Evaluation of the Safety and Immunogenicity of a SARS-CoV-2 rS Nanoparticle Vaccine With/Without Matrix-M Adjuvant

COVID-19 Clinical Trial

Official title:

A 2-Part, Phase 1/2, Randomized, Observer-Blinded Study To Evaluate The Safety And Immunogenicity Of A SARS-CoV-2 Recombinant Spike Protein Nanoparticle Vaccine (SARS-CoV-2 rS) With Or Without MATRIX-M™ Adjuvant In Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04368988
• Other study ID #: 2019nCoV-101
• Status: Completed
• Phase: Phase 1/Phase 2
• Start date: May 25, 2020
• Est. completion date: June 1, 2022

Study information

• Verified date: April 2023
• Source: Novavax
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

2019nCoV-101 is a 2-part, randomized, observer-blinded, placebo-controlled, Phase 1/2 trial. Part 1 (Phase 1) of the study is designed to evaluate the safety and immunogenicity of SARS-CoV-2 rS nanoparticle vaccine with or without Matrix-M adjuvant in 131 healthy participants ≥ 18 to 59 (inclusive) years of age at 2 sites in Australia. An interim analysis of Part 1 safety and immunogenicity will be performed prior to optional expansion to Part 2. Part 2 (Phase 2) of the study is designed to evaluate the immunogenicity, safety, and preliminary efficacy of a single construct of SARS-CoV-2 rS nanoparticle vaccine with Matrix-M adjuvant in up to 1,500 healthy participants ≥ 18 to 84 (inclusive) years of age at up to 40 sites across Australia and/or the United States.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1419
• Est. completion date: June 1, 2022
• Est. primary completion date: June 1, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 84 Years

Eligibility

Inclusion Criteria (Part 1):

• Healthy adult males or females between 18 and 59 years of age, inclusive, at screening. Healthy status will be determined by the investigator based on medical history, clinical laboratory results, vital sign measurements, and physical examination at screening.

• The participant has a body mass index 17 to 35 kg/m2, inclusive, at screening.

• Willing and able to give informed consent prior to study enrollment and comply with study procedures.

• Female participants of childbearing potential (defined as any female who has experienced menarche and who is NOT surgically sterile [ie, hysterectomy, bilateral tubal ligation, or bilateral oophorectomy] or postmenopausal [defined as amenorrhea at least 12 consecutive months or documented plasma follicle-stimulating hormone (FSH) level =40 mIU/mL]) must agree to be heterosexually inactive from at least 21 days prior to enrollment and through 6 months after the last vaccination OR agree to consistently use any of the described methods of contraception from at least 21 days prior to enrollment and through 6 months after the last vaccination.

Exclusion Criteria (Part 1):

• Any ongoing, symptomatic acute or chronic illness requiring medical or surgical care, inclusive of changes in medication in the past 2 months indicating that chronic illness/disease is not stable (at the discretion of the investigator). This includes any current workup of undiagnosed illness that could lead to a new condition.

• Chronic disease inclusive of: a) hypertension uncontrolled for age according to the Eighth Joint National Committee (JNC 8) guidelines; b) congestive heart failure by New York Heart Association (NYHA) functional classification of greater or equal to II; c) chronic obstructive pulmonary disease by Global Initiative for Obstructive Lung Disease (GOLD) classification of greater or equal to 2; d) recent (within 6 months prior to first study vaccination) exacerbation of coronary artery disease as manifested by cardiac intervention, addition of new cardiac medications for control of symptoms, or unstable angina; e) asthma (diagnosed by spirometry showing reversibility of disease and must meet at least the Step 1 classification with current prescription/use of medications to control symptoms); f) diabetes requiring use of medicine (insulin or oral) or not controlled with diet.

• Participation in research involving an investigational product (drug/biologic/device) within 45 days prior to first study vaccination.

• History of a confirmed diagnosis of SARS or COVID-19 disease (confirmed by a specific test for each disease) or known exposure to a SARS-CoV-2 positive confirmed close contact (eg, family member, housemate, daycare provider, aged parent requiring care), at the discretion of the investigator.

• Currently working in an occupation with a high risk of exposure to SARS-CoV-2 (eg, healthcare worker, emergency response personnel).

• Currently taking any product (investigational or off-label) for prevention of COVID-19 disease.

• Positive rapid test for SARS-CoV-2 (either ELISA IgG or PCR) at screening or prior to first vaccination. Testing may be repeated during the screening period if exposure to SARS-CoV-2 is suspected, at the discretion of the investigator.

• Received influenza vaccination within 14 days prior to first study vaccination, or any other vaccine within 4 weeks prior to first study vaccination.

• Any autoimmune or immunodeficiency disease/condition (iatrogenic or congenital).

• Chronic administration (defined as more than 14 continuous days) of immunosuppressant, systemic glucocorticosteroids, or other immune-modifying drugs within 90 days prior to first study vaccination; or anticipation of the need for immunosuppressive treatment within 6 months after last vaccination.

• Received immunoglobulin, blood-derived products, or other immunosuppressant drugs within 90 days prior to first study vaccination.

• Any acute illness concurrent or within 14 days prior to first study vaccination (medical history and/or physical examination) or documented temperature of >38°C during this period. This includes respiratory or constitutional symptoms consistent with SARS-CoV-2 (COVID-19) exposure (ie, cough, sore throat, difficulty breathing).

• Known disturbance of coagulation (iatrogenic or congenital).

• Evidence of Hepatitis B or C or HIV by laboratory testing.

• A positive test result for drugs of abuse (except a positive test result associated with prescription medication that has been reviewed and approved by the investigator) or alcohol at screening.

• Any neurological disease or history of significant neurological disorder (eg, meningitis, seizures, multiple sclerosis, vasculitis, migraines, Guillain-Barré syndrome [genetic/congenital or acquired]).

• Active cancer (malignancy) within 5 years prior to first study vaccination (with the exception of adequately treated non-melanomatous skin carcinoma, at the discretion of the investigator)

• Vital sign (blood pressure, pulse, temperature) abnormalities of toxicity grade >1.

• Clinical laboratory abnormalities of toxicity grade >1 for selected serum chemistry and hematology parameters

• Any known allergies to products contained in the investigational product or latex allergy.

• Women who are pregnant, breastfeeding or who plan to become pregnant during the study.

• History of alcohol abuse or drug addiction within 1 year prior to the first study vaccination.

• Any condition that, in the opinion of the investigator, would pose a health risk to the participant if enrolled or could interfere with evaluation of the study vaccine or interpretation of study results (including neurologic or psychiatric conditions deemed likely to impair the quality of safety reporting).

• Study team member or first-degree relative of any study team member (inclusive of sponsor, PPD, and site personnel involved in the study).

Inclusion Criteria (Part 2):

• Healthy adult males or females between 18 and 84 years of age, inclusive, at screening who are of legal adult age in their local jurisdiction. Healthy status will be determined by the investigator based on medical history, clinical laboratory results, vital sign measurements, and physical examination at screening.

• The participant has a body mass index 17 to 35 kg/m2, inclusive, at screening.

• Willing and able to give informed consent prior to study enrollment and comply with study procedures.

• Female participants of childbearing potential (defined as any female who has experienced menarche and who is NOT surgically sterile [ie, hysterectomy, bilateral tubal ligation, or bilateral oophorectomy] or postmenopausal [defined as amenorrhea at least 12 consecutive months or documented plasma FSH level =40 mIU/mL]) must agree to be heterosexually inactive from at least 21 days prior to enrollment and through 6 months after the last vaccination OR agree to consistently use any of the following methods of contraception from at least 21 days prior to enrollment and through 6 months after the last vaccination.

Exclusion Criteria (Part 2):

• Participants who are having any current workup of undiagnosed illness within the last 8 weeks, which is either participant-reported or has been clinician-assessed, that could lead to a new condition diagnosis.

• Participation in research involving an investigational product (drug/biologic/device) within 45 days prior to first study vaccination.

• History of a confirmed diagnosis of SARS or history of a confirmed diagnosis of COVID-19 disease resulting in medical intervention.

• Received influenza vaccination within 14 days prior to first study vaccination, or any other vaccine within 4 weeks prior to first study vaccination.

• Have clinically significant chronic cardiovascular, endocrine, gastrointestinal/ hepatic, renal, neurological, respiratory, or other medical disorders not excluded by other exclusion criteria, that are assessed by the Investigator as being clinically unstable within the prior 4 weeks evidenced by: a) hospitalization for the condition, including day surgical interventions, b) new significant organ function deterioration, c) needing addition of new treatments or major dose adjustments of current treatments.

• Diabetes mellitus requiring insulin therapy (either type 1 or type 2 diabetes mellitus).

• Chronic obstructive pulmonary disease with a history of an acute exacerbation of any severity in the prior year.

• Any history of congestive heart failure.

• Any history of chronic kidney disease (the presence of impaired or reduced kidney function lasting at least 3 months). Clinical validation of potential cases of chronic kidney disease should be conducted.

• Evidence of unstable coronary artery disease as manifested by cardiac intervention, addition of new cardiac medications for control of symptoms, or unstable angina in the past 3 months.

• History of chronic neurological disorders that have required prior specialist physician review for diagnosis and management (such as multiple sclerosis, dementia, transient ischemic attacks, Parkinson's disease, degenerative neurological conditions, neuropathy, and epilepsy) or a history of stroke or previous neurological disorder within 12 months with residual symptoms. Participants with a history of migraine or chronic headaches or nerve root compression that have been stable on treatment for the last 4 weeks are not excluded.

• Any autoimmune or immunodeficiency disease/condition (iatrogenic or congenital).

• Chronic administration (defined as more than 14 continuous days) of immunosuppressants, systemic glucocorticosteroids reaching an immunosuppressive dose, or other immune-modifying drugs within 90 days prior to first study vaccination.

• Received immunoglobulin, blood-derived products, or other immunosuppressant drugs within 90 days prior to first study vaccination.

• Known disturbance of coagulation (iatrogenic or congenital).

• Active cancer (malignancy) within 5 years prior to first study vaccination (with the exception of adequately treated non-melanomatous skin carcinoma, at the discretion of the investigator).

• Any known allergies to products contained in the investigational product or latex allergy.

• Women who are breastfeeding or who plan to become pregnant during the study.

• History of alcohol abuse or drug addiction within one year prior to the first study vaccination.

• Any condition that, in the opinion of the investigator, would pose a health risk to the subject if enrolled or could interfere with evaluation of the study vaccine or interpretation of study results (including neurologic or psychiatric conditions deemed likely to impair the quality of safety reporting).

• Study team member or first-degree relative of any study team member (inclusive of sponsor, PPD, and site personnel involved in the study).

Related Conditions & MeSH terms

• COVID-19

Intervention

Biological:
• SARS-CoV-2 rS - Phase 1
Alternating intramuscular (deltoid) injections of SARS-CoV-2 rS (0.6 mL) on Days 0 and 21.
• SARS-CoV-2 rS/Matrix-M Adjuvant - Phase 1
Alternating intramuscular (deltoid) injections of SARS-CoV-2 rS mixed with Matrix-M adjuvant (0.6 mL) on Days 0 and 21.

Other:
• Normal saline solution (NSS), Placebo - Phase 1
Alternating intramuscular (deltoid) injections of placebo (0.6 mL) on Days 0 and 21.
• Normal saline solution (NSS), Placebo - Phase 2
Intramuscular (deltoid) injections of placebo (0.5 mL).

Biological:
• SARS-CoV-2 rS/Matrix-M Adjuvant, Day 0 - Phase 1
Intramuscular (deltoid) injection of SARS-CoV-2 rS mixed with Matrix-M adjuvant (0.6 mL) on Day 0.

Other:
• Normal saline solution (NSS), Placebo, Day 21 - Phase 1
Intramuscular injection of placebo (0.6 mL) in alternate deltoid on Day 21.

Biological:
• SARS-CoV-2 rS/Matrix-M Adjuvant - Phase 2
Intramuscular (deltoid) injections of SARS-CoV-2 rS co-formulated with Matrix-M adjuvant (0.5 mL).

Locations

Country	Name	City	State
Australia	Paratus Clinical Research - Western Sydney - Phase 2	Blacktown	New South Wales
Australia	Paratus Clinical Research - Canberra - Phase 2	Bruce	Australian Capital Territory
Australia	Barwon Health - Phase 2	Geelong	Victoria
Australia	Q Pharm Pty Limited - Phase 1	Herston	Queensland
Australia	Paratus Clinical Research - Central Coast - Phase 2	Kanwal	New South Wales
Australia	Australian Clinical Research Network - Phase 2	Maroubra	New South Wales
Australia	Center for Clinical Studies - Phase 1 and Phase 2	Melbourne	Victoria
Australia	University of the Sunshine Coast, Health Hub Morayfield - Phase 2	Morayfield	Queensland
Australia	Scientia Clinical Research Limited - Phase 2	Randwick	New South Wales
Australia	University of the Sunshine Coast - Phase 2	Sippy Downs	Queensland
United States	Synexus Clinical Research US, Inc. - Cincinnati - Phase 2	Cincinnati	Ohio
United States	Rapid Medical Research Inc - ERN-PPDS - Phase 2	Cleveland	Ohio
United States	Central Kentucky Research Associates Inc - Phase 2	Lexington	Kentucky
United States	Advanced Clinical Research - Meridian - ERN-PPDS - Phase 2	Meridian	Idaho
United States	Alliance for Multispecialty Research, LLC - Phase 2	Newton	Kansas
United States	Meridian Clinical Research-(Rockville Maryland) - Platinum - PPDS - Phase 2	Rockville	Maryland
United States	Meridian Clinical Research-(Savannah Georgia) - Platinum - PPDS - Phase 2	Savannah	Georgia
United States	Alliance for Multispecialty Research, LLC - Phase 2	Wichita	Kansas

Sponsors (2)

Lead Sponsor	Collaborator
Novavax	Coalition for Epidemic Preparedness Innovations

Countries where clinical trial is conducted

United States,  Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Participants with Solicited Adverse Events (AEs) - Phase 1	Percentage of participants with solicited AEs (local, systemic) for 7 days following each primary vaccination (Days 0, 21) by severity score, duration, and peak intensity.	28 days
Primary	Safety Laboratory Values (Serum Chemistry, Hematology) - Phase 1	Safety laboratory values (serum chemistry, hematology) by FDA toxicity scoring (absolute and change from baseline where identified) at 7 days after each vaccination.	28 days
Primary	Serum Immunoglobulin G (IgG) Antibody Levels Expressed as Geometric Mean Titers (GMTs) - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by enzyme-linked immunosorbent assay (ELISA) expressed as GMTs through Day 21.	21 days
Primary	Serum Immunoglobulin G (IgG) Antibody Levels Expressed as Geometric Mean Titers (GMTs) - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by enzyme-linked immunosorbent assay (ELISA) expressed as GMTs through Day 35.	35 days
Primary	Serum IgG Antibody Levels Expressed as Geometric Mean Fold Rises (GMFRs) - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMFRs through Day 35.	35 days
Primary	Serum IgG Antibody Levels Expressed as Seroconversion Rates (SCRs) - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as SCRs through Day 35. SCR is the proportion of participants with =4-fold rises in ELISA units.	35 days
Primary	Serum IgG Antibody Levels Expressed as GMEUs - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMTs for the two-dose regimens by dose at Day 35 regardless of baseline immune status and stratified by baseline immune status.	Day 35
Primary	Serum IgG Antibody Levels Expressed as GMFRs - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMFRs for the two-dose regimens by dose at Day 35 regardless of baseline immune status and stratified by baseline immune status.	Day 35
Primary	Serum IgG Antibody Levels Expressed as SCRs - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as SCRs (=4-fold rises) for the two-dose regimens by dose at Day 35 regardless of baseline immune status and stratified by baseline immune status.	Day 35
Primary	Participants with Solicited Adverse Events (AEs) - Phase 2	Percentage of participants with solicited AEs (local, systemic) for 7 days following each primary vaccination (Days 0 and 21) by severity score, duration, and peak intensity.	28 days
Primary	Participants with Unsolicited AEs - Phase 2	Percentage of participants with unsolicited AEs (eg, treatment-emergent, serious, suspected unexpected serious, those of special interest, all medically attended adverse events [MAAEs]) through the 35 days by Medical Dictionary of Regulatory Activities (MedDRA) classification, severity score, and relatedness.	35 days
Secondary	Participants with Unsolicited AEs - Phase 1	Percentage of participants with unsolicited AEs (eg, treatment-emergent, serious, suspected unexpected serious, those of special interest, all MAAEs) through the first 49 days by MedDRA classification, severity score, and relatedness.	49 days
Secondary	Participants with Abnormal Vital Signs - Phase 1	Percentage of participants with vital sign abnormalities on the day of vaccination by severity scoring immediately following vaccination.	21 days
Secondary	Changes from Baseline in Body Temperature - Phase 1	Mean changes from baseline in body temperature by treatment group and visit.	189 days
Secondary	Changes from Baseline in Blood Pressure - Phase 1	Mean changes from baseline in blood pressure by treatment group and visit.	189 days
Secondary	Changes from Baseline in Pulse Rate - Phase 1	Mean changes from baseline in pulse rate by treatment group and visit.	189 days
Secondary	Participants with MAAEs - Phase 1	Percentage of participants with MAAEs, defined as AEs that lead to an unscheduled visit to a healthcare practitioner, through Day 105 by MedDRA classification, severity score, and relatedness.	105 days
Secondary	Participants with Related MAAEs; Serious Adverse Events (SAEs); and Adverse Events of Special Interest (AESI) - Phase 1	Percentage of participants with MAAEs assessed as related to study vaccine, SAEs, and AESIs until the end of the study (EOS) by MedDRA classification and severity score. All SAEs and AESI, defined as potential immune-mediated medical conditions or AEs relevant to COVID-19, by MedDRA classification, severity score, and relatedness.	386 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMTs at Multiple Time Points - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMTs at multiple time points through Day 189.	189 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMFRs at Multiple Time Points - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMFRs at multiple time points through Day 189.	189 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as SCRs at Multiple Time Points - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as SCRs (proportion of participants with =2-fold and =4-fold rises in antibody levels) at multiple time points through Day 189.	189 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed by Seroresponse Rates (SRRs) at Multiple Time Points - Phase 1	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as SRRs (proportion of participants with rises in ELISA units exceeding the 95th percentile of placebo participants) at multiple time points through Day 189.	189 days
Secondary	Angiotensin-Converting Enzyme 2 (ACE2) Receptor Binding Inhibition Assay Expressed as GMTs - Phase 1	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as GMTs at multiple time points through Day 189.	189 days
Secondary	ACE2 Receptor Binding Inhibition Assay Expressed as GMFRs - Phase 1	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as GMFRs at multiple time points through Day 189.	189 days
Secondary	ACE2 Receptor Binding Inhibition Assay Expressed as SCRs - Phase 1	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as SCRs at multiple time points through Day 189.	189 days
Secondary	ACE2 Receptor Binding Inhibition Assay Expressed as SRRs - Phase 1	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as SRRs at multiple time points through Day 189.	189 days
Secondary	Neutralizing Antibody Activity Expressed as GMTs - Phase 1	Neutralizing antibody activity as detected by microneutralization assay (MN) expressed as GMTs at multiple time points through Day 49.	49 days
Secondary	Neutralizing Antibody Activity Expressed as GMFRs - Phase 1	Neutralizing antibody activity as detected by MN expressed as GMFRs at multiple time points through Day 49.	49 days
Secondary	Neutralizing Antibody Activity Expressed as SCRs - Phase 1	Neutralizing antibody activity as detected by MN expressed as SCRs at multiple time points through Day 49.	49 days
Secondary	Neutralizing Antibody Activity Expressed as SRRs - Phase 1	Neutralizing antibody activity as detected by MN expressed as SRRs at multiple time points through Day 49.	49 days
Secondary	Assessment of Cell-Mediated (T helper 1 [Th1]/T helper 2 [Th2]) Pathways - Phase 1	Cell-mediated (Th1/Th2) pathways as measured by whole blood (flow cytometry) and/or in vitro peripheral blood mononuclear cell (PBMC) stimulation (eg, enzyme-linked immunospot [ELISpot], cytokine staining) with SARS-CoV-2 rS protein(s) through Day 28.	28 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMTs - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMTs for the single-dose regimens compared to the two-dose regimens and to placebo through Day 35 regardless of baseline immune status and stratified by baseline immune status.	35 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMFRs - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMFRs for the single-dose regimens compared to the two-dose regimens and to placebo through Day 35 regardless of baseline immune status and stratified by baseline immune status.	35 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as SCRs (= 4-fold change) - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as SCRs (= 4-fold change) for the single-dose regimens compared to the two-dose regimens and to placebo through Day 35 regardless of baseline immune status and stratified by baseline immune status.	35 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMEUs at Multiple Time Points - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMTs at multiple time points through Day 357 for the single-dose regimens compared to the two-dose regimens and to placebo, stratified by baseline immune response.	357 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMFRs at Multiple Time Points - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMFRs at multiple time points through Day 357 for the single-dose regimens compared to the two-dose regimens and to placebo, stratified by baseline immune response.	357 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as SCRs (= 4-fold change) at Multiple Time Points - Phase 2	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as SCRs (= 4-fold change) at multiple time points through Day 357 for the single-dose regimens compared to the two-dose regimens and to placebo, stratified by baseline immune response.	357 days
Secondary	ACE2 Receptor Binding Inhibition Assay Expressed as GMTs - Phase 2	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as GMTs at multiple time points through Day 357 for the single-dose regimens compared to the two-dose regimens and to placebo.	357 days
Secondary	ACE2 Receptor Binding Inhibition Assay Expressed as GMFRs - Phase 2	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as GMFRs at multiple time points through Day 357 for the single-dose regimens compared to the two-dose regimens and to placebo.	357 days
Secondary	ACE2 Receptor Binding Inhibition Assay Expressed as SCRs - Phase 2	Epitope-specific immune responses to the SARS-CoV-2 rS protein receptor binding as detected by ACE2 receptor binding inhibition assay expressed as SCRs (= 4-fold change) at multiple time points through Day 357 for the single-dose regimens compared to the two-dose regimens and to placebo.	357 days
Secondary	Neutralizing Antibody Activity Expressed as GMTs - Phase 2	Neutralizing antibody activity as detected by MN expressed as GMTs at Days 35, 217, and 357 relative to baseline in a subset of subjects by absolute titers and change from baseline.	357 days
Secondary	Neutralizing Antibody Activity Expressed as GMFRs - Phase 2	Neutralizing antibody activity as detected by MN expressed as GMFRs at Days 35, 217 and 357 relative to baseline in a subset of subjects by absolute titers and change from baseline.	357 days
Secondary	Neutralizing Antibody Activity Expressed as SCRs (= 4-fold change) - Phase 2	Neutralizing antibody activity as detected by MN expressed as SCRs (= 4-fold change) at Days 35, 217, and 357 relative to baseline in a subset of subjects by absolute titers and change from baseline.	357 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMTs - Phase 2 Boost	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMTs at Days 189, 217, and 357 for all treatment groups and additionally at Day 371 and Day 546 for treatment groups B and C for boosting assessment with either placebo or active boost.	546 days
Secondary	Assessment of Serum IgG Antibody Levels Expressed as GMFRs - Phase 2 Boost	Serum IgG antibody levels specific for the SARS-CoV-2 rS protein antigen(s) as detected by ELISA expressed as GMFRs at Days 189, 217, and 357 for all treatment groups and additionally at Day 371 and Day 546 for treatment groups B and C for boosting assessment with either placebo or active boost.	546 days
Secondary	Participants with MAAEs - Phase 2	All MAAEs, defined as AEs that lead to an unscheduled visit to a healthcare practitioner, through Day 217 by MedDRA classification, severity score, and relatedness.	217 days
Secondary	Participants with Related MAAEs; SAEs; and AESIs - Phase 2	Percentage of participants with MAAEs assessed as related to study vaccine, SAEs, and AESIs until the end of the study (EOS) by MedDRA classification and severity score. All SAEs and AESI, defined as potential immune-mediated medical conditions or AEs relevant to COVID-19, by MedDRA classification, severity score, and relatedness.	357 days
Secondary	Participants with Abnormal Vital Signs - Phase 2	Percentage of participants with vital sign abnormalities on the day of vaccination by severity scoring immediately following vaccination. Descriptive statistics (mean, standard deviation, change from baseline) by treatment group, by visit.	21 days
Secondary	Changes from Baseline in Body Temperature - Phase 2	Mean changes from baseline in body temperature by treatment group and visit.	189 days
Secondary	Changes from Baseline in Blood Pressure - Phase 2	Mean changes from baseline in blood pressure by treatment group and visit.	189 days
Secondary	Changes from Baseline in Pulse Rate - Phase 2	Mean changes from baseline in pulse rate by treatment group and visit.	189 days
Secondary	Participants with SARS-CoV-2 Positivity - Phase 2	Percentage of participants with SARS-CoV-2 positivity as diagnosed by qualitative polymerase chain reaction (PCR) following COVID-19 symptoms assessment from Day 28 through 6 months with severity classification, overall and by age strata (18-59, 60-84 years).	161 days
Secondary	Assessment of SARS-CoV-2 by Qualitative PCR - Phase 2	Assessment of SARS-CoV-2 by qualitative PCR based on routine screening by self- collection (nasal mid-turbinate or saliva) from Day 28 through 6 months without symptomatology to further describe epidemiologic evolution of the pandemic and potential effect of vaccination.	161 days
Secondary	Assessment of Cell-Mediated (Th1/Th2) Pathways - Phase 2	Assessment of cell-mediated (Th1/Th2) pathways as measured by whole blood (flow cytometry) and/or in vitro PBMC stimulation (eg, ELISpot, cytokine staining) with SARS-CoV-2 rS protein(s) through Day 28.	28 days