A Study to Evaluate the Safety and Immunogenicity of COVID-19 Vaccine and Influenza Combination Vaccine : A Randomized, Observer-Blinded, Active-Controlled Study to Evaluate the Safety and Immunogenicity of a SARS CoV 2 rS Nanoparticle and Trivalent Hemagglutinin Nanoparticle Influenza Combination Vaccine With Matrix-M™ Adjuvant in Participants ≥ 50 Years of Age
This is a randomized, observer-blinded, active-controlled Phase 3 study to demonstrate the noninferior immunogenicity of a coronavirus disease 2019 (COVID-19) and influenza combination (CIC) vaccine relative to age-appropriate licensed influenza vaccine comparators in terms of hemagglutinin inhibition (HAI) response and Novavax COVID-19 Vaccine in terms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) neutralizing antibody (NAb) response and to further evaluate the safety and immunogenicity of a CIC vaccine..
Medienart: |
Klinische Studie |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
ClinicalTrials.gov - (2024) vom: 20. März Zur Gesamtaufnahme - year:2024 |
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Sprache: |
Englisch |
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Links: |
Volltext [kostenfrei] |
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Themen: |
610 |
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Anmerkungen: |
Source: Link to the current ClinicalTrials.gov record., First posted: March 4, 2024, Last downloaded: ClinicalTrials.gov processed this data on March 27, 2024, Last updated: March 27, 2024 |
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Study ID: |
NCT06291857 |
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Veröffentlichungen zur Studie: |
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fisyears: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
CTG000074969 |
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245 | 1 | 0 | |a A Study to Evaluate the Safety and Immunogenicity of COVID-19 Vaccine and Influenza Combination Vaccine |b A Randomized, Observer-Blinded, Active-Controlled Study to Evaluate the Safety and Immunogenicity of a SARS CoV 2 rS Nanoparticle and Trivalent Hemagglutinin Nanoparticle Influenza Combination Vaccine With Matrix-M™ Adjuvant in Participants ≥ 50 Years of Age |
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520 | |a This is a randomized, observer-blinded, active-controlled Phase 3 study to demonstrate the noninferior immunogenicity of a coronavirus disease 2019 (COVID-19) and influenza combination (CIC) vaccine relative to age-appropriate licensed influenza vaccine comparators in terms of hemagglutinin inhibition (HAI) response and Novavax COVID-19 Vaccine in terms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) neutralizing antibody (NAb) response and to further evaluate the safety and immunogenicity of a CIC vaccine. | ||
650 | 2 | |a COVID-19 | |
650 | 2 | |a Influenza, Human | |
650 | 4 | |a Study Type: Interventional | |
650 | 4 | |a Recruitment Status: Not yet recruiting | |
650 | 4 | |a Phase: Phase 2, Phase 3 | |
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