A Study to Evaluate the Safety and Immunogenicity of an (Omicron Subvariant) COVID-19 Vaccine Booster Dose in Previously Vaccinated Participants and Unvaccinated Participants.

Completed · Phase 2/Phase 3

Conditions studied: COVID-19

In brief

This is a Phase 2/3 open-label study to evaluate the safety and immunogenicity of a booster dose of the XBB.1.5 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) recombinant (r) spike (S) protein nanoparticle vaccine (SARS-CoV-2 rS) adjuvanted with Matrix-M™ in previously mRNA COVID-19 vaccinated adult participants ≥18 years of age and baseline SARS CoV-2 seropositive COVID-19 vaccine naïve participants ≥18 years of age.

Key facts

Study ID

NCT05975060

Run by

Novavax

People needed

660

Starts

2023-09-07

Expected to finish

2024-05-20

Last updated by the study team

2024-05-30

Who can join

Age: 18 and older, up to 54. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults ≥ 18 years of age at time of study vaccination.
• Part 1: Previously vaccinated with ≥ 3 doses of the Moderna and/or Pfizer /BioNTech prototype monovalent and/or BA.4/5 containing bivalent COVID-19 vaccines with the last dose administered ≥ 90 days prior to study vaccination.
• Part 2: Clinical history of COVID-19-like disease during the previous year.
• 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 ≥ 12 consecutive months]) must agree to be heterosexually in-active 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 ≥ 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 NOTE: Periodic abstinence (eg, calendar, ovulation, sympto-thermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception.
• Is medically stable, as determined by the investigator (based on review of health status, vital signs [to include body temperature], medical history, and physical examination [to include body weight]). Vital signs must be within medically acceptable ranges prior to study vaccination.
• Agrees to not participate in any research involving receipt of investigational products (drug/biologic/device) including other SARS-CoV-2 prevention or treatment trials for the duration of the study.
• NOTE: For participants who become hospitalized with COVID-19, participation in investigational treatment studies is permitted.

You may not qualify if…

• Received COVID-19 vaccines other than Moderna and/or Pfizer-BioNTech in the past, inclusive of clinical trial COVID-19 vaccines.
• Participation in research involving receipt of investigational products (drug/biologic/device) within 90 days prior to study vaccination (Day 0).
• Received influenza vaccination within 14 days prior to study vaccination, or any other vaccine within 30 days prior to 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.
• NOTE: Stable endocrine disorders (eg, thyroiditis, pancreatitis), including stable diabetes mellitus with no history of diabetic ketoacidosis are NOT excluded.
• Chronic administration (defined as > 14 continuous days) of immunosuppressant, systemic glucocorti-coids, or other immune-modifying drugs within 90 days prior to study vaccination (Day 0).
• NOTE: An immunosuppressant dose of glucocorticoid is defined as a systemic dose ≥ 10 mg of prednisone per day or equivalent. The use of topical or intranasal glucocorticoids is permitted. Topical tacrolimus and ocular cyclosporin are permitted. Use of inhaled glucocorticoids is prohibited.
• Received any prohibited medication (see Section 7.4.1), immunoglobulin, blood-derived products, or immunosuppressant drugs within 90 days prior to study vaccination (Day 0).
• Active cancer (malignancy) on chemotherapy within 3 years prior to first study vaccination (with the exception of adequately treated non-melanomatous skin carcinoma or lentigo malign 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 study vaccination 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 (includ-ing 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, clinical research organization [CRO], and study site personnel involved in the conduct or planning of the study).
• Known history of myocarditis or pericarditis.
• Respiratory symptoms in the past 3 days (ie, cough, sore throat, difficulty breathing).
• Temperature of > 38°C within 24 hours of planned study vaccination (site measured or participant meas-ured).
• Blood pressure of ≥ 160/100 mmHg.

Where it is running

• AMR — Mobile, Alabama, United States
• Benchmark Research — Sacramento, California, United States
• Lynn Institute of the Rockies — Colorado Springs, Colorado, United States
• AMR LLC-Miami — Coral Gables, Florida, United States
• AMR — Fort Myers, Florida, United States
• Health Awareness,LLC — Jupiter, Florida, United States
• Tekton Research — Lawrenceville, Georgia, United States
• Alliance for Multispecialty RSCH — Newton, Kansas, United States
• Tekton Research — Wichita, Kansas, United States
• AMR New Orleans — New Orleans, Louisiana, United States
• University of Maryland — Baltimore, Maryland, United States
• AMR — Kansas City, Missouri, United States
• Sundance Clinical Research — St Louis, Missouri, United States
• Velocity Clinical Research — Norfolk, Nebraska, United States
• AMR — Las Vegas, Nevada, United States
• AXCES Research — Albuquerque, New Mexico, United States
• Rochester Clinical Research — Rochester, New York, United States
• Tekton Research — Yukon, Oklahoma, United States
• DM Clinical Research — Philadelphia, Pennsylvania, United States
• AMR — Knoxville, Tennessee, United States
• Benchmark Research — Austin, Texas, United States
• Tekton Research — Austin, Texas, United States
• Tekton Research — Beaumont, Texas, United States
• Pan American clinical Research,LLC — Brownsville, Texas, United States
• Benchmark Research — Fort Worth, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.