Presence of immediate adverse events after vaccination
Tidsramme: Within the 30 minutes after vaccination
|
Number of participants with immediate adverse events (AEs). Immediate adverse events are any unsolicited systemic adverse events within 30 minutes after vaccination |
Within the 30 minutes after vaccination
|
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Presence of unsolicited adverse events
Tidsramme: Up to 28 days after vaccination
|
Number of participants with unsolicited adverse events (AEs) for 28 days, including the day of vaccination |
Up to 28 days after vaccination
|
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Presence of all medically attended adverse events
Tidsramme: Up to 180 days after vaccination
|
Number of participants with medical attended adverse events (MAAEs) for 180 days, including the day of vaccination |
Up to 180 days after vaccination
|
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Presence of related medically attended adverse events linked to predefined potential immune-mediated diseases
Tidsramme: From Day 181 through 12 months following study vaccination
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Number of participants with medical attended adverse events (MAAEs) linked to predefined potential immune-mediated diseases (PIMDs) following the study vaccination |
From Day 181 through 12 months following study vaccination
|
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Presence of all adverse events of special interest
Tidsramme: Up to 180 days after vaccination
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Number of participants with adverse events of special interest (AESIs) for 180 days, including the day of vaccination |
Up to 180 days after vaccination
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Presence of all serious adverse events
Tidsramme: Up to 180 days after vaccination
|
Number of participants with serious adverse events (SAEs) for 180 days, including the day of vaccination |
Up to 180 days after vaccination
|
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Presence of related serious adverse events
Tidsramme: From Day 181 through 12 months following study vaccination
|
Number of participants with serious adverse events (SAEs) from D181 through 12 months following the last study vaccination |
From Day 181 through 12 months following study vaccination
|
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Presence of related adverse events of special interest
Tidsramme: From Day 181 through 12 months following study vaccination
|
Number of participants with adverse events of special interest (AESIs) from D181 through 12 months following the last study vaccination |
From Day 181 through 12 months following study vaccination
|
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Presence of related medical attended adverse events linked to predefined potential immune-mediated diseases that meet the criteria for serious adverse events
Tidsramme: From Day 181 through 12 months following study vaccination
|
Number of patients with medical attended adverse events (MAAES) linked to predefined potential immune-mediated diseases (PIMDs) meets criteria for serious adverse events (SAEs) from D181 through 12 months following the last study vaccination |
From Day 181 through 12 months following study vaccination
|
|
Presence of adverse events leading to study discontinuation throughout the study
Tidsramme: From Day 01 through 12 months
|
Number of participants with adverse events lead to study discontinuation |
From Day 01 through 12 months
|
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Influenza seroconversion status after vaccination for each of the 3 influenza vaccine strains
Tidsramme: At Day 29
|
Percentage of participants Seroconversion is defined by: pre-injection antibody titer < 10 [1/dil] at D01 and post-injection antibody titer ≥ 40 [1/dil] at D29, or pre-injection antibody titer ≥ 10 [1/dil] at D01 and a ≥ 4-fold increase in titer at D29 |
At Day 29
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SARS-CoV-2 seroresponse status after vaccination
Tidsramme: At Day 29
|
Percentage of participantsSeroresponse to SARS-CoV-2 is defined by: pre-injection antibody titer < LLOQ [1/dil] and post-injection antibody titer ≥ 4*LLOQ [1/dil] at D29, or pre-injection antibody titer ≥ LLOQ [1/dil] at D01 and a ≥ 4-fold increase in titer [1/dil] at D29 |
At Day 29
|
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Neutralizing antibody titers measured by neutralization test (NT) against each of the 3 influenza vaccine strains before and after vaccination (in a subset of participants)
Tidsramme: At Day 01 and Day 29
|
Neutralizing antibody titers [1/dil] |
At Day 01 and Day 29
|
|
Individual neutralizing antibody titer ratio measured by neutralization test NT against each of the 3 influenza vaccine strains after vaccination (in a subset of participants)
Tidsramme: At Day 01 and Day 29
|
Individual neutralizing titers ratio Day 29/Day 01 |
At Day 01 and Day 29
|
|
Neutralizing antibody titer against each of the 3 influenza vaccine strains after vaccination(in a subset of participants)
Tidsramme: At Day 29
|
Percentage of participants with neutralization test (NT) titer ≥ 10 (1/dil) |
At Day 29
|
|
Neutralizing antibody titer against each of the 3 influenza vaccine strains after vaccination (in a subset of participants)
Tidsramme: At Day 29
|
Percentage of participants with neutralization test (NT) titer ≥ 20 (1/dil) |
At Day 29
|
|
Neutralizing antibody titer against each of the 3 influenza vaccine strains after vaccination (in a subset of participants)
Tidsramme: At Day 29
|
Percentage of participants with neutralization test (NT) titer ≥ 40 (1/dil) |
At Day 29
|
|
Neutralizing antibody titer against each of the 3 influenza vaccine strains after vaccination (in a subset of participants)
Tidsramme: At Day 29
|
Percentage of participants with neutralization test (NT) titer ≥ 80 (1/dil) |
At Day 29
|
|
Fold increase in neutralization test antibody titer against each of the 3 influenza vaccine strains after vaccination (in a subset of participants)
Tidsramme: At Day 29
|
Percentage of participants fold increase is defined in neutralization test (NT) antibody titer [post/pre] ≥ 2-fold rise from Day 01 to Day 29 |
At Day 29
|
|
Fold increase in neutralization test antibody titer against each of the 3 influenza vaccine strains after vaccination (in a subset of participants)
Tidsramme: At Day 29
|
Percentage of participants fold increase is defined in neutralization test (NT) antibody titer [post/pre] ≥ 4-fold rise from Day 01 to Day 29 |
At Day 29
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- VBT00004
- 2026-526221-18 (Registry Identifier: CTIS EU)
- U1111-1332-8880 (Registry Identifier: WHO)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
IPD-planbeskrivelse
Qualified researchers may request access to patient level data and related study documents including the clinical study report, study protocol with any amendments, blank case report form, statistical analysis plan, and dataset specifications. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Further details on Sanofi's data sharing criteria, eligible studies, and process for requesting access can be found at: https://vivli.org
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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