mRNA Covid-19 Vaccine Immune Response Comparisons Using Different Delivery Routes

Launched by PHARMAJET, INC. · Apr 3, 2025

Keywords

ClinConnect Summary

This clinical trial is studying how well the mRNA COVID-19 vaccine works when given in different ways, such as through a special needle-free injection or the traditional needle and syringe. Researchers want to see if these different methods affect the immune response—the body’s defense against the virus that causes COVID-19. The trial will include healthy adults aged 18 to 50 who are in good health and can commit to the study’s requirements, which involve getting vaccinated and attending follow-up visits.

Participants in this trial can expect to receive one of the vaccine delivery methods and will be monitored for their immune response. It's important to note that those with certain health conditions, recent vaccinations, or ongoing medical treatments may not be eligible to participate. This trial is still in the planning stages and is not yet recruiting participants, so more information will be available once it officially begins.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Able to understand and give informed consent
• • 2. Adults aged 18 to 50 years old.
• • 3. Willing and able to comply with all scheduled visits, vaccination, and laboratory tests.
• • 4. Determined by investigator to be in good health based on medical history, targeted physical exam and laboratory testing.
• • 5. Participants with pre-existing stable chronic medical conditions defined as condition not requiring significant change in therapy or hospitalization for worsening disease within 4 weeks from enrollment, can be included at the discretion of the investigator.
• • 6. For women of childbearing potential: willing to engage in effective methods of contraception starting at least 30 days prior to enrollment and for the duration of the study.
• Exclusion Criteria:
• • 1. Receipt of blood products 90 days prior to study entry and for the duration of the study.
• • 2. Volunteers who donated blood 60 days before screening OR will donate blood on or before D30.
• • 3. Receipt of any experimental agents within 30 days or 5 half-lives whichever is longer prior to vaccination and for the duration of the study.
• • 4. Receipt of any licensed vaccine within 60 days prior to study vaccination or planned receipt of any vaccine until 60 days later as well as receipt of COVID-19 vaccine for the duration of the study.
• • 5. Receipt of a COVID-19 vaccine or confirmed COVID-19 in the past year or positive SARS-CoV-2 antigen test on vaccination day.
• • 6. Chronic medical problems including (but not limited to) autoimmune disease, severe gastrointestinal disease, and grade 4 hypertension.
• • 7. Any diseases or conditions that put individuals at increased risk for severe COVID-19 illness, including: type 1 or 2 diabetes, chronic lung disease (including moderate to severe asthma, bronchiectasis, bronchopulmonary dysplasia, chronic obstructive pulmonary disease (COPD), interstitial lung disease including idiopathic pulmonary fibrosis, pulmonary embolism, or pulmonary hypertension), cystic fibrosis, dementia, Parkinson's disease, cerebrovascular disease, chronic liver disease, chronic kidney disease (any stage), heart conditions, hemoglobin blood disorders (sickle cell disease, thalassemia).
• • 8. BMI \> 40 kg/m2
• • 9. Any potentially immune mediated disease (with the exception of well controlled hypothyroidism).
• • 10. Alcohol or drug abuse and psychiatric conditions that in the opinion of the investigator would preclude compliance with the trial or interpretation of safety or endpoint data.
• • 11. Impaired immune function or chronic infections including (but not limited to) HIV, hepatitis B or C; organ transplant; active cancer or any history of hematologic cancer; receipt of chemotherapy, radiation therapy (past 12 months) or any other potentially immunosuppressive therapy \[i.e. received oral, intramuscular or intravenous systemic immunosuppressants, or immune modifying drugs for \>14 days in total within 6 months prior to any study vaccine dose (for corticosteroids ≥ 20 mg/day of prednisone equivalent). Note: Topical medications are allowed.\], congenital immunodeficiency, anatomical or functional asplenia.
• • 12. Pregnancy or breast feeding or planned pregnancy for the duration of the study.
• • 13. Severe reactions to prior vaccination with Covid-19 mRNA vaccine or any of its components, including anaphylaxis.
• • 14. History of Guillain Barré syndrome or myopericarditis.
• • 15. Volunteers with any acute illness, including any fever (\> 100.4 F \[\> 38.0C\], regardless of the route) within 3 days prior to study entry.
• • 16. Social, occupational, or any other condition that in the opinion of the investigator might interfere with compliance with the study and vaccine evaluation.