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Healthy volunteers inhale RSV virus to help fight future outbreaks

NCT ID NCT02484417

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026

Summary

This study gave healthy adults a mild dose of respiratory syncytial virus (RSV) in a controlled hospital setting to learn how the body fights the infection. Thirty-two volunteers aged 18 to 50 stayed in isolation for about 10 days while researchers monitored symptoms, viral shedding, and immune responses. The goal is to use this knowledge to develop better vaccines and treatments for RSV, which can be severe in young children and older adults.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
RSV A2 virus (intranasal inoculation)
What this could lead to
If successful, this study could help researchers develop better treatments and vaccines for RSV, which can be dangerous for children and older adults.
What could go wrong
This is an early-phase study with only 32 participants, so results may not apply broadly. The virus is expected to cause only mild cold symptoms, but unexpected reactions are possible.

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 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

32 people

The number who actually took part.

Started

Jul 2015

Finished

Aug 2016

Lead sponsor

A government research agency

The lead sponsor is the US National Institutes of Health.

Who can take part

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

Ages

18 to 50 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: 1. Age 18-50 years. 2. General good health, without significant medical illness, physical exam findings, or significant laboratory abnormalities as determined by the investigator. 3. Willingness to stay confined to the inpatient unit for required study duration. 4. Willingness to have samples stored for future research. 5. Subjects must be of non-childbearing potential (i.e., either surgically sterilized \[bilateral oophorectomy, bilateral tubal ligation, hysterectomy\] or, if of child-bearing potential and sexually active with a partner who can get them pregnant, then they must be have in place an effective method of contraception for at least 30 days prior to administration of the challenge virus and until 30 days after challenge virus administration: * intrauterine device (IUD) or equivalent * hormonal contraceptives (e.g., consistent, continuous use of contraceptive pill, patch, ring, implant or injection) * if participant uses contraceptive pill, patch or ring, two methods of contraception are required; a barrier method is to be used at the time of potentially reproductive sexual activity (e.g. male/female condom, cap, or diaphragm plus spermicide) * be in a monogamous relationship with a partner who has undergone a vasectomy at least 6 months prior to first dose of study agent. EXCLUSION CRITERIA: The presence of any one of the following criteria is sufficient to exclude a prospective subject from enrolling in this study: 1. Female subject is pregnant or lactating OR planning to become pregnant in the timeframe that begins 30 days prior to the inoculation and ends 30 days after inoculation. 2. Evidence of clinically significant neurologic, cardiac, pulmonary, hepatic, hematologic, rheumatologic, endocrine, autoimmune, or renal disease. 3. Complete blood count (CBC), AST, ALT, or creatinine values are both outside of the NIH Department of Laboratory Medicine normal reference range and deemed clinically significant by the PI. 4. Behavioral or cognitive impairment or psychiatric disease that in the opinion of the investigator affects the ability of the subject to understand and cooperate with the study protocol. 5. A medical, occupational, or family problem as a result of alcohol or illicit drug use during the past 12 months. 6. Routine smoker of a tobacco product or marijuana currently or in the past year. 7. Current alcohol abuse or addiction. 8. Current illicit drug abuse or addiction. 9. Presence of any febrile illness or symptoms suggestive of a viral respiratory infection within 2 weeks prior to inoculation accompanied by a positive multiplex FilmArray PCR performed on nasal wash. 10. Use of corticosteroids (including nasal preparations) or immunosuppressive drugs within 30 days before inoculation. 11. A history of asthma within the past 10 years, or a current diagnosis of asthma or reactive airway disease associated with exercise, seasonal hay fever or allergic rhinitis. 12. Positive FDA-approved HIV test result prior to inoculation. 13. Positive serology for hepatitis C virus within 6 months prior to inoculation. 14. Presence of hepatitis B surface antigen within 6 months prior to inoculation. 15. A known immunodeficiency syndrome. 16. Receipt of a licensed vaccine within 4 weeks prior to viral inoculation. 17. Receipt of blood or blood-derived products (including immunoglobulin) within 6 months prior to viral inoculation. Receipt of packed red blood cells given for an emergent indication in an otherwise healthy person, and not required as ongoing treatment is not exclusionary (for example packed red blood cells emergently given during an elective surgery). 18. Receipt of another investigational agent within 3 months prior to viral inoculation. 19. Individual with body mass index (BMI) less than or equal to 18.5 or greater than or equal to 37.5. 20. Any significant abnormality of the nose or nasopharynx, including recurrent epistaxis within 3 months prior to viral inoculation. 21. Nasal or sinus surgery within 6 months prior to viral inoculation. 22. Shares household, works closely with, or has routine contact with a child (children) \< 5 years of age or with immunocompromised individual(s), adults with significant cardiopulmonary disease, persons with significant asthma, institutionalized elderly or elderly with functional disability or any other individual that, in the judgment of the PI, might be at increased risk for complications if exposed to RSV. 23. Deprived of freedom by an administrative or court order or in an emergency setting. 24. Any condition that in the opinion of the principal investigator (PI) would jeopardize the safety or rights of a person participating in the trial or would render the person unable to comply with the protocol.

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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

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

More trials for these conditions

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