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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

maanantai 9. marraskuuta 2026 päivittänyt: Sanofi

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

Tutkimuksen yleiskatsaus

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

6000

Vaihe

  • Vaihe 3

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

  • Nimi: Trial Transparency email recommended (Toll free for US & Canada)
  • Puhelinnumero: option 6 800-633-1610
  • Sähköposti: Contact-US@sanofi.com

Opiskelupaikat

    • Lower Silesian Voivodeship
      • Wroclaw, Lower Silesian Voivodeship, Puola, 50-088
        • Rekrytointi
        • Investigational Site Number : 6160002
    • Pomeranian Voivodeship
      • Gdynia, Pomeranian Voivodeship, Puola, 81-384
        • Rekrytointi
        • Investigational Site Number : 6160020

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

60 vuotta ja vanhemmat (Aikuinen, Vanhempi Aikuinen)

Hyväksyy terveitä vapaaehtoisia

Joo

Sukupuolet, jotka voivat opiskella

Kaikki

Kuvaus

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

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Ennaltaehkäisy
  • Jako: Satunnaistettu
  • Inventiomalli: Rinnakkaistehtävä
  • Naamiointi: Kolminkertaistaa

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Active Comparator: 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

Kokeellinen: 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

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Antibody titers against for each of the 3 influenza vaccine strains(in a subset of participants)
Aikaikkuna: At Day 28 after vaccination

Geometric mean (GMT) of antibody titers measured by hemagglutination inhibition (HAI)

At Day 28 after vaccination
Antibody titers against SARS-CoV-2 specific variant(in a subset of participants)
Aikaikkuna: At Day 28 after vaccination

Geometric mean (GMT) of antibody titers measured by pseudovirus neutralization test (PNT)

At Day 28 after vaccination

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Presence of solicited injection site reactions for 8 days, including the day of vaccination (Main subset of participants)
Aikaikkuna: 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)
Aikaikkuna: 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
Presence of immediate adverse events after vaccination
Aikaikkuna: 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
Presence of unsolicited adverse events
Aikaikkuna: 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
Presence of all medically attended adverse events
Aikaikkuna: 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
Presence of related medically attended adverse events linked to predefined potential immune-mediated diseases
Aikaikkuna: From Day 181 through 12 months following study vaccination

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
Presence of all adverse events of special interest
Aikaikkuna: Up to 180 days after vaccination

Number of participants with adverse events of special interest (AESIs) for 180 days, including the day of vaccination

Up to 180 days after vaccination
Presence of all serious adverse events
Aikaikkuna: 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
Presence of related serious adverse events
Aikaikkuna: 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
Presence of related adverse events of special interest
Aikaikkuna: 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
Presence of related medical attended adverse events linked to predefined potential immune-mediated diseases that meet the criteria for serious adverse events
Aikaikkuna: 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
Aikaikkuna: From Day 01 through 12 months

Number of participants with adverse events lead to study discontinuation

From Day 01 through 12 months
Influenza seroconversion status after vaccination for each of the 3 influenza vaccine strains
Aikaikkuna: 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
SARS-CoV-2 seroresponse status after vaccination
Aikaikkuna: 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
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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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)
Aikaikkuna: 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

Yhteistyökumppanit ja tutkijat

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Sponsori

Julkaisuja ja hyödyllisiä linkkejä

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Hyödyllisiä linkkejä

Opintojen ennätyspäivät

Nämä päivämäärät seuraavat ClinicalTrials.gov-sivustolle lähetettyjen tutkimustietueiden ja yhteenvetojen edistymistä. National Library of Medicine (NLM) tarkistaa tutkimustiedot ja raportoidut tulokset varmistaakseen, että ne täyttävät tietyt laadunvalvontastandardit, ennen kuin ne julkaistaan ​​julkisella verkkosivustolla.

Opi tärkeimmät päivämäärät

Opiskelun aloitus (Todellinen)

Keskiviikko 28. lokakuuta 2026

Ensisijainen valmistuminen (Arvioitu)

Tiistai 28. joulukuuta 2027

Opintojen valmistuminen (Arvioitu)

Tiistai 28. joulukuuta 2027

Opintoihin ilmoittautumispäivät

Ensimmäinen lähetetty

Torstai 15. lokakuuta 2026

Ensimmäinen toimitettu, joka täytti QC-kriteerit

Torstai 15. lokakuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Torstai 22. lokakuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Perjantai 13. marraskuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

Maanantai 9. marraskuuta 2026

Viimeksi vahvistettu

Sunnuntai 1. marraskuuta 2026

Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muut tutkimustunnusnumerot

  • VBT00004
  • 2026-526221-18 (Rekisterin tunniste: CTIS EU)
  • U1111-1332-8880 (Rekisterin tunniste: WHO)

Yksittäisten osallistujien tietojen suunnitelma (IPD)

Aiotko jakaa yksittäisten osallistujien tietoja (IPD)?

JOO

IPD-suunnitelman kuvaus

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

Lääke- ja laitetiedot, tutkimusasiakirjat

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Ei

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Ei

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