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Could CAR t cells tame severe vasculitis without lifelong drugs?

NCT ID NCT07388277

First seen Feb 05, 2026 · Last updated Jun 23, 2026 · Updated 21 times

Summary

This early-phase trial tests a new treatment called CC-97540, which uses a patient's own immune cells engineered to target and destroy harmful B cells. It is for 12 adults with severe ANCA-associated vasculitis that has not responded to standard therapies. The main goals are to check safety and see if it can lead to remission without needing ongoing immune-suppressing medication.

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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: •••••@•••••

  • Contact

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

Locations

  • Massachusetts General Hospital

    RECRUITING

    Boston, Massachusetts, 02114, United States

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

    Contact

What this could mean

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

Active substance

CC-97540 (CAR T cells targeting CD19) plus lymphodepletion chemotherapy

What this could lead to

If it works, this could point toward a treatment that puts severe vasculitis into long-term remission without needing lifelong immune-suppressing drugs.

What could go wrong

This is a very early, small trial (12 people) focused on safety. CAR T cells can cause serious side effects like cytokine release syndrome, and it may not work or may not lead to lasting remission.

Conditions

The condition(s) this trial relates to.

anti-neutrophil cytoplasmic antibody-associated vasculitis

As listed by the trial registrant

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