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Scientists dive deep into RSV vaccine immune secrets

NCT ID NCT07185399

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times

Summary

This study looks at how the RSV vaccine affects the immune system in adults aged 60 and older. Researchers will take blood samples before and after vaccination to find early signs of protection. The goal is to understand why some people respond better than others. 14 volunteers will be followed for 6 months.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

14 people

The number who actually took part.

Started

Oct 2025

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

60 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults ≥60 years of age at the time of enrollment. * Able and willing to provide written informed consent. * Eligible for receipt of an FDA-approved RSV vaccine (MRESVIA) per Advisory Committee on Immunization Practices (ACIP)/Centers for Disease Control and Prevention (CDC) guidelines. * Available for all study visits and procedures, including follow-up through Day 365. * Willing to allow access to prior RSV vaccination history (if applicable) for eligibility verification Exclusion Criteria: * History of severe allergic reaction (e.g., anaphylaxis) to any prior vaccines or any component of the MRESVIA vaccine, including polyethylene glycol (PEG), the amino lipid SM-102 (SM-102), or other listed excipients. * Acute illness or fever (temperature ≥100.4°F) at the time of vaccination (participant may be rescheduled). * Immunocompromising conditions, including: * Current cancer chemotherapy or immunosuppressive therapy. * History of hematologic malignancies or other immune-mediated diseases that would interfere with vaccine response. * Known or suspected HIV infection with cluster of differentiation 4 (CD4) count \<200 or uncontrolled viremia. * Clinically significant cardiac, pulmonary, renal, hepatic, or neurological disease that, in the opinion of the investigator, would preclude participation or confound interpretation of immune data. * Uncontrolled autoimmune disorder. * Current use of systemic corticosteroids equivalent to ≥20 mg prednisone daily for more than 14 consecutive days in the past month. * History of Guillain-Barré Syndrome or other demyelinating neurological disorders. * History of myocarditis, pericarditis, or myopericarditis within the last 2 months. * Any bleeding disorder that poses a risk for venipuncture or vaccination complications. * Participation in another clinical trial involving an investigational agent within 30 days of enrollment. * Receipt or plan receipt of vaccines in the past an upcoming 28 days. * Prior receipt of any RSV vaccine. * Receipt of blood products or immune globulin within the prior 3 months. * History of excessive alcohol consumption or drug use, or psychiatric/social/occupational conditions that may interfere with study compliance. * Any other condition that, in the opinion of the investigator, may interfere with study conduct or participant safety.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • The Hope Clinic of the Emory Vaccine Center

    Decatur, Georgia, 30030, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.