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Can the RSV vaccine protect the most vulnerable? new study aims to find out

NCT ID NCT07296120

First seen Jan 08, 2026 · Last updated Jun 23, 2026 · Updated 28 times

Summary

This study tests whether the RSV vaccine Abrysvo can help blood cancer patients who have had a stem cell transplant or CAR-T therapy build immunity against RSV. Researchers will measure antibody levels before and after vaccination in 30 adults. The goal is to see if the vaccine triggers a strong enough immune response to prevent serious respiratory infections.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • Cooper University Hospital

    Camden, New Jersey, 08103, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

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

Active substance

Respiratory Syncytial Virus Prefusion F Vaccine (RSVpreF, brand name Abrysvo)

What this could lead to

If it works, this could show that the RSV vaccine protects vulnerable blood cancer patients from severe respiratory infections after transplant or CAR-T therapy.

What could go wrong

This is a small, early-phase study with only 30 participants, so results may not apply to everyone. The vaccine may not produce a strong immune response in these patients due to their weakened immune systems.

Conditions

The condition(s) this trial relates to.

hematopoietic and lymphoid cell neoplasm hematopoietic and lymphoid system neoplasm respiratory syncytial virus infectious disease prevention target

As listed by the trial registrant

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