About the Study
The purpose of this clinical trial is to measure the number of influenza cases after receiving an experimental vaccine compared with a marketed influenza vaccine.
JCCT 205
A Phase 3, Randomized, Observer-blind, Active-controlled, Case-driven
Study to Investigate the Safety, Efficacy, and Immunogenicity of
mRNA-1010 Candidate Seasonal Influenza Vaccine Compared with a
Licensed Inactivated Seasonal Influenza Vaccine in Adults ≥50 Years of
Age
50 +
/ Male or Female / Earn up to $980
Would you like to receive personalized alerts for all future opportunities – click below to join our mailing list.
Join our mailing listFrequently asked questions
View all FAQsWhat is a screening visit?
A screening visit is your first visit to our facility and takes roughly 2-4 hours. After filling out paperwork and reviewing a consent form, one of our nurses will go over the details to ensure your understanding.
This is the perfect time to ask any questions about the study and how your participation will affect you.
The nurse will then go over your medical history and take vitals.
The next step is completing a physical with our doctor. If our doctor deems you healthy enough for the study, you will then see our phlebotomist for a blood draw.
How do I prepare for my screening visit?
The night before:
- Hydrate, hydrate, hydrate!
- Avoid a large consumption of alcohol
- Avoid sugary foods and drinks
The morning of:
- Continue to hydrate well
- Eat a light, healthy breakfast (Examples: bagels, scrambled eggs, yogurt, fruit, whole grain cereal)
- Bring a photo ID
- Make sure you have a form of entertainment (Examples: Books, magazines, mobile video game systems, laptops, etc.)
What questions should I ask the nurse?
First, you can ask our nurses any questions that come to your mind at any point of the process. But some good examples are:
- Has this new medication/vaccine been tested on humans before?
- What is the purpose of this new medication/vaccination?
- What are the risks involved?
- What company developed the medication/vaccine?
- What is the procedure?
- How/What samples are collected?
- How long is the trial?
What is informed consent?
Informed consent is the process of our volunteers being given all the information about the study. For your protection, all clinical trial facilities MUST give you all the details (including risks and benefits) pertaining to the study before you give consent to volunteer. All volunteers must sign the informed consent before they can participate in a trial. As the study progresses, there could be additional informed consent forms that require your signature.
JCCT takes this process very seriously. You will be given 1 on 1 time with one of our nurses to go over the consent form and ask as many questions as you need before you sign.
Study Qualification
×Based on your response, it looks like you don’t qualify. However, we have other opportunities that you may be qualified for. Fill out the form below to join our mailing list and be informed when new opportunities are available.
