Efficacy and Safety of NVX-CoV2705

Running, not enrolling · Phase 4 · Has a placebo group

Conditions studied: COVID-19, Sars-CoV-2 Infection

In brief

This is a Phase 4, post-market US study, evaluating the efficacy and safety of a single dose of the NVX-CoV2705 Omicron JN.1 COVID-19 vaccine. Approximately 6,500 healthy adults aged 50 to under 65 will be randomized to receive either the vaccine or a placebo, with follow-up for 180 days.

Key facts

Study ID

NCT07086222

Run by

Novavax

People needed

6500

Starts

2025-11-20

Expected to finish

2026-11-18

Last updated by the study team

2026-05-08

Who can join

Age: 50 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• To be included in this study, each individual must satisfy all of the following criteria:
• Adults 50 to < 65 years of age at time of study vaccination (Day 0) who are not considered to be at high risk of severe COVID-19.
• Participants unvaccinated to SARS-CoV-2 or participants previously vaccinated with a COVID-19 vaccine ≥ 90 days prior to study vaccination.
• Participant or legally acceptable representative is 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 inactive from at least 28 days prior to enrollment and through 90 days after vaccination OR agree to consistently use a medically acceptable method of contraception listed below from ≥ 28 days prior to enrollment and through 90 days after vaccination.
• 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.
• Agrees not to 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.

You may not qualify if…

• If an individual meets any of the following criteria, he or she is ineligible for this study:
• Is considered to be at high risk of severe COVID-19 due to underlying medical conditions or risk factors that demonstrated a conclusive increase in risk for at least one severe COVID-19 outcome, as described by the Centers for Disease Control and Prevention (CDC) .
• Unstable acute illness at the time of vaccination.
• Participation at the time of study enrollment or planned participation during the present study period in another clinical study investigating a vaccine, drug, medical device, or medical procedure.
• Current participation in any other COVID-19 prevention clinical trial.
• Known history of COVID-19 infection within 90 days of study vaccination.
• Any known history of allergies to products contained in the investigational product in the participant's lifetime.
• Any known history of anaphylaxis to any prior vaccine in the participant's lifetime.
• Known history of myocarditis or pericarditis in the participant's lifetime.
• Chronic administration (defined as > 14 continuous days) of immunosuppressant, systemic glucocorticoids, 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, inhaled, or intranasal glucocorticoids is permitted. Topical tacrolimus and ocular cyclosporin are permitted.
• Received immunoglobulin or blood-derived products within 90 days prior to study vaccination (Day 0).
• Participants who are pregnant, or who plan to become pregnant within 90 days following study vaccination.
• 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, clinical research organization [CRO], and study site personnel involved in the conduct or planning of the study).

Where it is running

• TrialMed - Birmingham — Birmingham, Alabama, United States
• Hawthorne Health - Gadsden — Gadsden, Alabama, United States
• TrialdMed - Huntsville — Huntsville, Alabama, United States
• AMR Mobile — Mobile, Alabama, United States
• Headlands Research Scottsdale — Scottsdale, Arizona, United States
• Orange Grove Family Practice — Tucson, Arizona, United States
• 310 Clinical Research — Inglewood, California, United States
• Velocity Clinical Research - San Diego — La Mesa, California, United States
• Profound Research LLC at Seaside Medical Group — Oceanside, California, United States
• California Research Foundation — San Diego, California, United States
• Bayview Research Group, LLC — Valley Village, California, United States
• Diablo Clinical Research, Inc. — Walnut Creek, California, United States
• Alliance Clinical - West Hills — West Hills, California, United States
• Lynn Institute of Denver — Aurora, Colorado, United States
• Paradigm Clinical Research Centers, LLC — Wheat Ridge, Colorado, United States
• Clinical Research Consulting, LLC — Milford, Connecticut, United States
• SIMED Health, LLC / SIMED Research — Gainesville, Florida, United States
• Indago Research and Health Center, Inc. — Hialeah, Florida, United States
• Health Awareness, LLC — Jupiter, Florida, United States
• TrialMed - Melbourne — Melbourne, Florida, United States
• Acevedo Clinical Research Associates — Miami, Florida, United States
• Research Institute Of South Florida, Inc. — Miami, Florida, United States
• MOORE Clinical Research — Tampa, Florida, United States
• TrialMed - The Villages — The Villages, Florida, United States
• North Alabama Research Center — Athens, Alabama, United States

Full record on ClinicalTrials.gov

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