Clinical Trials - NVAX

NCT IDTitleStatusPhasesStart DateCompletion DatePrimary Completion Date
NCT07086222Efficacy and Safety of NVX-CoV2705NOT_YET_RECRUITINGPHASE42025-11-102026-07-092026-01-09
NCT07079670Safety and Immunogenicity of NVX-CoV2705NOT_YET_RECRUITINGPHASE32025-10-162026-06-162026-04-16
NCT06482359Lot Consistency Study of COVID-19 and Influenza Combination VaccineWITHDRAWNPHASE2, PHASE32025-02-012026-05-172025-11-16
NCT06291857A Study to Evaluate the Safety and Immunogenicity of COVID-19 Vaccine and Influenza Combination VaccineACTIVE_NOT_RECRUITINGPHASE32024-12-092026-09-302026-07-26
NCT06485752Phase 3 Lot Consistency Study of Trivalent Hemagglutinin Nanoparticle Influenza VaccineWITHDRAWNPHASE2, PHASE32024-112025-02-042025-02-04
NCT06409663A Strain Change Study for SARS-CoV-2 rS VaccinesCOMPLETEDPHASE32024-10-142025-04-172024-10-15
NCT06633835Impact of Reactogenicity of the 2024-2025 COVID-19 Vaccines on Health Care Workers and First Responders in the United StatesACTIVE_NOT_RECRUITINGPHASE42024-09-202025-08-312025-06-30
NCT05925127Phase 2/3 Heterologous Boosting Study With Different Dose Levels of Monovalent SARS-CoV-2 rS VaccinesCOMPLETEDPHASE2, PHASE32023-10-162024-05-212024-05-21
NCT05975060A Study to Evaluate the Safety and Immunogenicity of an (Omicron Subvariant) COVID-19 Vaccine Booster Dose in Previously Vaccinated Participants and Unvaccinated Participants.COMPLETEDPHASE2, PHASE32023-09-072024-05-202023-11-15
NCT05973006Phase 3 Adolescent Study for SARS-CoV-2 rS Variant VaccinesCOMPLETEDPHASE32023-08-162024-09-302024-04-01
NCT05875701Phase 3 Study of Novavax Vaccine(s) as Booster Dose After mRNA VaccinesCOMPLETEDPHASE32023-03-282023-11-112023-11-11
NCT05519839A Study to Evaluate the Safety and Immunogenicity of COVID-19 and Influenza Combination VaccineCOMPLETEDPHASE22022-12-302023-12-242023-07-25
NCT05468736Study to Evaluate Safety and Immunogenicity of COVID-19 Vaccine in Children 6 Months to < 12 YearsACTIVE_NOT_RECRUITINGPHASE2, PHASE32022-07-222025-10-252024-01-16
NCT05463068Study to Compare the Immunogenicity and Safety of 3 Lots of NVX-CoV2373 in AdultsCOMPLETEDPHASE32022-07-112022-09-012022-08-17
NCT05372588Phase 3 Boosting Study for the SARS-CoV-2 rS Variant VaccinesCOMPLETEDPHASE32022-05-252024-04-072022-07-17
NCT05112848A Study to Evaluate Safety and Immunogenicity of a COVID-19 Vaccine in People Living With HIV at Risk for SARS-CoV-2 (COVID-19)COMPLETEDPHASE22022-02-282022-11-302022-05-23
NCT05029856Evaluation of the Safety and Immunogenicity of SII Vaccine Constructs Based on the SARS-CoV-2 (COVID-19) Variant in AdultsWITHDRAWNPHASE1, PHASE22022-02-042022-082022-08
NCT04961541Evaluation of the Safety and Immunogenicity of Influenza and COVID-19 Combination VaccineCOMPLETEDPHASE1, PHASE22021-09-082022-04-222021-12-22
NCT04611802A Study to Evaluate the Efficacy, Immune Response, and Safety of a COVID-19 Vaccine in Adults ≥ 18 Years With a Pediatric Expansion in Adolescents (12 to<18 Years) at Risk for SARS-CoV-2COMPLETEDPHASE32020-12-272023-12-152023-04-10
NCT04583995A Study Looking at the Effectiveness, Immune Response, and Safety of a COVID-19 Vaccine in Adults in the United KingdomCOMPLETEDPHASE32020-09-282022-03-292022-03-29
NCT04533399A Study Looking at the Effectiveness and Safety of a COVID-19 Vaccine in South African AdultsCOMPLETEDPHASE22020-08-172022-01-192021-12-07
NCT04368988Evaluation of the Safety and Immunogenicity of a SARS-CoV-2 rS Nanoparticle Vaccine With/Without Matrix-M AdjuvantCOMPLETEDPHASE1, PHASE22020-05-252022-06-012022-06-01
NCT04120194Phase 3 Pivotal Trial of NanoFluâ„¢ in Older AdultsCOMPLETEDPHASE32019-10-142020-12-132020-10-29
NCT03658629Phase 2 Dose and Formulation Confirmation of Quad-NIV in Older AdultsTERMINATEDPHASE22018-09-242019-04-262019-04-26
NCT03293498Evaluation of the Safety and Immunogenicity of a Recombinant Trivalent Nanoparticle Influenza Vaccine With Matrix M-1 Adjuvant (NanoFlu)COMPLETEDPHASE1, PHASE22017-09-182018-10-292018-03-14
NCT03026348Safety and Immunogenicity Study to Evaluate Single- or Two-Dose Regimens Of RSV F Vaccine With and Without Aluminum Phosphate or Matrix-M1â„¢ Adjuvants In Clinically-Stable Older AdultsCOMPLETEDPHASE22017-012018-05-182017-04
NCT02624947A Study to Determine the Safety and Efficacy of the RSV F Vaccine to Protect Infants Via Maternal ImmunizationCOMPLETEDPHASE32015-122019-07-122018-12-28
NCT02608502A Study to Evaluate the Efficacy of an RSV F Vaccine in Older AdultsCOMPLETEDPHASE32015-112016-122016-12
NCT02593071Safety and Immunogenicity of the RSV-F Vaccine in Older Adults Previously Treated With the Same Vaccine or Placebo in the Prior Year.COMPLETEDPHASE22015-102016-112016-11
NCT02370589Study to Evaluate the Immunogenicity and Safety of an Ebola Virus (EBOV) Glycoprotein (GP) Vaccine in Healthy SubjectsCOMPLETEDPHASE12015-022016-042016-04
NCT02307851Quadrivalent Influenza VLP Vaccine Dose Ranging Study in Young AdultsCOMPLETEDPHASE22014-112015-062015-06
NCT02296463A Phase I Randomized, Observer-Blinded, Dose-Ranging Study in Healthy Subjects 24 to <72 Months of AgeCOMPLETEDPHASE12014-112016-042015-09
NCT02266628Placebo- Controlled Study to Evaluate the Safety and Immunogenicity of the RSV-F Vaccine in Elderly AdultsCOMPLETEDPHASE22014-102016-032016-03
NCT02247726RSV F Vaccine Maternal Immunization Study in Healthy Third-trimester Pregnant Women.COMPLETEDPHASE22014-092016-072016-07
NCT02078674A(H7N9) VLP Antigen Dose-Ranging Study With Matrix-M1â„¢ AdjuvantCOMPLETEDPHASE1, PHASE22014-032015-072015-07
NCT01960686RSV F Dose-Ranging Study in WomenCOMPLETEDPHASE22013-102014-042014-04
NCT01897701A(H7N9) VLP Antigen Dose Ranging Study With Adjuvant 1COMPLETEDPHASE12013-072014-082014-08
NCT01709019RSV-F Vaccine and Influenza Vaccine Co-Administration Study in the ElderlyCOMPLETEDPHASE12012-102014-032013-07
NCT01704365RSV-F Vaccine Dose Ranging Study in Young WomenCOMPLETEDPHASE22012-102013-052013-04
NCT01596725A/H5N1 Virus-Like Particle Antigen Dose Ranging Study With Adjuvant 2COMPLETEDPHASE12012-052013-082012-08
NCT01594320A/H5N1 Virus-Like Particle Antigen Dose Ranging Study With Adjuvant 1COMPLETEDPHASE12012-042013-082012-07
NCT01561768A Study to Evaluate the Immune Response and Safety of a Seasonal Virus-Like Particle Influenza Vaccine in Healthy Young AdultsCOMPLETEDPHASE22012-032013-012013-01
NCT01290419Safety Study of Respiratory Syncytial Virus (RSV)-Fusion (F) Protein Particle VaccineCOMPLETEDPHASE12010-122011-122011-12
NCT01014806Evaluate the Safety and Immunogenicity of a Seasonal Influenza Virus-Like Particle (VLP) Vaccine in Older AdultsCOMPLETEDPHASE22009-112010-052010-05
NCT01072799Safety and Immunogenicity of an A (H1N1) 2009 Influenza Virus-like Particle (VLP) VaccineCOMPLETEDPHASE22009-102012-032012-03
NCT00903552Trial to Evaluate Safety and Immunogenicity of Trivalent Seasonal Influenza Virus-Like Particle (VLP) Vaccine (Recombinant)COMPLETEDPHASE22009-052009-102009-10
NCT00754455Evaluate the Safety and Immunogenicity of a Seasonal Influenza VLP Vaccine (Recombinant) in Healthy AdultsCOMPLETEDPHASE22008-092009-032009-03
NCT00519389Safety, Reactogenicity and Immunogenicity of an H5N1 VLPCOMPLETEDPHASE1, PHASE22007-072008-112008-11