Maternal RSV Vaccine Study

• Now Open in Grand Island, Hastings, and Norfolk, NE; and Johnson City, NY

Respiratory syncytial virus (RSV) is the leading cause of lung infection (like bronchiolitis and viral pneumonia) for infants, and can be life-threating. In the U.S., RSV is the leading cause of infant hospitalization. Pregnant women may be eligible to receive an investigational RSV vaccine through a clinical study. This vaccine is being studied to determine if it can prevent RSV illnesses in infants after they’re born by vaccinating their mothers during the pregnancy.

Eligible participants…

Must be pregnant and aged 18 to 49
Must be between 24 and 34 weeks of gestation when they get the study injection
Must have a low-risk pregnancy, and be at no known increased risk for complications
May receive compensation for time and travel
May receive the investigational vaccine or a non-active placebo
Do not need insurance to join this study
Receive study-related care and exams at no cost

For more information, complete the form on this page. After you submit your information, a Meridian enrollment specialist will call you to talk about the study. There is no obligation to join — you can decide if the study is right for you.

You can also talk to a Meridian enrollment specialist about this study by calling (402) 934-7563 (NE) or (912) 623-2240 (NY).

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Study Locations

Nebraska (Grand Island): Meridian Clinical Research, 2444 West Faidley Avenue, Grand Island, Nebraska 68803
Nebraska (Hastings): Meridian Clinical Research, 2115 N. Kansas Ave., Hastings, NE 68901
Nebraska (Norfolk): Meridian Clinical Research, 1410 N 13th St, Suite 5, Norfolk, NE 68701
New York (Johnson City): Meridian Clinical Research, 355 Main Street, Johnson City, NY 13790

More information about this study...

After you submit your information, a Meridian enrollment specialist will contact you.

Participating in a study is an important decision — we’re here to help you before, during, and after studies.

Please note: Health insurance is NOT required to join.

Will I benefit from this study?

You are not guaranteed to benefit from being in a clinical study. However, information gathered in this study may help uncover better ways to treat condition(s) for you and others worldwide.

Is participation voluntary after I submit my information?

Yes. Participation in a study is entirely voluntary. In the informed consent process, you’ll learn about the product being studied, your role in the trial, potential side effects, tests that will be performed, and the number of visits required. You will need to sign an informed consent form to join the study only after you fully understand your role in the study.

Will I get a physical exam?

If you join the study, you will receive a physical exam. You may also receive specific exams or tests — the results of which will be shared with you.

Will I receive compensation?

While participation in a clinical study is voluntary, you may be reimbursed for your study-related travel and expenses. After you submit your information, a Meridian enrollment specialist will call you to talk about the study. Staff at the research clinic will discuss possible reimbursement with you.

Founded in 1999 in Omaha, NE, Meridian studies the safety and effectiveness of new medicines, devices, and treatments. Its mission is to enrich lives by providing quality, compassionate care to patients and unparalleled clinical research services. Clinical studies help scientists develop life-changing medicines, but it starts with you — participation makes it all possible. For more than 20 years, thousands of patients have trusted Meridian because of our focus on creating a positive patient experience.

Maternal RSV Vaccine Study

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