A Study to Evaluate VXA-CoV2-3.1 COVID-19 Vaccine Against Currently Approved/Authorized mRNA COVID-19 Injectable Booster Vaccine in Adults Previously Immunized Against COVID-19 Infection

Launched by VAXART · Nov 1, 2024

Keywords

ClinConnect Summary

This clinical trial is investigating a new oral COVID-19 vaccine called VXA-CoV2-3.1. The goal is to see how well this vaccine works compared to currently recommended mRNA booster vaccines in adults who have already received their primary COVID-19 vaccinations. If you're an adult aged 18 or older and have had your last COVID-19 vaccine at least six months ago, you may be eligible to participate. Additionally, you should have received at least two doses of an mRNA vaccine before enrolling.

Participants in this study can expect to receive either the new oral vaccine or the standard injectable booster. You'll need to be available for several visits and will undergo some health checks to ensure you're stable and can safely take part in the trial. It's important to note that certain medical conditions or recent vaccinations may affect eligibility, so a thorough screening will be conducted. This trial aims to provide more options for COVID-19 vaccination and help protect against the virus in the future.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Adults 18 years of age and above, at time of screening.
• • 2. Completed primary approved/authorized COVID-19 vaccination series with ≥ 2 mRNA vaccine doses.
• • 3. Last COVID-19 vaccine received ≥6 months prior to study vaccination.
• • 4. Male and female participants of childbearing potential must agree to consistently use a highly effective method of contraception from at least 30 days prior to enrollment and through 3 months after the last study vaccination.
• • 5. Is medically stable, as determined by the site investigator (based on review of health status, vital signs, medical history, and physical examination) with screening lab values within normal limits or abnormalities assessed as not clinically significant.
• • 6. Agree to not participate in any other SARS-CoV-2 infection prevention trial (vaccine, drug, biologic, PrEP) during participation in the study.
• • 7. Willing and able to provide informed consent prior to initiation of study procedures.
• • 8. Available for all study visits, willing to participate in all study procedures, and not planning to relocate from the area for the duration of the study.
• • 9. Negative rapid molecular Covid test at the screening visit and on Day 1 prior to vaccine dosing.
• Exclusion Criteria:
• 1. Participant has an acute illness as defined by any of the following (note: assessment may be repeated once during screening period):
• • a. As determined by the site investigator, within 72 hours prior to vaccination.
• • i. An acute illness that is nearly resolved, with only minor residual symptoms remaining, is allowable if, in the opinion of the site investigator, the residual symptoms will not interfere with the ability of study staff to assess safety parameters as required by the protocol. b. Presence of a fever ≥ 38.0°C (100.4°F) measured orally at baseline, on Day 1 prior to vaccination. c. Receipt of antipyretic/analgesic medications within 24 hours prior to vaccine administration.
• • 2. Participant has had a positive COVID test within 90 days prior to screening.
• • 3. Current or planned participation in any other interventional clinical trial.
• • 4. Participation in research involving any investigational product within 45 days prior to study vaccination.
• • 5. Receipt of any approved or authorized products intended to prevent SARS-CoV2 infection within 6 months prior to study vaccination.
• • 6. Receipt or donation of blood products or immunoglobulins within 60 days prior to enrollment or planned administration during the study.
• • 7. Received influenza vaccination within 14 days prior to study vaccination, or any other vaccine within 30 days prior to study vaccination.
• • 8. Any autoimmune or immunodeficiency disease/condition (including and not limited to untreated or advanced HIV infection with CD4 counts \<200 cells/mm\^3, history of AIDS defining illness without immune reconstitution, or clinical manifestations of symptomatic HIV, severe combined immunodeficiency (SCID), hypogammaglobulinemia, asplenia or functional asplenia).
• • 9. Unstable medical or psychiatric illness (acute or chronic illness) requiring significant medical monitoring and intervention during the 90 days prior to enrollment. Note: diabetes mellitus (Types 1 \& 2) are not excluded if assessed by the principal investigator (PI) as well-controlled.
• 10. Administration of immunosuppressants, systemic glucocorticoids, or other immune-modifying drugs within the following timeframes:
• • 1. B-cell therapies within the 6 months prior to first study vaccination
• • 2. Prednisone, ≥20 mg for more than 2 weeks, within the 30 days prior to study vaccination
• • 3. Other medications in this category, including but not limited to high-dose inhaled corticosteroids (\>800 mcg/day of beclomethasone dipropionate or equivalent); antimetabolites; transplant immunosuppressive agents; alkylating agents; cell-depleting agents; or cancer chemotherapeutics, within the 90 days prior to study vaccination.
• • 4. Any medication for any period of time that, in the opinion of the site investigator, could impede immune response to vaccination.
• • 5. Use of any dose montelukast OR inhaled, intranasal, intra-articular, or systemic corticosteroids within 2 weeks prior to study vaccination.
• • 6. Planned use of any of these medications during the study.
• • 11. Known contraindication to IM injection or blood draws (e.g. bleeding diathesis, acquired coagulopathy, significant bleeding or bruising) or to oral route of administration (unable to swallow tablets).
• • 12. Any known allergies to components contained in the investigational product (including fish gelatin) or comparator or latex allergy (including polyethylene glycol \[PEG\] allergies) and/or history of serious reactions to vaccination such as anaphylaxis, respiratory problems, hives, or abdominal pain.
• • 13. Women who are pregnant (pregnancy tests will be performed at screening and prior to dosing), breastfeeding, or who plan to become pregnant during the study.
• 14. History of irritable bowel disease or other inflammatory digestive or gastrointestinal condition that could affect the distribution/safety evaluation of an orally administered vaccine targeting the mucosa of the small intestine. Such conditions may include but are not limited to:
• • a. Any history of: i. GI malignancy ii. malabsorption iii. pancreatobiliary disorders iv. inflammatory bowel disease v. irritable bowel disease vi. hiatal hernia vii. surgical resection b. History of diagnosis or treatment in past 5 years of: i. esophageal or gastric motility disorder ii. gastroesophageal reflux disorder iii. peptic ulcer iv. cholecystectomy.
• • 15. Use of antibiotics, proton pump inhibitors, H2 blockers, or antacids within 7 days prior to study drug administration or planned use during the study.
• • 16. Use of drugs known to affect gastrointestinal motility including glucagon-like peptide 1 (GLP-1) receptor agonists including tirzepatide (Mounjaro) and semaglutide (Wegovy, Ozempic) within 30 days prior to drug administration.
• • 17. Daily use of nonsteroidal anti-inflammatory drugs within 7 days prior to study drug administration or planned use during the study.
• • 18. Personal or familial history of hypercoagulable states to include personal past history of deep vein thrombosis (DVT).
• • 19. Personal history of myocarditis or pericarditis.
• • 20. Positive Hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV) antibody at the screening visit.
• • 21. History of drug, alcohol, or chemical abuse within 1 year of screening.
• • 22. Positive urine drug screen for drugs of abuse at screening (except for previous marijuana use); concurrent or planned use of marijuana during the active study period are excluded. Positive urine drug screen (UDS) at screening due to prescribed stimulants will be reviewed on a case by case basis.
• • 23. Cancer, or treatment for cancer, within the past 3 years (excluding fully treated and resolved basal cell carcinoma or squamous cell carcinoma).
• • 24. History of any form of angioedema.
• • 25. History of GI bleeding including hematochezia (blood in stool) or melena (black stool) of unknown etiology or that has not been evaluated.
• 26. Any history or conditions that may lead to a higher risk of clotting events and/or thrombocytopenia, including:
• • 1. Familial coagulopathy or personal history of bleeding disorder or thrombosis
• • 2. History of heparin-related thrombotic events, and/or receiving heparin treatments
• • 3. History of autoimmune or inflammatory disease
• 4. Presence of any of the following conditions known to increase the risk of thrombosis within 6 months prior to screening:
• • i. Recent surgery other than fully healed cesarean delivery or excision/ biopsy of cutaneous lesions ii. Immobility (confined to bed or wheelchair for 3 or more successive days) iii. Head trauma with loss of consciousness or documented brain injury iv. Receipt of anticoagulants for prophylaxis of thrombosis v. Recent clinically significant infection including hospitalization for COVID-19 related illness.
• • 27. 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 investigational product or interpretation of study results.
• • 28. Study team member or first-degree relative of any study team member (inclusive of sponsor and site personnel involved in the study).