A Study to Evaluate the Immunogenicity and Safety of mRNA-1283 COVID-19 Vaccine Boosters
The main goal of this study is to assess the safety, reactogenicity, and immunogenicity of the study vaccines.
- Eligible Ages
- Over 18 Years
- Eligible Genders
- Accepts Healthy Volunteers
- Female participants of nonchildbearing potential may be enrolled in the study. Nonchildbearing potential is defined as bilateral tubal ligation >1 year prior to screening, bilateral oophorectomy, hysterectomy, or menopause. - Female participants of childbearing potential may be enrolled in the study if the participant has a negative pregnancy test on the day of vaccination (Day 1), practiced adequate contraception or has abstained from all activities that could result in pregnancy for at least 28 days prior to Day 1, agreed to continue adequate contraception through 3 months following the last vaccine administration, and not currently breastfeeding. - Participant must have received their second dose of mRNA-1273 vaccine at least 6 months prior to screening and enrollment.
- Had significant exposure to someone with SARS-CoV-2 infection or COVID-19 in the past 14 days, defined by the US Centers for Disease Control and Prevention (CDC) as a close contact of someone who has COVID-19. - Is acutely ill or febrile (temperature ≥38.0 degree Celsius [°C]/100.4 degree Fahrenheit [°F]) less than 72 hours prior to or at the screening visit or Day 1. - Has a medical, psychiatric, or occupational condition that may pose additional risk as a result of participation, or that could interfere with safety assessments or interpretation of results according to the investigator's judgment. - Has received systemic immunosuppressants or immune-modifying drugs for >14 days in total within 6 months prior to screening (for corticosteroids ≥10 milligrams [mg]/day of prednisone equivalent) or is anticipating the need for immunosuppressive treatment at any time during participation in the study. - Has received or plans to receive any licensed vaccine ≤28 days prior to the injection (Day 1) or plans to receive a licensed vaccine within 28 days before or after the study injection, with the exception of influenza vaccines, which may be given 14 days before or after receipt of a study vaccine. - Has received systemic immunoglobulins or blood products within 3 months prior to the screening visit, or plans to receive these during the study. - Has donated ≥ 450 milliliters (mL) of blood products within 28 days prior to the screening visit or plans to donate blood products during the study. - Plans to participate in an interventional clinical trial of an investigational vaccine or drug while participating in this study. Note: Other inclusion and exclusion criteria may apply.
- Phase 2
- Study Type
- Intervention Model
- Parallel Assignment
- Primary Purpose
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
mRNA-1283 Dose Level 1
|Participants will receive single intramuscular (IM) injection of mRNA-1283 at Dose Level 1 on Day 1.||
mRNA-1283 Dose Level 2
|Participants will receive single IM injection of mRNA-1283 at Dose Level 2 on Day 1.||
mRNA-1283 Dose Level 3
|Participants will receive single IM injection of mRNA-1283 at Dose Level 3 on Day 1.||
mRNA-1283.211 Dose Level 1
|Participants will receive single IM injection of mRNA-1283.211 at Dose Level 1 on Day 1.||
mRNA-1283.211 Dose Level 2
|Participants will receive single IM injection of mRNA-1283.211 at Dose Level 2 on Day 1.||
|Participants will receive single IM injection of mRNA-1273 on Day 1.||
Hollywood, Florida 33024-2709
Chamblee, Georgia 30341
Metairie, Louisiana 70006
Worcester, Massachusetts 01655-0002
Minneapolis, Minnesota 55402-2700
Lincoln, Nebraska 68510
Albuquerque, New Mexico 87102-3876
Cincinnati, Ohio 45212
Cincinnati, Ohio 45246-2316
Columbus, Ohio 43213-6517
Frisco, Texas 75033-4135
- NCT ID
- ModernaTX, Inc.
Study ContactModerna Clinical Trials Support Center
This study will assess whether a single dose of mRNA-1283 at three different dose levels or mRNA-1283.211 at two different dose levels will boost antibody responses to the Wuhan-Hu-1 (ancestral strain of SARS-CoV-2) virus, and to the B.1.351 variant, and potentially other SARS-CoV-2 variants, and it will also be used to select a dose for subsequent clinical evaluation. The study will include an active comparator group of participants who will receive mRNA-1273. Participants who received the primary series of mRNA-1273 with appropriate documentation at least 6 months prior will be randomized 1:1:1:1:1:1 to receive a single boost of mRNA-1283 at one of three dose levels, a single boost of mRNA-1283.211 at one of two dose levels, or a single dose of the active comparator, mRNA-1273.