Evaluation of the Safety and Immunogenicity of SII Vaccine Constructs Based on the SARS-CoV-2 (COVID-19) Variant in Adults

NCT05029856 | Withdrawn Phase 1

• 1 other identifier: 2019nCoV-102
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 4

Brief Summary

This is a randomized, observer-blinded, Phase 1/2 study with an open-label group to evaluate the safety and immunogenicity of 3 novel SARS-CoV-2 variant vaccine constructs adjuvanted with Matrix-M1 adjuvant. Investigational products will include a monovalent SII SARS-CoV-2 B.1.351 (Beta) variant vaccine (SII B.1.351), a bivalent SII vaccine containing antigen for both the ancestral strain and B.1.351 (Beta) variant of SARS-CoV-2 (SII Bivalent), and a monovalent SII SARS-CoV-2 B.1.617.2 (Delta) variant vaccine (SII B.1.617.2).

Conditions

Covid19

Outcome Measures

Primary Outcomes (7)

• MN50 GMTs to the SARS-CoV-2 B.1.351 (Beta) expressed as GMT

  (MN50) geometric mean titers (GMTs) to the SARS-CoV-2 B.1.351 (Beta) variant at Day 14 (one-dose regimen; Groups C and D) and Day 35 (two-dose regimen; Groups A and B);

  Day 14 and Day 35

• MN50 GMTs to the SARS-CoV-2 B.1.351 (Beta) expressed as SCRs/SRRs

  Seroconversion rates (SCRs) or seroresponse rates (SRRs) (proportion of participants who achieve ≥ 4-fold increase from baseline) in MN50 titer concentrations to the SARS-CoV-2 B.1.351 (Beta) variant following their last vaccination.

  Day 14 and Day 35

• MN50 GMTs to the SARS-CoV-2 B.1.617.2 (Delta)expressed as GMT

  Neutralizing antibody MN50 GMTs to the SARS-CoV-2 B.1.617.2 (Delta) variant at Day 14 (one-dose regimen; Group H) and Day 35 (two-dose regimen; Group G);

  Day 14 and Day 35

• MN50 GMTs to the SARS-CoV-2 B.1.617.2 (Delta)expressed as SCRs/SRRs

  SCRs/SRRs (proportion of participants who achieve ≥ 4-fold increase from baseline) in MN50 titer concentrations to the SARS-CoV-2 Delta variant following their last vaccination.

  Day 14 and Day 35

• Incidence, duration, and severity of solicited local and systemic adverse events (AEs)

  Incidence, duration, and severity of solicited local and systemic adverse events (AEs) for 7 days following each vaccination

  Day 0 to Day 7

• Incidence, duration, severity, and relationship of unsolicited AEs through 28 days

  Incidence, duration, severity, and relationship of unsolicited AEs through 28 days after the last vaccination

  Day 0 to Day 28

• Incidence and relationship of medically attended adverse events (MAAEs), adverse events of special interest (AESIs) (predefined list), and serious adverse events (SAEs)

  Incidence and relationship of medically attended adverse events (MAAEs), adverse events of special interest (AESIs) (predefined list), and serious adverse events (SAEs) throughout the study.

  Day 0 to Day 217

Secondary Outcomes (20)

• MN50 GMTs to the SARS-CoV-2 B.1.351 (Beta) expressed as GMFR in previously vaccinated patients

  Day 0 to Day 189

• MN50 GMTs to the SARS-CoV-2 B.1.351 (Beta) expressed as GMFR in participants seronegative at baseline

  Day 0 to Day 217

• MN50 GMTs to the SARS-CoV-2 B.1.351 (Beta) expressed as SCRs/SRRs in previously vaccinated patients

  Day 0 to Day 189

• MN50 GMTs to the SARS-CoV-2 B.1.351 (Beta) expressed as SCRs/SRRs in participants seronegative at baseline.

  Day 0 to Day 217

• MN50 GMTs to the SARS-CoV-2 B.1.617.2 (Delta) expressed as GMFR in participants seronegative at baseline

  Day 0 to Day 217

Study Arms (8)

Group A- SII B.1.351 Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

2 doses of 3 μg SII B.1.351 Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) . 1 dose each on Days 0 and Day 21.

Biological: SII B.1.351

Group B- SII B.1.351 Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

2 doses of 5 μg SII B.1.351 Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) . 1 dose each on Days 0 and Day 21.

Biological: SII B.1.351

Group C- SII B.1.351 Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

1 dose of 3 μg SII B.1.351 Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) .1 dose on Day 0.

Biological: SII B.1.351

Group D - SII B.1.351 Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

1 dose of 5 μg SII B.1.351 Vaccine + 50 μg Matrix-M1 adjuvant (co-formulated) .1 dose on Day 0.

Biological: SII B.1.351

Group E -SII Bivalent Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

2 doses of 6 μg SII Bivalent Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) . 1 dose each on Days 0 and Day 21.

Biological: SII Bivalent

Group F- SII Bivalent Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

2 doses of 10 μg SII Bivalent Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) . 1 dose each on Days 0 and Day 21.

Biological: SII Bivalent

Group G- SII B.1.617.2 Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

2 doses of 5 μg SII B.1.617.2 Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) . 1 dose each on Days 0 and Day 21.

Biological: SII B.1.617.2

Group H- SII B.1.617.2 Vaccine / Matrix-M1 Adjuvant

EXPERIMENTAL

1 doses of 5 μg SII B.1.617.2 Vaccine+ 50 μg Matrix-M1 adjuvant (co-formulated) . 1 dose on Days 0.

Biological: SII B.1.617.2

Interventions

SII B.1.351 BIOLOGICAL

Intramuscular (deltoid) injections of 3 μg SII B.1.351 and 50 μg Matrix-M1 Adjuvant, 1 or 2 doses:1 on Day 0 and ± 1 on Day 21.

Also known as: (Monovalent B.1.351 [Beta] variant strain vaccine)

Group A- SII B.1.351 Vaccine / Matrix-M1 Adjuvant; Group C- SII B.1.351 Vaccine / Matrix-M1 Adjuvant

SII Bivalent BIOLOGICAL

Intramuscular (deltoid) injections of 6 μg SII Bivalent and 50 μg Matrix-M1 Adjuvant, 2 doses: 1 on Day 0 and 1 on Day 21.

Also known as: (Bivalent ancestral and B.1.351 [Beta] variant strain vaccine)

Group E -SII Bivalent Vaccine / Matrix-M1 Adjuvant

SII B.1.617.2 BIOLOGICAL

Intramuscular (deltoid) injections of 5 μg SII B.1.617.2 and 50 μg Matrix-M1 Adjuvant, 1 or 2 doses:1 on Day 0 and ± 1 on Day 21.

Also known as: (Monovalent B.1.617.2 [Delta] variant strain vaccine)

Group G- SII B.1.617.2 Vaccine / Matrix-M1 Adjuvant; Group H- SII B.1.617.2 Vaccine / Matrix-M1 Adjuvant

Eligibility Criteria

• Age: 18 Years - 64 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Adults 18 to 64 years of age, inclusive, at screening.
• Willing and able to give informed consent prior to study enrollment and to comply with study procedures.
• Female participants of childbearing potential (defined as any participant who has experienced menarche and who is NOT surgically sterile \[ie, hysterectomy, bilateral tubal ligation, or bilateral oophorectomy\] or postmenopausal \[defined as amenorrhea at least 12 consecutive months\]) must agree to be heterosexually inactive from at least 28 days prior to enrollment and through the end of the study OR agree to consistently use a medically acceptable method of contraception listed below from at least 28 days prior to enrollment and through the end of the study.
• Condoms (male or female) with spermicide (if acceptable in country)
• Diaphragm with spermicide
• Cervical cap with spermicide
• Intrauterine device
• Oral or patch contraceptives
• Norplant®, Depo-Provera®, or other in-country regulatory approved contraceptive method that is designed to protect against pregnancy
• Abstinence, as a form of contraception, is acceptable if in line with the participant's lifestyle
• Is medically stable, as determined by the investigator (based on a review of health status, vital signs \[to include body temperature\], medical history, and targeted physical examination \[to include body weight\]). Vital signs must be within medically acceptable ranges prior to the first vaccination.
• Agrees to not participate in any other SARS-CoV-2 prevention or treatment trials for the duration of the study.
• For previously vaccinated Participants (Groups C, D and H):
• Documented receipt of 2 doses of the investigational Novavax vaccine with Matrix-M1 adjuvant (NVX-CoV2373) administered approximately 21 days apart or 2 doses of a TGA-authorized/approved COVID-19 vaccine administered at least 60 days prior to first study vaccination.

You may not qualify if:

• If an individual meets any of the following criteria, he or she is ineligible for this study:
• History of laboratory-confirmed (by PCR or serology to SARS-CoV-2) COVID-19 infection at any time prior to randomization/enrollment.
• Previous receipt of any investigational or authorized/approved vaccine, prophylactic or therapeutic agent for the prevention or treatment of SARS-CoV-2 infection, except for previously vaccinated participants.
• Participation in research involving receipt of investigational products (drug/biologic/device) within 90 days prior to first study vaccination.
• Received influenza vaccination within 14 days prior to first study vaccination, or any other vaccine within 30 days prior to the first study vaccination.
• Any known allergies to products contained in the investigational product.
• Any history of anaphylaxis to any prior vaccine.
• Autoimmune or immunodeficiency disease/condition (iatrogenic or congenital) requiring ongoing immunomodulatory therapy.
• Chronic administration (defined as \> 14 continuous days) of immunosuppressants, systemic glucocorticoids, or other immune-modifying drugs within 90 days prior to first study vaccination.
• Received immunoglobulin, blood-derived products, or immunosuppressant drugs within 90 days prior to first study vaccination.
• Active cancer (malignancy) on therapy within 3 years prior to first study vaccination (with the exception of adequately treated non-melanomatous skin carcinoma or lentigo maligna and uterine cervical carcinoma in situ without evidence of disease, at the discretion of the investigator).
• Participants who are breastfeeding, pregnant, or who plan to become pregnant prior to the end of study.
• Suspected or known history of alcohol abuse or drug addiction within 2 years prior to the first study vaccine dose that, in the opinion of the investigator, might interfere with protocol compliance.
• Any other 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 likely to impair the quality of safety reporting).
• Study team member or immediate family member of any study team member (inclusive of Sponsor, CRO, and study site personnel involved in the conduct or planning of the study).

Sponsors & Collaborators

• Novavax: lead

Study Sites (4)

Australian Clinical Research Network (ACRN)

Maroubra, New South Wales, 2035, Australia

Location

Holdsworth House Medical Practice - Sydney

Sydney, New South Wales, 2010, Australia

Location

University Hospital Geelong-Barwon Health

Geelong, Victoria, 3320, Australia

Location

Emeritus Research

Melbourne, Victoria, 3124, Australia

Location

MeSH Terms

Conditions

COVID-19

Interventions

YY1 Transcription Factor

Condition Hierarchy (Ancestors)

Pneumonia, Viral; Pneumonia; Respiratory Tract Infections; Infections; Virus Diseases; Coronavirus Infections; Coronaviridae Infections; Nidovirales Infections; RNA Virus Infections; Lung Diseases; Respiratory Tract Diseases

Intervention Hierarchy (Ancestors)

Erythroid-Specific DNA-Binding Factors; DNA-Binding Proteins; Proteins; Amino Acids, Peptides, and Proteins; Transcription Factors

Study Officials

• Clinical Development

  Novavax

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 25, 2021
• First Posted: September 1, 2021
• Study Start: February 4, 2022
• Primary Completion: August 1, 2022
• Study Completion: August 1, 2022
• Last Updated: May 31, 2022

Record last verified: 2022-05

Locations

AU (4)